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DOI: 10.1039/D0RA01050B (Review Article) RSC Adv., 2020, 10, 11463-11474

Traditional uses, phytochemistry, pharmacology and toxicology of Lamiophlomis rotata (Benth.) Kudo: a review

Zhan-Hu Cui† ab, Shuang-Shuang Qin†a, Er-Huan Zangc, Chao Lid, Li Gaod, Quan-Chao Lie, Yun-Long Wange, Xian-Zhang Huang*d, Zhong-Yi Zhang*ab and Min-Hui Li*acfgh
aGuangxi Botanical Garden of Medicinal Plants, Nanning, Guangxi 530023, China. E-mail: prof_liminhui@yeah.net
bFujian Agriculture and Forestry University, Fuzhou, Fujian 350002, China. E-mail: zyzhang@fafu.edu.cn
cBaotou Medical College, Baotou, Inner Mongolia 014060, China
dNanyang Institute of Technology, Nanyang, Henan 473004, China. E-mail: hxzgreat@163.com
eThe First People's Hospital of Nanyang Affiliated to Henan University, Nanyang, Henan 473010, China
fInner Mongolia Medical University, Hohhot, Inner Mongolia 010110, China
gInner Mongolia Key Laboratory of Characteristic Geoherbs Resources and Utilization, Baotou Medical College, Baotou, Inner Mongolia 014060, China
hInner Mongolia Institute of Traditional Chinese Medicine, Hohhot, Inner Mongolia 010020, China

Received 4th February 2020 , Accepted 8th March 2020

First published on 20th March 2020

Abstract

Lamiophlomis rotata (Benth.) Kudo is a herbaceous plant of the family Lamiaceae, subfamily Lamioideae. Approximately, 127 chemical constituents have been isolated and identified from L. rotata, including iridoids, flavonoids, phenylethanoid glycosides, polysaccharides, and organic acids. These chemical constituents have extensive pharmacological properties, which include anti-nociceptive, haemostatic, anti-inflammatory, anti-tumour, immunomodulatory, antioxidant, and cardio-protective activities. Documentation of its historical use in traditional medicine and contemporary phytochemical and pharmacological research indicate that L. rotata has significant potential in therapeutic and health care applications. Both whole extracts and individual chemical components isolated from this plant exhibit a wide range of biological activities that warrant further investigation. These investigations can be assisted by careful review of existing traditional knowledge from diverse cultural backgrounds. A new search for chemical and biological markers and reinforced protection of the germplasm resources of L. rotata are also important to ensure targeted and sustainable use of this medicinal resource. The aim of this review was to provide comprehensive information on the botanical characteristics, traditional uses, ethnopharmacology, chemical and pharmacological properties, toxicity profile, and conservation status of L. rotata, to improve understanding of its mechanisms of action so that novel therapeutic agents may be developed from this plant.

1. Introduction

Lamiophlomis rotata (Benth.) Kudo is a herbaceous plant in the family Lamiaceae, subfamily Lamioideae.1 Lamiophlomis is a monotypic genus, represented by L. rotata. There are significant differences in the chemical constituents in plants between the genera Lamiophlomis and Phlomis, therefore, the genus Lamiophlomis, which was originally assigned to the genus Phlomis, was later re-assigned.2 The formal Chinese name of L. rotata is Duyiwei (image file: d0ra01050b-u1.tif), or Dubutong (image file: d0ra01050b-u2.tif) in Chinese dialect.3,4 L. rotata is also known as Daba, Gaguola or Dabuba in Tibetan folk medicine,4 and as Dabage or Dagama in traditional Mongolian medicine. This herb has been widely used as a traditional Tibetan medicine, traditional Mongolian medicine, and traditional Chinese medicine for thousands of years.3 It is well known for treating traumatic injury, traumatic haemorrhage and rheumatic arthralgia, as well as diabetes resulting from haemostatic imbalances. The phytochemical and pharmacological studies of the genus Lamiophlomis have drawn much attention since 1987. Thus far, the compounds isolated from L. rotata have included iridoids, flavonoids, phenylethanoid glycosides, polysaccharides, and organic acids. Modern pharmacological studies have demonstrated that these compounds possess anti-nociceptive, haemostatic, anti-inflammatory, anti-tumour, immunomodulatory, cardio-protective, anti-bacterial, antioxidant, anti-fatigue, anti-ulcer, and memory-boosting activities.5–11

The aim of the review was to provide comprehensive information on the botanical characteristics, distribution, traditional uses, ethnopharmacology, chemical constituents, pharmacological activities, and toxicity profile of L. rotata, gained from both historical and recent publications. It is hoped that this compiled body of knowledge will provide a strong foundation for further studies on the mechanisms of action of this medicinal plant, and guide the development of novel therapeutic agents.

2. Botanical characterisation and distribution

L. rotata is a perennial herbaceous plant which is erect, with horizontally thickened rhizomes, that grows to 2.5–10 cm in height and 0.5–1.1 cm wide. Its leaves are diamond-shaped and decussate, and they grow up to 6–13 cm long and 7–12 cm wide. The leaf apex can be obtuse, rounded or acute. The leaves have crenate leaf margins. The cymes are densely arranged in a short-scabbed head shape or spike-like inflorescences of 3.5–7 cm in length. The bracts are lanceolate, oblanceolate or linear, and grow to 1–4 cm long and 1.5–6 mm wide. The calyx is tubular, approximately 10 mm in length and 2.5 mm in width, and is pubescent along the external veins. The corolla is tube-shaped and about 1.2 cm long; puberulent on the outside and more densely puberulent within the middle of the tube. The flowering-fruiting season (in the northern hemisphere) for L. rotata is from June to September. The representative pictures of L. rotata are shown in Fig. 1.
image file: d0ra01050b-f1.tif
Fig. 1 L. rotata from Jingzhubencao (Qing Dynasty, AD 1848) (A), the aerial parts of L. rotata (B), and Lamiophlomis herba (C).

