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Background: Lysimachia christinae Hance (LCH) is a traditional medicine used to treat gallstone disease and cholecystitis. Despite its known anti-inflammatory and choleretic effects, its quality has not been extensively evaluated., Objective: In this study, we aimed to establish a reliable quality evaluation method for LCH via fingerprint, spectrum-effect relationship, and quantitative analyses of multicomponents by a single marker (QAMS)., Methods: First, the fingerprints and anti-inflammatory and choleretic activities of 14 LCH batches were determined. Then, the gray relation analysis method was used to analyze the peak areas of the fingerprint profile and pharmacodynamic data. Subsequently, the characteristic peaks were tentatively identified using high-performance liquid chromatography-quadrupole time-of-flight mass spectrometry. Finally, rutin was selected as the internal reference material, and QAMS was used to analyze the LCH components., Results: Pharmacodynamic experiments confirmed that LCH exerted anti-inflammatory and choleretic effects. Moreover, 15 flavonoids related to the anti-inflammatory and choleretic effects of LCH were identified. Notably, relative error percentage between the QAMS and external standard method was less than 5%., Conclusion: This study successfully established a comprehensive evaluation method for the qualitative and quantitative analyses of LCH., (© 2024 John Wiley & Sons Ltd.)

Phytochemical investigation on aerial parts of Lysimachia atropurpurea L. (Myrsinaceae), guided by NMR methods, resulted in the isolation and characterization of three previously undescribed triterpenoid saponins named stralysaponins A-C along with five known compounds. Their structures were elucidated by 1D and 2D NMR spectroscopy and HR-ESI-MS. Stralysaponins A-C were categorized into 13β-28-epoxyoleanane-type triterpenoid saponins, reaffirming their prevalent presence of this type in the Myrsinaceae family and the genus Lysimachia. The identified derivatives share a common four-unit branched sugar chain, with rhamnose as the terminal sugar linked at C-3 of the aglycone. The presence of triterpenoid saponins in L. atropurpurea is reported herein for the first time. This study enriched the chemical diversity of triterpenoid saponins of the genus Lysimachia. Additionally, it demonstrates the effectiveness of NMR-profiling in isolating previously undescribed triterpenoid saponins from Lysimachia spp., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 Elsevier Ltd. All rights reserved.)

A novel acidic heteropolysaccharide (LCP-90-1) was isolated and purified from a traditional "heat-clearing" Chinese medicine, Lysimachia christinae Hance. LCP-90-1 ( Mw , 20.65 kDa) was composed of Man, Rha, GlcA, Glc, Gal, and Ara, with relative molar ratios of 1.00: 3.00: 11.62: 1.31: 1.64: 5.24. The backbone consisted of 1,4- α -D-Glc p A, 1,4- α -D-Glc p , 1,4- β -L-Rha p , and 1,3,5- α -L-Ara f , with three branches of β -D-Gal p -(1 → 4)- β -L-Rha p -(1→, α -L-Ara f -(1→ and α -D-Man p -(1→ attached to the C-5 position of 1,3,5- α -L-Ara f . LCP-90-1 exhibited potent anticomplement activity (CH 50 : 135.01 ± 0.68 µg/mL) in vitro , which was significantly enhanced with increased glucuronic acid (GlcA) content in its degradation production (LCP-90-1-A, CH 50 : 28.26 ± 0.39 µg/mL). However, both LCP-90-1 and LCP90-1-A were inactivated after reduction or complete acid hydrolysis. These observations indicated the important role of GlcA in LCP-90-1 and associated derivatives with respect to anticomplement activity. Similarly, compared with LCP-90-1, the antioxidant activity of LCP-90-1-A was also enhanced. Thus, polysaccharides with a high content of GlcA might be important and effective substances of L. christinae ., Competing Interests: The authors declare that they have no conflict of interest., (Thieme. All rights reserved.)

Genetic divergence between species depends on reproductive isolation (RI) due to traits that reduce interspecific mating (prezygotic isolation) or are due to reduced hybrid fitness (postzygotic isolation). Previous research found that prezygotic barriers tend to be stronger than postzygotic barriers, but most studies are based on the evaluation of F 1 hybrid fitness in early life cycle stages. We combined field and experimental data to determine the strength of 17 prezygotic and postzygotic reproductive barriers between two Lysimachia species that often co-occur and share pollinators. We assessed postzygotic barriers up to F 2 hybrids and backcrosses. The two species showed near complete RI due to the cumulative effect of multiple barriers, with an uneven and asymmetric contribution to isolation. In allopatry, prezygotic barriers contributed more to reduce gene flow than postzygotic barriers, but their contributions were more similar in sympatry. The strength of postzygotic RI was up to three times lower for F 1 progeny than for F 2 or backcrossed progenies, and RI was only complete when late F 1 stages and either F 2 or backcrosses were accounted for. Our results thus suggest that the relative strength of postzygotic RI may be underestimated when its effects on late stages of the life cycle are disregarded., (© 2023 The Authors. New Phytologist © 2023 New Phytologist Foundation.)