L. rotata is mainly distributed in China, Nepal, Sikkim and Bhutan, where they grow wild on the meadows or hills, at 2700 to 4500 metres above sea level.1 In China, L. rotata is mainly found in the western regions such as Gansu, Qinghai, Sichuan, Yunnan, and the Tibet provinces/autonomous regions. Among them, Tibet and the Maqu county of Gansu are the main growing areas of L. rotata, and it is here that high quality medicinal material is produced.4

3. Traditional uses and ethnopharmacology

L. rotata has been used in traditional Tibetan medicine for more than a thousand years, with significantly therapeutic effects described for traumatic injury, traumatic haemorrhage and rheumatic arthralgia, as well as for diabetes resulting from haemostatic imbalances. In traditional Tibetan medicine, L. rotata is described to exert its curative functions by promoting blood circulation, relieving swelling and pain, and removing blood stasis. The earliest record of L. rotata use in China appeared in the Yuewangyaozhen (AD 700), where it was used for marrow supplementation and yellow water after the oedema treatment.4 Later, its use was recorded in famous medicinal writings, including the Sibuyidian (AD 765), where its functions, usage and compatibility with other medications were considered.4 A detailed and systematic description of the ecological environment of L. rotata and its morphology was recorded in as early as 1848, in the Jingzhubencao (Qing Dynasty, AD 1848). In 1978, L. rotata was included in the local standards of Tibetan medicine in six provinces (Tibet, Qinghai, Sichuan, Gansu, Yunnan and Xinjiang). In 1995, the Ministry of Health included it in the Pharmaceutical Standards of the Ministry of Health of the People's Republic of China (volume 1).

In order to improve its clinical efficacy, L. rotata is also prescribed as a critical ingredient in combination with other Chinese herbs such as Curcuma longa, Salvia miltiorrhiza, and Pyrrosia lingua (Table 1).

Table 1 Traditional medicine uses of L. rotata in Chinaa
Preparation names Compositions Traditional and clinical uses Origins
a All the names of crude drug in column are identified properly according to Chinese Pharmacopoeia 2015.
Duyiwei pian Lamiophlomis herba 1000 g Treatment of analgesia, fracture, hemostasis, sprain, rheumatism, arthralgia pain, metrorrhagia, dysmenorrhea, painful gum Chinese Pharmacopoeia 2015
Duyiwei capsule Lamiophlomis herba 1000 g Treatment of analgesia, fracture, hemostasis, sprain, rheumatism, arthralgia pain, metrorrhagia, dysmenorrhea, painful gum Chinese Pharmacopoeia 2015
Xiaotong plaster Lamiophlomis herba, Curcumae longae rhizoma, Bubalus bubalis Linnaeus, etc Treatment of sprain, hyperosteogeny, periarthritis, strain of lumbar muscles Chinese Pharmacopoeia 2015
Dabage plaster Lamiophlomis herba, Salviae miltiorrhizae Radix et Rhizoma, and Pyrrosiae folium, etc. Treatment of traumatic injury Mongolian pharmacy17
Wuyang powder Lamiophlomis herba, Fel Ursi, etc Treatment of traumatic injury. Detumescence, acesodyne Mongolian pharmacy17

In traditional Chinese medicine, L. rotata has a long history of use in treating injuries from falls, muscle and bone pain, joint swelling and pain, dysmenorrhea, metrorrhagia.4 For instance, it was recorded in the Sichuanzhongyaozhi that L. rotata had been used to treat injuries from falls, muscle pain, joint swelling and pain, dysmenorrhea, and metrorrhagia.12 Lamiophlomis originates from the root, rhizome or whole herb of L. rotata (recorded in the Zhonghuabencao13). Its early collection for use as a traditional Chinese medicine is documented in the Chinese Pharmacopoeia (2000). Since then, L. rotata has also been recorded to have significant therapeutic effects in traumatic injury, traumatic haemorrhage and rheumatic arthralgia in the Chinese Pharmacopoeia (2015).14 Generally, L. rotata is used directly in the clinic without any prior processing, and commonly for pain relief. However, processing the herb in vinegar and wine may increasing its flavonoid content and enhance its analgesic effects.15,16

In traditional Mongolian medicine, there are only a few records of L. rotata usage, where L. rotata was described to remedy analgesia, detumescence, traumatic injury, and promote wound healing and porosis in a process known as removing “Huangshui”.17

4. Phytochemistry

Phytochemical investigations of L. rotata have led to the isolation of 127 compounds, including iridoids, flavonoids, phenylpropanoid glucosides, polysaccharides, and organic acids.27,34,42 These structures are shown in Fig. 2–10.
image file: d0ra01050b-f2.tif
Fig. 2 The skeletal structures of iridoids from L. rotata.

image file: d0ra01050b-f3.tif
Fig. 3 The structures of compounds 32–47 from L. rotata.

4.1 Iridoids

The main compounds isolated from the aerial regions and rhizomes of L. rotata are iridoids (Table 2). To date, 47 iridoids have been isolated. Li et al. showed that the main substance responsible for the analgesic effect of L. rotata was iridoid glycosides.18–20 The simple compounds 8-O-acetyl shanzhiside methyl ester (1), shanzhiside methyl ester (2), loganin (23), and phloyoside II (38) were detected in total iridoid glycosides, and could significantly inhibit foot pain and swelling caused by acetic acid. Yi et al.21 isolated an additional four iridoid glycosides from an n-butanol extract from the rhizomes of L. rotata in 1997, and identified these as 8-O-acetyl shanzhiside methyl ester (1), 6-O-acetyl shanzhiside methylester (4), penstemoside (5), and 7,8-dehydropenstemoside (35) by spectral analysis and chemical methods. A further ten iridoid glycosides components were identified by four independent groups in ethanol extracts of L. rotata. These include sesamoside (3), 6′-O-β-D-glucopyranosylphlorigidoside C (8), 6′-O-α-D-galactopyranosylphlorigidoside C (9), 6′-O-β-D-glucopyranosylsesamoside (10), 6′-O-α-D-galactopyranosylsesamoside (11), phlorigidoside C (12), 6′-O-β-D-glucopyranosylbarlerin (13), 6′-O-α-D-galactopyranosylbarlerin (14), 6′-O-α-D-galactopyranosylshanzhiside methyl ester (15), and shanzhisin methyl ester gentiobioside (16).27,28,34,41 More recently, in 2018, Zhang et al.24 isolated three new iridoid glycosides from L. rotata, namely, barlerin-6′′-hydroxy-2′′,6′′-dimethylocta-2′′,7′′-dienate ester (27), 7-dehydroxy-zaluzioside (33), and 6β-n-butoxy-7,8-dehydropenstemonoside (34). Their structures were characterised by high-resolution mass spectrometry, and one-dimensional and two-dimensional nuclear magnetic resonance (NMR) spectroscopy. It was found that 6β-n-butoxy-7,8-dehydropenstemonoside (34) and 8-epi-7-deoxy-loganin (25), and 7,8-dehydropenstemonoside (36) significantly inhibited NF-κB activation upon lipopolysaccharide stimulation.22,23 In 1990, Yi et al.25 separated lamiophlomiol A (39) and lamiophlomiol B (6) from the ethanol extracts from the rhizomes of L. rotata. This was followed by identification of lamiophlomiol C (7) in 1992.26 The structures of the three lamiophlomiols are similar. They all have epoxy structures at the C-7 and C-8 sites of the iridoid skeleton. Lamiophlomiol A (39) and lamiophlomiol B (6) are isomeric and cannot be completely separated but their structures were confirmed by spectroscopy and chemical analysis. Twelve compounds 6′-O-syringyl-deoxysesamoside (17), 5-deoxysesamoside (18), phlomiol (19), lamalbid (20), schismoside (21), chlorotuberoside (22), 7-epi-loganin (24), 5-hydroxy-loganin (26), 6-O-syingyl-barlerin (28), 5-deoxypulchelloside I (29), 5-desoxylamiide (30), and deoxypulchelloside I (31) have also been identified in L. rotata.22–24 Ethanol extracts from the rhizomes of L. rotata have also been shown to contain 6α-dihydrocornic methyl ester-6′-O-β-D-glucopyranoside (32) and 7,8-dehydropenstemoside (35),22,23 as well as phloyoside I (37), phloyoside II (38), 7,8-dehydropenstemoside (40), and gentioside (44). In 2015, researchers focusing on the aerial region of L. rotata by silica gel, MCI chromatography and gel chromatography, preparative thin layer chromatography, preparative high-performance liquid chromatography and recrystallisation, further identified lamiophlomiol D (41), lamiophlomiol E (42), and lamiophlomiol F (43). Loganic acid (45), 8-O-acetylshanzhiside (46), 10-methylixoside (47) from L. rotata and confirmed these structures by 1H-NMR and 13C-NMR spectral data.24–30
Table 2 Iridoids isolated from L. rotata (1–31)
No. Name Skeletons R1 R2 R3 R4
1 8-O-Acetyl shanzhiside methyl ester I OH H OCOMe —
2 Shanzhiside methyl ester I OCOMe H OH —
3 Sesamoside II OGlc OH — —
4 6-O-Acetyl shanzhiside methyl ester I OH H OH —
5 Penstemoside VI α-OH α-OH H β-Me
6 Lamiophlomiol B II H OH — —
7 Lamiophlomiol C II OH OH — —
8 6′-O-β-D-Glucopyranosylphlorigidoside C III H β-D-Glc α-OH —
9 6′-O-α-D-Galactopyranosylphlorigidoside C III H α-D-Gal α-OH —
10 6′-O-β-D-Glucopyranosylsesamoside III OH β-D-Glc α-OH —
11 6′-O-α-D-Galactopyranosylsesamoside III OH α-D-Gal α-OH —
12 Phlorigidoside C III H H α-OH —
13 6′-O-β-D-Glucopyranosylbarlerin IV Ac β-D-Glc — —
14 6′-O-α-D-galactopyranosylbarlerin IV Ac α-D-Gal — —
15 6′-O-α-D-Galactopyranosylshanzhiside methyl ester IV H α-D-Gal — —
16 Shanzhisin methyl ester gentiobioside IV OH β-D-Glc — —
17 6′-O-Syringyl-deoxysesamoside III H Syringyl β-OH —
18 5-Deoxysesamoside III H H β-OH —
19 Phlomiol V OH β-OH α-Me β-OH
20 Lamalbid V H β-OH α-Me β-OH
21 Schismoside V H β-OH α-OH β-Me
22 Chlorotuberoside V H α-Cl α-Me β-OH
23 Loganin VI H H β-OH β-Me
24 7-epi-Loganin VI H H α-OH β-Me
25 8-epi-7-Deoxyloganin VI H H H α-Me
26 5-Hydroxy-loganin VI OH H β-OH β-Me
27 Barlerin-6′′-hydroxy-2′′,6′′-dimethylocta-2′′,7′′-dienate ester I O-a H Acetyl —
28 6-O-Syingyl-barlerin I O-Syingyl H Acetyl —
29 5-Deoxypulchelloside I VI H α-OH α-OH β-Me
30 5-Desoxylamiide I H β-OH β-OH —
31 Deoxypulchelloside I I β-OH β-OH H —

Among the iridoids, 8-O-acetyl shanzhiside methylester (1), shanzhiside methyl ester (2) and 6-O-acetyl shanzhiside methyl ester (4) were detected at higher concentrations compared to the other components in L. rotata. Both shanzhiside methyl ester and 8-O-acetyl shanzhiside methyl ester have been used as a quality control indicators of L. rotata content in the Pharmacopoeia of P. R. China (2015).3

4.2 Flavonoids

The flavonoids can be classified by their skeletal structures into apigenin, luteolin and quercetin [2] (Fig. 4). Through silica gel column and polyamide column chromatography, followed by the hydrochloric acid-magnesium powder reaction test and spectral data analyses, Zhang et al. identified five flavonoids in ethanol extracts from the aerial regions of L. rotata, namely, luteolin (48), luteolin-7-O-glucoside (49), quercetin (50), quercetin-3-O-glucoside (51), and apigenin-7-O-neohesperidoside (52).31 Three flavonoid glycosides, luteolin-7-O-β-D-glucopyranoside (53), apigenin-7-O-β-D-glucopyranoside (54), and luteolin-7-O-(6′′-O-β-D-apiofuranosyl)-β-D-glucopyranoside (55) have also been identified in n-butanol extracts of L. rotata, and this is the first report of the isolation of this family of compounds from L. rotata.32
image file: d0ra01050b-f4.tif
Fig. 4 The skelectal structures of flavonoids from L. rotata.

image file: d0ra01050b-f5.tif
Fig. 5 The structures of compounds 69–70 from L. rotata.

image file: d0ra01050b-f6.tif
Fig. 6 The skeletal structures of phenylethanoid glycosides from L. rotata.

image file: d0ra01050b-f7.tif
Fig. 7 The structures of compounds 81–87 from L. rotata.

image file: d0ra01050b-f8.tif
Fig. 8 The structures of compounds 88–99 from L. rotata.

image file: d0ra01050b-f9.tif
Fig. 9 The structures of compounds 100–113 from L. rotata.

image file: d0ra01050b-f10.tif
Fig. 10 The structures of compounds 114–127 from L. rotata.