Abstract Background Lysimachia L., the second largest genus within the subfamily Myrsinoideae of Primulaceae, comprises approximately 250 species worldwide. China is the species diversity center of Lysimachia, containing approximately 150 species. Despite advances in the backbone phylogeny of Lysimachia, species-level relationships remain poorly understood due to limited genomic information. This study analyzed 50 complete plastomes for 46 Lysimachia species. We aimed to identify the plastome structure features and hypervariable loci of Lysimachia. Additionally, the phylogenetic relationships and phylogenetic conflict signals in Lysimachia were examined. Results These fifty plastomes within Lysimachia had the typical quadripartite structure, with lengths varying from 152,691 to 155,784 bp. Plastome size was positively correlated with IR and intron length. Thirteen highly variable regions in Lysimachia plastomes were identified. Additionally, ndhB, petB and ycf2 were found to be under positive selection. Plastid ML trees and species tree strongly supported that L. maritima as sister to subg. Palladia + subg. Lysimachia (Christinae clade), while the nrDNA ML tree clearly placed L. maritima and subg. Palladia as a sister group. Conclusions The structures of these plastomes of Lysimachia were generally conserved, but potential plastid markers and signatures of positive selection were detected. These genomic data provided new insights into the interspecific relationships of Lysimachia, including the cytonuclear discordance of the position of L. maritima, which may be the result of ghost introgression in the past. Our findings have established a basis for further exploration of the taxonomy, phylogeny and evolutionary history within Lysimachia.

Lysimachia foenum-graecum Hance (Primulaceae) is a medicinal plant used for cold, pain, ascariasis, etc., in China. Triterpenoid saponins have been found to be the main components of this genus. In this work, a pair of oleanane-type triterpenoid saponins with an unprecedented 4/5/6 fused tricyclic skeleton, foegraecumoside O (1) and foegraecumoside P (2) were isolated from the butanol fraction of the aerial parts of L. foenum-graecum. Their structures were determined using chemical methods and extensive spectroscopic analyses, along with quantum chemical calculations. Compound 2 displayed moderate cytotoxicity against HepG2, MGC-803, T24, NCI-H460, A549, and A549/CDDP (drug-resistant lung-cancer cell line) with IC50 at 12.4–19.2 μM in an MTT assay, comparing with the positive control doxorubicin, which had IC50 at 0.53–4.92 μM, but was inactive for A549/CDDP. Furthermore, a possible biosynthetic pathway for forming compounds 1 and 2 was proposed.

Lysimachia danxiashanensis, a new Primulaceae species, endemic to the Danxia landscape in Guangdong Province, China, is described and illustrated. This new species is morphologically similar to L. pseudohenryi, L. phyllocephala, L. congestiflora and L. kwangtungensis, but it differs from the similar species by its purplish-red plants, petiole without wings, calyx with orange glandular and the corolla margin serrated on upper half with orange-red glandular punctates. This new species belongs to Lysimachia subgen. Lysimachia sect. Nummularia. Phylogenetic analysis confirmed that L. danxiashanensis is a distinct clade, based on the combined data of ITS and rbcL sequences. The conservation status of the new species was evaluated as Endangered (EN) according to IUCN Red List Categories and Criteria. [ABSTRACT FROM AUTHOR]

Several species of the genus Lysimachia L. (Primulaceae) are well known in folk medicine, but very few studies have been conducted on them. The aim of our study was to investigate the microscopical characteristics and chemical composition of Lysimachia insignis Hemsl., L. decurrens G. Forst., and L. congestiflora Hemsl. as well as to evaluate some biological activities of their methanol extracts. The transverse sections of stem and powder characteristics of the three Lysimachia species shared some similarities. Also, some differences were indicated. The chemical investigation of three aforesaid species including the preliminary phytochemical screening, the quantification of the total polyphenol content and total flavonoid content, as well as the determination of metabolites. The phytochemical screening showed the presence of flavonoids, saponins, tannins and sterols in all the three species. On the other hand, coumarins were detected in L. insignis while anthranoids were present in L. decurrens and L. congestiflora. The total polyphenol content and the total flavonoid content of the aforesaid species were determined by the spectrometric method. The metabolite profiling approach of three species was performed by LC-Q-ToF-HRMS and HPTLC. The methanol extract of L. insignis showed a weak inhibitory effect on NO production (I% = 57.4 at the concentration of 100 µg/ml) while the extract of L. decurrens exhibited moderate anti-oxidant activity in vitro (SC% = 62.5 at the concentration of 100 µg/mL).