A further seven flavonoids have been isolated and identified from the 70% ethanol extracts of L. rotata, including apigenin-7-O-β-D-(6′′-p-coumaroyl)-glucopyranoside (56) apigenin (57), apigenin-7-O-(6′′-O-β-D-apiofuranosyl)-β-D-glucopyranoside (58), 4′-(p-carbonylphenyl)-luteolin (59), luteolin-7-O-β-D-(6′′-O-acetyl)-glucopyranoside (60), apigenin-7-O-β-D-(6′′-O-p-E-coumaroyl)-glucopyranoside (61), and apigenin-7-O-β-D-(4′′,6′′-di-O-p-E-coumaroyl)-glucopyranoside (62).33

Among these flavonoids, apigenin-7-O-β-D-glucopyranoside, luteolin-7-O-β-D-glucopyranoside and luteolin-7-O-(6′′-O-β-D-apiofuranosyl)-β-D-glucopyranoside were found in higher concentrations compared to the other components.34 Using high performance liquid chromatography-electrospray/quadrupole time-of-flight tandem mass spectrometry (UPLC-ESI-TOF MS) identified rutin (63) in L. rotata.35

In 2008, Li et al.36 studied the chemical constituents of ethanol extracts from the aerial regions of L. rotata, and confirmed the structure of the following flavonoids by chemical and spectral methods (Table 3): luteolin (48), apigenin-7-O-(6′′-(E)-p-coumaroyl)-β-D-galactopyranoside (64), tricin (65), acacetin (66), and genkwanin (67). Luteolin (48) and tricin (65) profoundly inhibit the release of nitric oxide (NO) by murine macrophages, which may account for the anti-inflammatory activity of L. rotata. Finally, isorhamnetin (68) and icariin (69) were identified in the ethanol extract of L. rotata in 2008 whilst 1-hydroxy-2,3,5-trimethoxyxanthone (70) was identified in the polyethylene-soluble fraction of the ethanol extract.37

Table 3 Flavonoids isolated from L. rotata (48–68)
No. Name Skeletons R1 R2 R3 R4 R5
48 Luteolin I H H H OH H
49 Luteolin 7-O-glucoside I H H OGlc OH H
50 Quercetin I H OH OH OH H
51 Quercetin-3-O-glucoside I H OGlc OH OH H
52 Apigenin-7-O-neohesperidoside I Neohesp H H OH H
53 Luteolin-7-O-β-D-glucopyranoside I Glc H OH OH H
54 Apigenin-7-O-β-D-glucopyranoside I Glc H H OH H
55 Luteolin-7-O-(6′′-O-β-D-apiofuranosyl)- β-D-glucopyranoside I Api–Glc H OH OH H
56 Apigenin-7-O-β-D-(-6′′-p-coumaroyl)-glucopyranoside II H p-Coumaroyl — — —
57 Apigenin I H H H OH H
58 Apigenin-7-O-(6′′-O-β-D-apiofuranosyl)-β-D-glucopyranoside I Glc–Api H H OH H
59 4′-(p-Carbonylphenyl)-luteolin I H H O-p-Carbonylphenyl OH H
60 Luteolin-7-O-β-D-(6′′-O-acetyl)-glucopyranoside I Acetyl-Glc H OH OH H
61 Apigenin-7-O-β-D-(6′′-O-p-E- coumaroyl)-glucopyranoside II H p-E-Coumaroyl — — —
62 Apigenin-7-O-β-D-(4′′,6′′-di-O-p-E-coumaroyl)-glucopyranoside II p-E-Coumaroyl p-E-Coumaroyl — — —
63 Rutin I H Rha–Glc OH OH H
64 Apigenin7-O-(6′′-(E)-p-coumaroyl)-β-D-galactopyranoside I Gal H p-Coumaroyl OH H
65 Tricin I H H OMe OH OMe
66 Acacetin I H H H OMe H
67 Genkwanin I Me H H OH H
68 Isorhamnetin I H OH OMe OH H

4.3 Phenylethanoid glycosides

Seventeen phenylethanoid glycosides (71-87) have been isolated and identified from L. rotata (Table 4). Lamiophlomioside A (72), cistanoside C (73), 6′-β-D-apiofuranosyl cistanoside C (74), and cis-lamiophlomiside A (75) were identified in the n-buthanol extracts of both the rhizomes and aerial regions of L. rotata.32,34–40 Leucosceptoside B (71), alyssonoside (79), and isoverbascoside (86) were isolated and purified from L. rotata by high-speed counter-current chromatography combined with macroporous resin (MR) column separation. Wang et al.32 used electrospray mass spectrometry (ESI-MS), 1H-NMR, 13C-NMR and other modern spectroscopy methods to isolate and identify three phenylethanol glycosides in the n-butanol extract from the rhizomes and aerial region of L. rotata, namely, forsythoside B (76), betonyosides A (77), and verbascoside (78).
Table 4 Phenylethanoid glycosides isolated from L. rotata (71–80)
No. Name R1 R2 R3 R4 R5 αβ moiety
71 Leucosceptoside B OH OMe H OApi OMe E
72 Lamiophlomioside A OMe OH H OApi OMe E
73 Cistanoside C OMe OH H OH OH E
74 6′-β-D-Apiofuranosyl cistanoside C OMe OH H OApi OH E
75 cis-Lamiophlomiside A OMe OH H OApi OMe Z
76 Forsythoside B OH OH H OApi OH E
77 Betonyosides A OH OH OH OH OMe E
78 Verbascoside OH OH H OH OH E
79 Alyssonoside OH OH H OApi OMe E
80 Campneoside II OH OH OH OH OH E

A further six phenylethanoid glycosides have been isolated and identified in the 70% ethanol extracts of L. rotata by spectral analyses, including via UV, IR, MS, 1H-NMR, 13C-NMR and 2D-NMR. These include campneoside II (80), decaffeoylverbascoside (81), cistanoside E (82), betonyoside B (83), betonyoside C (84), and cistanoside F (85).34 Most recently, Pan et al.29 isolated and purified 50% ethanol extracts from L. rotata by silica gel, Ozone-Depleting Substances (ODS), and sephadex LH-20, and isolated markhamioside A (87) from L. rotata for the first time in 2018.