In this study, the wound healing potential of L. verticillaris and L. vulgaris were investigated in vivo with the "Circular Excision Wound Model". Changes in wound healing have been observed with biological activity and histopathological studies. RT-PCR studies were performed to determine gene expression. Moreover, enzyme inhibitions, antimicrobial activity and HPLC studies were carried out. When the wound area closures were examined, it was determined that the wound closure effect of the ointments was better than the Madecassol®. It was observed that the species contributed to wound healing by decreasing TNF-α, IL-1β and MMP-9 gene levels and increasing IL-10 levels. The collagenase enzyme inhibition values of the species were found to be close to each other and as effective as catechin. It was determined that the species showed the most pronounced antimicrobial activity against S. aureus. Sinapic acid was detected as the major compound in HPLC studies. [Display omitted] • The wound healing potential of the groups that applied ointment containing 5 % extracts were found to be more effective. • It was observed that antioxidant and anti-inflammatory effects were best in groups containing 5 % ointment. • The extracts were reduced the mRNA expression of TNF-α, IL-1β and MMP-9. • Collagenase enzyme inhibition of the extracts was found to be as effective as catechin. • In HPLC studies, sinapic acid was determined as the main component. [ABSTRACT FROM AUTHOR]

Lysimachia nummularia L. is a plant belonging to the Primulaceae family, which is particularly valuable as a medicinal raw material used in folk medicine in many countries. It has excellent antibacterial and antioxidant capacity of metabolites. That is why the microclonal propagation of Lysimachia nummularia L. is a relevant issue. The purpose of this paper is to develop approaches to microclonal propagation of L. nummularia. For microclonal reproduction of L. nummularia, the method of activation of isolated tissues and organs already present in the plant meristem and induction of direct regeneration directly by explant tissues was used. To select highly productive cell lines of representatives of the genus Lysimachia, callus culture was obtained by indirect morphogenesis from stem and leaf explants. It was found that the formation of tissues and organs of L. nummularia into in vitro culture depended on the composition of the nutrient medium and the quantitative and qualitative ratio of growth regulators in it. Active proliferation of L. nummularia microshoots into in vitro culture was noted on the variants of Murashige and Skoog, and Driver and Kuniyuki nutrient medium with 6-benzylaminopurine 4.0 mg∙l -1, indolyl butyric acid 0.03 mg∙l -1, gibberellic acid 0.1 mg∙l -1. It was established that for microclonal reproduction, induction, and proliferation of the root system and obtaining regenerating plants of L. nummularia, the most effective is the use of nutrient media according to Murashige and Skoog with the addition of thidiazuron 0.5 mg∙l -1 and 0.25 mg∙l -1 kinetin. The optimal conditions for the induction of callusogenesis and obtaining the culture of cells and callus tissues of L. nummularia and its passage in vitro were selected. It has been shown that the modified nutrient medium of Murashige and Skoog, with 2.4-dichlorophenacetic acid 1.5 mg∙l -1 and indole-3-acetic acid 0.2 mg∙l -1, is optimal for the accumulation of callus tissue biomass of L. nummularia, which ensured the frequency of callusogenesis for the first and second passages up to 98.0 ± 0.2%. 5 cell lines that actively synthesize stilbenoids and the highly productive LN-EE 02/19 cell line, which is capable of synthesizing and accumulating in callus tissues up to 10-12 mg∙g-1 of myricetrin, were selectively isolated. As a result of the analysis, the callus culture cell line LN-EE 02/19 was obtained, which allows obtaining myricetrin in amounts up to 10.0-12.0 mg∙l -1 of raw biomass. The developed protocol can be used both for L. nummularia plants and other representatives of the Primulaceae family. [ABSTRACT FROM AUTHOR]

Lysimachia nummularia L. is a perennial herbaceous plant rich in bioactive compounds, which can be utilized for medicinal purposes. The present work aims to analyze the phenolic compounds from different parts of the Lysimachia nummularia L. plant using the HPLC technique: Lysimachiae radix (the root part), Lysimachiae herba (the aerial part), Lysimachiae flores (flowers). In order to determine the phenolic compounds, extraction from the three categories of vegetable products was performed with ethanol 70% (v/v) using three extraction methods: (i) Soxhlet extraction, (ii) maceration and (iii) ultrasonic-assisted extraction. The content of polyphenols was determined by the Folin–Ciocalteu method, and the antioxidant activity was evaluated by the DPPH, ABTS, FRAP and CUPRAC methods. The antioxidant activity was correlated with the content of phenolic compounds in the analyzed extracts. The following phenolic compounds were separated, identified and quantified: 3-O-methylgallic, gallic, ferulic, caffeic, chlorogenic, p-coumaric acids and trans-resveratrol. According to the experimental data, the highest content of total polyphenols was observed in the hydroethanolic extract from Lysimachiae flores (22.10 ± 1.48 mg gallic acid/g), which also presented remarkable antioxidant activity.