4.4 Polysaccharides

The eleven main polysaccharides identified in L. rotata include salviifoside A (88), vanillyl-O-β-D-glucopyranside (89), icariside H1 (90), n-butyl-β-D-fructopyranoside (91), eugenyl-O-β-D-glucopyranoside (92), 5β,6α-dihydroxy-3β-(β-D-glucoyranosyloxy)-7-megastigmen-9-one (93), n-butyl-β-D-fructofuranoside (94), (±)-α-terpineol-8-O-β-D-glucopyranoside (95), (2Z)-2,6-dimethyl-6-hydroxyocta-2,7-dienyl-O-β-D-glucopyranoside (96), β-D-glucopyranoside-(2→1)-β-D-glucopyranoside (97), and (Z)-3-hexenyl glucopyranoside (98). These were identified by UV, infrared, MS, 1H-NMR, 13C-NMR, 2D-NMR and other spectral analysis techniques in ethanol extracts of the aerial regions of L. rotata.34 Mei et al.42 used silica gel, MCI chromatography, and preparative HPLC to study extracts from the aerial regions of L. rotata and by analysing the physical and chemical properties and spectral data, isolated salidroside (99) for the first time in 2014. This compound is likely to contribute to the anti-fatigue and anti-oxidative damage properties of L. rotata.30,42

4.5 Organic acids

Fourteen organic acids (100–113) have been isolated and identified from L. rotata. Zhang et al.34 isolated and identified the first four organic acid compounds from the aerial regions of L. rotata, namely, oleanolic acid (100), 4-hydroxybenzoic acid (101), caffeic acid (102), and (7E,10E,13E)-hexadeca-7,10,13-trienoic acid (103). Zhang et al.33 studied the chemical constituents in the ethanol fraction of L. rotata, and according to their physical and chemical properties and spectral data analyses, identified syringic acid (104) and 3,4-dihydroxybenzoic acid (105) in 2011. Mei et al.42 isolated three additional organic acid compounds from the ethanol fraction of L. rotata, namely, (E)-4-hydroxyhex-2-enoic acid (106), cis-2,4,5-trihydroxycinnamic acid (107), and 2,5-dihydroxy-benzoic acid (108). In 2018, Zan et al.35 identified chlorogenic acid (109) from L. rotata by using high performance liquid chromatography-electrospray/quadrupole time-of-flight tandem mass spectrometry (UPLC-ESI-TOF MS). It was the first time 8-epideoxyloganic acid (110) was obtained from the ethanol extract of L. rotata by Hao Y, in 2011.43 According to published pharmacological research, both the low and high doses of 8-epideoxyloganic acid have significant analgesic and haemostatic activities, while high doses of 8-epideoxyloganic acid have anti-inflammatory properties.43 Finally, n-hexadecanoic acid (111) was isolated and identified in the 50% ethanol extract from L. rotata29,61 and fumalic acid (112) and 3,4-dimethoxycinnamic acid (113) were simultaneously identified by high-performance liquid chromatography in 2013.44

4.6 Other compounds

Additional compounds that do not fall into the categories described in the sections above that have been identified by MS, 1H-NMR, 13C-NMR, 2D-NMR and other spectral analysis techniques in L. rotata are notohamosin B (114), β-sitosterol (115), β-daucosterol (116), 3,4-dihydroxybenzaldehyde (117), and glycerol glycerin (118).34 6,7-dihydroxycoumarin (119) was identified by ESI-MS and 1H-NMR from the rhizomes of L. rotata for the first time in 2011.33 In 2015, Yin et al.30 used silica gel, macroporous resin, MCI chromatography, preparative HPLC, recrystallisation and other methods to separate compounds from L. Rotata based on their spectral data and physicochemical properties, and identified five compounds, namely, 3,4-dihydroxyphenylethanol (120), 3β-hydroxy-5α, 6α-epoxy-7-megastigmen-9-one (121), loliolide (122), isololiolide (123), and rhexifoline (124). Finally, hydroxytyrosol (125), homovanillyl alcohol (126), and 3,4-dimethoxyphenethyl alcohol (127) were simultaneously identified by high-performance liquid chromatography in L. rotata in 2013.44

5. Pharmacological activities

5.1 Anti-nociceptive activity

The analgesic activity of a purified, water-soluble L. rotata extract was studied in several pain models in rat and mice, including formalin-induced pain (phase I acute pain and phase II centrally-sensitised pain), neurogenic pain caused by spinal nerve ligation, and pain caused by bone cancer. The analgesic effects of cycloalliterpenes extracts and cycloalliterpenes monomers with different flavonoid content were investigated after formalin-induced pain in mice. Gardenioside methyl and 8-O-acetyl gardenioside methyl were administered to the spinal cord to determine the analgesic site. Oral administration of the water-soluble extract inhibited the first phase of central pain caused by formalin, as well as the hyperalgesia caused by spinal nerve ligation and bone cancer pain in rats. The analgesic effect was dose-dependent, with a maximum inhibition rate of 82%, 50% and 54%, at the median effective dose of 133.7, 236.5 and 242.9 mg kg−1, respectively. Continuous administration of the L. rotata extract for seven days did not produce analgesic tolerance in the neurogenic pain model in rats. The analgesic activity of cycloallyl ether terpene glycosides increased with its increasing concentrations within the extract, while high doses of flavonoids (1000 mg kg−1) had no analgesic effect. Therefore, in the formalin-induced pain model in mice, the content of total cycloallyl iridoid glycosides in cycloallyl ether was positively correlated with the analgesic activity through pain. Further, administration of methylgeniocide and 8-O-acetyl methylgenioside to the spinal cord inhibited formalin-induced phase II pain in rats with a dose-dependent inhibition rate of 70–80%.

There have also been studies that provide evidence for an analgesic effect of iridoid glycosides from L. rotata (IGLR) in a spared nerve injury (SNI) model. The rat SNI model was established by transversely intact peroneal and distal branches of the sciatic nerve and intact sural branches. After nerve injury, the rats were treated with different concentrations of IGLR for 14 days, whilst normal saline was administered to the negative control group. Significant mechanical abnormalities and decreased paw withdrawal mechanical threshold (PMWT) scores were observed on the first day after SNI. IGLR treatment significantly reduced SNI-induced mechanical pain, and significantly reduced the levels of nitric oxide (NO), tumour necrosis factor-a (TNF-α), interleukin-1beta (IL-1β), nitric oxide synthase (NOS), and cyclic guanosine monophosphate (cGMP), whilst increasing levels of IL-10. IGLR also inhibited N-methyl-D-aspartate receptor (NMDAR) and protein kinase C (PKCγ) protein expression, and reduced inducible NOS (iNOS) and protein kinase G type I (PKGI) mRNA levels. These results suggest that IGLR produce anti-neuropathic pain effects by partial inhibition of the NO/cGMP/PKG and NMDAR/PKC pathways and by altering the levels of cytokines in the spinal cord.45

5.2 Haemostatic activity

In traditional Chinese medicine, L. rotata has been widely been used and proven to have haemostatic effects. The aqueous extract of Herba L. rotata (HLRE) has an effect on several haemagglutination parameters, including prothrombin time (PT), thrombin time (TT), fibrinogen content (FIB) and activated partial thrombin time (APTT) when administered at different doses (high, 3 g kg−1 medium, 1.5 g kg−1 and low, 0.75 g kg−1) for a duration of 7, 14, or 21 days to rats. After seven days and 14 days of administration, TT was significantly shortened (p < 0.05) and the FIB value significantly increased (p < 0.05) at all three doses of HLRE compared with controls. After 21 days of administration, TT in the high and middle HLRE dosage groups remained shorter than TT in the control group (p < 0.05), whereas only the high dose group sustained higher FIB values compared with the controls (p < 0.05). A negative and linear correlation between TT and FIB values were observed throughout the experiment (p = 0.002). Therefore, this study showed that a dose- and time-dependent haemostatic effect is present within the aqueous extract of L. rotata and this may be mediated through shortening TTs and increasing FIB content.46

In another study, Jia et al.11 used a polyamide chromatographic column and a macroreticular resin column to purify ethanol extracts of L. rotata, and obtained flavones, total secoiridoid glycosides, and high-polarity compounds. Mice were administered with 2 g kg−1 of these purified compounds for three days before haemostatic effects were compared by a capillary coagulation test (after nicking the animals' tails). Compared with the control group that was administered physiological saline, the alcohol extract (2 g kg−1) and the secoiridoid glycoside (2 g kg−1, ig)-containing extract of L. rotata reduced the bleeding time after tail amputation by 37.4% and 49.3% respectively, and reduced the clotting time by 23.1% and 28.0%, respectively. All these fractions exhibited similar effects as the positive control drug, Yunnan Baiyao. In addition, the ethanol extract that contained iridoid glycosides in L. rotata had a haemostatic effect in mice after intra-gastric injection, leading researchers to conclude that fractions containing iridoid glycosides in L. rotata regulate blood haemostasis.

5.3 Anti-inflammatory activity

The anti-inflammatory effects of L. rotata injection (LRI) were studied in a model of granuloma formation and ear oedema in mice. To determine the anti-inflammatory activity of LRI in vitro and in vivo, the phagocytic function of macrophages was detected by phagocytosis of neutral red, and the production of IL-1 was detected by thymocyte co-stimulation. At the 0.45, 0.9, and 1.8 g kg−1 doses of LRI, dose-dependent inhibition of xylene-induced ear oedema was observed. At the 0.225 and 0.45 g kg−1 doses of LRI, protection from of cotton pellet-induced granuloma formation was 43.87–68.16% and 13.26–43.33%, respectively. Furthermore, LRI increased peritoneal macrophage phagocytosis and reduced lipopolysaccharide (LPS)-induce IL-1β production. This study showed that LRI has anti-inflammatory effects during both chronic and acute inflammation.46

The anti-inflammatory effects of L. rotata ointment have also been demonstrated in models of xylene-induced ear swelling, in acetic acid-induced abdominal capillary permeability, and during carrageenan- or adjuvant-induced foot swelling. Mice treated with 4.5, 3.0, and 1.5 g kg−1 of L. rotata ointment daily for five consecutive days had decreased capillary permeability in their abdominal cavity and reduced swelling reactions in their ears and feet, indicating marked anti-inflammatory effects of L. rotata. It is proposed that the anti-inflammatory effects are associated with inhibition of histamine synthesis and release, as well as the regulation of production of prostaglandins and other inflammatory mediators.67

The effect of L. rotata granules was investigated in a model of formaldehyde-induced persistent gingival inflammation in mice by M. Li in 2008.48 After causing inflammation, L. rotata granules were administered continuously for 5 days at three doses (high, 1.0 g kg; middle, 2.0 g kg; and low, 4.0 g kg−1), or were treated with 100 mg kg−1 of aspirin for 4 days, once a day. The daily food intake was recorded by measuring feed and cage weights, and the amount of food ingested before and after treatment was taken as an indicator of relief from gingival inflammation-induced pain. The intake of L. rotata granules in the high and middle dosage groups were higher than that in the model control group on days 4, 5 and 6 after induction of inflammation, indicating a dose-dependent effect of L. rotata granules on relieving persistent gingival inflammation.48

5.4 Anti-tumour activity

The alcohol extracts from L. rotata containing either ethereal oils, flavones, secoiridoid glycoside or high-polarity compounds were tested using an MTT (A method for detecting cell survival and growth) proliferation assay to explore the anti-tumour activities of these components. Five concentrations of the extract were prepared from an initial concentration of 25 mg mL−1 by performing dilutions in DMSO. The rate of proliferation inhibition by the different concentrations of each component was tested on SGC-7901 human gastric cancer cells, BEL-7402 liver cancer cells, and HL-60 leukaemia cells, and the corresponding hemi-inhibitory concentration (IC50) values calculated by logarithmic linear regression. The IC50 values of ethereal oil on SGC-7901, BEL-7402 and HL-60 were 78.25 μg mL−1, 113.25 μg mL−1 and 121.00 μg mL−1 respectively, which were lowest compared with IC50 values of the other components, and markedly lower than the IC50 values of total ethanol extracts. These results indicate a strong, dose-dependent inhibitory effect of ethereal oils on the proliferation of cancer cell lines in vitro, and that ethereal oil possessed more anti-tumour activity than the total ethanol extract or other components of L. rotata.11

The petroleum ether extract of L. rotata (PEELR) has also been shown to induce apoptosis in a concentration-dependent manner, which was quantified by flow cytometric detection of early apoptotic cells staining positive for annexin V and propidium iodide. The PEELR significantly inhibited the colony formation ability of the Tca8113 cell line (p < 0.05) compared with the group that did not receive treatment. The PEELR also induced increased apoptosis (p < 0.01) and decreased the ratio of Bcl-2/Bax expression (p < 0.01) compared to controls. These results indicate that the anti-tumour activity of PEELR on the Tca8113 cell line occurs as a result of reduced proliferation and increased apoptosis regulated via the Bcl-2 pathway, and this anti-tumour effect warrants further clinical investigation.49

5.5 Immunomodulatory activity

Saponin from L. rotata was injected at a dose of 50 mg kg−1 and 10 mg kg−1 into the abdominal cavity for five consecutive days to test its effect on innate immunity, specifically, on its ability to affect the number of phagocytic cells and their phagocytic rate. Saponin from L. rotata markedly improved the phagocytosis rate, phagocytic count, erythrocyte active-rosetting rate, and the rates of positive acetylase staining of macrophages, indicating an enhancement of innate immune cell activity.8

L. rotata also has an effect on the immune responses of patients infected with Mycobacterium tuberculosis. Peripheral blood mononuclear cells (PBMC) (isolated by dextran-diatrizoine density gradient centrifugation) from 20 patients with pulmonary tuberculosis and from 15 healthy controls were stimulated for 72 h, after which culture supernatants were collected to quantify γ-interferon (IFN-γ) and IL-4 levels by enzyme-linked immunosorbent assay (ELISA). The addition of L. rotata to these cultures effectively promoted the secretion of IFN-γ by PBMC from both tuberculosis patients and healthy controls (p < 0.05) but there were no differences in IL-4 levels (p > 0.05). Therefore, L. rotata could play a protective immunological role in patients infected with Mycobacterium tuberculosis by regulating the balance of Th1/Th2 cytokines.50

5.6 Other effects

In addition to the above activities, L. rotata has also cardio-protective, anti-bacterial, antioxidant, anti-fatigue, anti-gastric ulcer, and memory-boosting activities.
5.6.1 Cardio-protective effects. Doses of L. rotata in the range of 0.01–2.0 mg mL−1 were found to inhibit cardio-contractility, cardiac output, and heart rate on isolated hearts. There was a dose-dependent effect on cardio-contractility with a maximal inhibitory effect of close to 36.4%. These inhibitory effects were partially antagonised by atropine. Therefore, compounds in L. rotata may be useful for controlling cardiac excitability and angina.47
5.6.2 Anti-bacterial properties. The bacteriostatic effect of L. rotata was compared to penicillin, gentamicin, kanamycin, and chloramphenicol, by measuring bacterial growth on filter paper. L. rotata was bacteriostatic for Group B Streptococcus and Aerobacterium aerogenes, reducing the average diameter of the bacteriostasis diagram to 0.8 cm and 0.6 cm, respectively. The average diameters of L. rotata saponin-treated bacteriostatic diagrams were 1.0 cm, 0.8 cm for Pseudomonas aeruginosa, 0.7 cm for Aerobacterium, 1.0 cm for Bacillus subtilis, and 1.2 cm for Group B Streptococcus, respectively. The leaf extracts of L. rotata could also inhibit the growth of Bacillus gasoformans and Streptococcus haemolyticus. Of note, the effect of saponin from L. rotata on restraint of Bacillus gasoformans growth was significant and similar to that achieved by regular antibacterial agents.8
5.6.3 Antioxidant properties. All the regions of L. rotata with described medicinal properties contained stable and high superoxide dismutase (SOD) activity, reaching 150.87 U g−1 in some cases, providing an excellent source of H2O2-detoxifying enzymes. In addition, a higher peroxidase (POD) activity of 236.76 μmol g−1, whilst a higher efficiency of the Ascorbate–glutathione (AsA–GSH) cycle was achieved, leading to lower levels of Malondialdehyde (MDA) accumulation of 1.22 μmol g−1. These results suggest that L. rotata may enhance resistance to cellular stress due to its high-efficiency antioxidant activities.51
5.6.4 Anti-fatigue properties. Mice that received an alcohol extract of L. rotata showed extended weight-loaded swimming times under standard temperature and pressure and hypoxia, when compared with mice that received saline (p < 0.05). Their performance was better than mice that received water-soluble extracts from the herb gingko tablet, but weaker than mice that received dihydrocortisone. The alcohol extract of L. rotata also extended the lives of mice to a similar extent achieved by dihydrocortisone (p > 0.05). These results demonstrate the anti-fatigue properties of L. rotata.10
5.6.5 Oral ulcers. In oral ulcer models, induced by either acetic acid in rats or by phenol in New Zealand rabbits, oral mucosal administration of L. rotata had anti-ulcer effects. The rates of ulcer healing in rats were 44.4% and 33.3% respectively after receiving high-dose (1.5 g kg−1) and medium-dose (1.0 g kg−1) L. rotata extracts for six days, which were significantly higher than rates observed in the control group that. The L. rotata extracts resolved inflammation and reduced swelling significantly, leading to healing of ulcers – these outcomes may be related to their ability to improve blood circulation in the oral mucosa.52
5.6.6 Anti-gastric ulcer. Rats with gastric ulcer treated with ranitidine or a water-soluble extract of L. rotata exhibited different responses compared to rats treated with normal saline (p < 0.05). The L. rotata extract exerted similar effects to ranitidine, namely, by reducing the acidity and volume of gastric juices to inhibit the rate of ulcer formation (to greater than 53.3%). These results indicate that L. rotata could protect the gastric mucosa by inhibiting both gastric juice and gastric acid production.53
5.6.7 Memory-boosting functions. The effects of L. rotata and piracetam on learning and memory were studied in a model where scopolamine and ethanol were used to cause impairments in learning, memory acquisition, and recall in mice. Both doses of L. rotata extracts (0.5 g kg−1 and 1.0 g kg−1) and piracetam (0.2 g kg−1) accelerated the response time to injury upon stimulation, significantly reduced the number of errors made by the mice, and shortened their response times upon receiving an electric shock (p < 0.05 compared with the model group). The efficacy of L. rotata and piracetam were similar (p > 0.05), indicating that L. rotata could alleviate learning and memory impairment in mice.54

6. Toxicology

Despite its long history of use as a traditional Tibetan medicine, a traditional Mongolia medicine, and a traditional Chinese medicine, the potential toxicity of L. rotata has not been well addressed. L. rotata is listed for medicinal and normal consumption use, and whilst systematic evaluations of the plant's systemic toxicity and safety are lacking, no major side effects have yet been reported.

In a study where mice received 20 mL kg−1 of L. rotata extract by intravenous injection, they experienced convulsion, breathing difficulties and vomiting, and died within 1–2 minutes. However, at post mortem, no significant differences were found between the treated mice and mice that received saline (p > 0.05). The median lethal dose (LD50) was established to be 711.0 mg kg−1 (equivalent to a crude drug concentration of 4.7 g kg−1) in this study, with a confidence limit of 95% at 612.9–824.9 mg kg−1. Of mice that received 18.0 g kg−1 for 14 days, only some showed symptoms of restricted movements, fast breathing, and somnolence after an hour but they did not die. There was an average weight increase of 35.7% in these mice, but no significant pathological changes were detected upon euthanasia. As the total gavaged dose would be equivalent to 102 multiple-doses in adults, these results indicate a low level of toxicity for L. rotata.55 In a separate study, mice that received phenylethanoid glycosides from L. rotata (1.5 g kg−1 via intraperitoneal injection for 30 days) showed no damage in their hearts, lungs, thymi, testes, uterus, stomach or intestines, nor did they have abnormal appearances.56 Finally, when iridoid glycosides capsule of L. rotata was tested for toxicity, diarrhoea and less spontaneous activity were found in mice that received the 172 mg kg−1 and 430 mg kg−1 doses, in a dose-dependent manner. These adverse reactions to L. rotata capsule require further investigation.57

7. Conservation status

L. rotata is a common herb that grows in the wild that is of important medicinal and economic value in traditional Tibetan medicine and traditional Chinese medicine. In addition to being administered as a single drug, L rotata is also prepared into various formulations, including granules, capsules, tablets, dispersible tablets, soft capsules, and dripping pills. With the increase in usage of L rotata, over-exploitation has led to significant reductions on the growth of L. rotata in the wild in Gansu, Qinghai and Sichuan, such that L. rotata, is now a class II-endangered and protected plant species in Tibet.58 Lamiophlomis is the dried whole herb of L. rotata, as described in the Chinese Pharmacopoeia 2005.14 However, due to the destruction of grasslands from collectors digging for the roots of L. rotata, in recent years, the digging of entire plants has been forbidden. In order to protect the ecological environment of the alpine grassland, Lamiophlomis is the dried parts of L. rotata in the Chinese Pharmacopoeia 2015.3,59 In summary, wild resources of L. rotata have been severely degraded and whilst the ban on digging up L. rotata by the roots has been fully implemented, there are still no specific protection measures in place, and wild L. rotata resources faces significant pressure.

Therefore, there is an urgent need to establish the necessary protective measures for use and conservation of wild L. rotata. This could be achieved by strengthening the Legislation of Tibetan medicine on resource protection, and by raising awareness. Secondly, the search for alternative varieties with similar therapeutic effects could be encouraged. Finally, L. rotata could be conserved by wild tending – there is therefore an urgent need to establish a germplasm bank of Tibetan medicine to protect the germplasm resources.60–64

8. Conclusion and perspectives

Based on the analysis and evaluation of literature ranging from historical records to modern scientific publications, L. rotata, proves to be one of the most important and frequently used traditional Tibetan medicine and traditional Chinese medicine with an excellent safety record. Historically, L. rotata has been effectively used for treating traumatic injury, traumatic haemorrhage and rheumatic arthralgia; and also used to promote blood circulation, stop bleeding, dispel wind and relieve pain in clinical practice. As an ingredient, L. rotata is used in many health products including health drinks, soap, wine, mouth rinses, and biological toothpastes.65–69

Approximately 127 chemical constituents have been isolated and identified from L. rotata, including iridoids, flavonoids, phenylethanoid glycosides, polysaccharides, and organic acids. The crude extracts as well as individual compounds isolated from L. rotata show significant anti-nociceptive, haemostatic, anti-inflammatory, anti-tumour, immunomodulatory, cardio-protective, anti-bacterial, antioxidant, anti-fatigue, skin-protective, anti-gastric ulcer, and memory-boosting activities.70–72 Modern phytochemical and pharmacological studies have provided insights into some of L. rotata's mechanisms of action and demonstrated its potential for further development as an anti-tumour and anti-fatigue agent.

In conclusion, there are two important aspects to be considered in the further development and investigations of L. rotata's medicinal properties. The first is to search for chemical and biological markers from L. rotata, to guide research into its mechanisms of action, and to guide new drug discovery and quality assurance. For instance, in addition to its pharmacological and therapeutic properties, the marker compounds for quality control were changed from ‘luteolin’ to ‘shanzhiside methyl ester and 8-O-acetyl shanzhiside ethyl ester’, which were identified as major effective iridoid glycosides (IGs). IGs are pharmacologically active ingredients that can be used for quality control.24 Currently, only shanzhiside methyl ester and 8-O-acetyl shanzhiside methylester have been selected as chemical markers for evaluating the quality of L. rotata in the Chinese Pharmacopoeia 2015.3 There is therefore a need to develop more chemical and biological markers that better reflect the quality of L. rotata preparations.

The second consideration is the protection of germplasm resources and the sustainable use of L. rotata. In addition to protecting limited wild growth, L. rotata could be cultivated on a large scale on suitable mountains or plains to enable plant regeneration. Collection could also be limited to the aerial regions of the plant. The preservation of L. rotata is critical for the continued development of effective drugs targeting coagulation, hypertension, and cardiovascular disease. There is an urgent need to establish a cohesive plan for future utilisation and protection of this important medicinal resource.

Conflicts of interest

There are no conflicts to declare.

Acknowledgements

This work was financially supported by the 2018 Chinese medicine public health service subsidy special “the fourth survey on Chinese materia medica resource” (No. Finance Society [2018] 43).

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Footnote

† These authors have contributed equally to this work.
This journal is © The Royal Society of Chemistry 2020