Lysimachia christinae Hance is widely distributed in subtropical China at the elevational range from 500–2300 m. The species is an important medicinal herb for treating jaundice, urinary disorders, and the liver. Here, we sequenced and characterized the whole plastid genome of L. christinae. It is 154,810 bp in length, containing two copies of inverted repeat (IR) regions (26,034 bp, each), a large single-copy (LSC) region (84,809 bp), and a small single-copy (SSC) region (17,933 bp). It has 114 genes, of which 80 are protein-coding, 30 are tRNA, and 4 are rRNA genes. The ML tree indicates L. christinae is closely related to Lysimachia congestiflora Hemsl. This genome information can help us better construct a backbone phylogeny of Lysimachia in the future.

Lysimachia foenum-graecum Hance (Primulaceae) is a medicinal plant used for cold, pain, ascariasis, etc., in China. Triterpenoid saponins have been found to be the main components of this genus. In this work, a pair of oleanane-type triterpenoid saponins with an unprecedented 4/5/6 fused tricyclic skeleton, foegraecumoside O (1) and foegraecumoside P (2) were isolated from the butanol fraction of the aerial parts of L. foenum-graecum. Their structures were determined using chemical methods and extensive spectroscopic analyses, along with quantum chemical calculations. Compound 2 displayed moderate cytotoxicity against HepG2, MGC-803, T24, NCI-H460, A549, and A549/CDDP (drug-resistant lung-cancer cell line) with IC50 at 12.4–19.2 μM in an MTT assay, comparing with the positive control doxorubicin, which had IC50 at 0.53–4.92 μM, but was inactive for A549/CDDP. Furthermore, a possible biosynthetic pathway for forming compounds 1 and 2 was proposed. [ABSTRACT FROM AUTHOR]

This study aimed to determine the type of seed dormancy and to identify a suitable method of dormancy-breaking for an efficient seed viability test of Lysimachia coreana Nakai. To confirm the effect of gibberellic acid (GA3) on seed germination at different temperatures, germination tests were conducted at 5, 15, 20, 25, 20/10, and 25/15 °C (12/12 h, light/dark), using 1% agar with 100, 250, and 500 mg·L−1 GA3. Seeds were also stratified at 5 and 25/15 °C for 6 and 9 weeks, respectively, and then germinated at the same temperature. Seeds treated with GA3 demonstrated an increased germination rate (GR) at all temperatures except 5 °C. The highest GR was 82.0% at 25/15 °C and 250 mg·L−1 GA3 (4.8 times higher than the control (14.0%)). Additionally, GR increased after cold stratification, whereas seeds did not germinate after warm stratification at all temperatures. After cold stratification, the highest GR was 56.0% at 25/15 °C, which was lower than the GR observed after GA3 treatment. We hypothesized that L. coreana seeds have a non-deep physiological dormancy and concluded that 250 mg·L−1 GA3 treatment is more effective than cold stratification (9 weeks) for L. coreana seed-dormancy-breaking.

A new species, Lysimachia coriacea, from Chongqing, China, is described and illustrated. It is assigned to subgen. Lysimachia sect. Nummularia ser. Paridiformes and resembles L. paridiformis var. stenophylla, but is characterised by smaller leathery leaves with black glandular striations near the margin. It is also similar to L. nanpingensis in its two to three pairs of leaves sub-whorled at the stem apices, but differs by smaller leathery leaves and densely glandular stem, petiole and pedicel, and calyx lobes with sparse black glandular stripes. [ABSTRACT FROM AUTHOR]

A new species, Lysimachia septemfida (Primulaceae), from Yunnan (Southwest China) is described and illustrated. The new species exhibits several unusual characters in Lysimachia including lack of a corolla, 7-merous flowers, leaves in whorls of 3 and distinct multicellular nodiferous hairs, which make it readily distinguishable from all other species in this genus. The diagnostic differences between this new species and its suppositive allies are given. In addition, the systematic placement of this new species is also discussed based on an ITS molecular tree.

A new species of Lysimachia (Primulaceae), Lysimachia tianmaensis K. Liu, S.B. Zhou & Ying Wang sp. nov., is described and illustrated from Jinzhai County, Anhui, China. It is endemic to Dabieshan Mountain, China. The new species has yellow flowers and belongs to the subgenus Lysimachia section Nummularia series Grammicae. It is very easily distinguishable from other related species by having alternate leaves with brown patches beneath and an auriculated leaf base. [ABSTRACT FROM AUTHOR]

Six previously undescribed oleanane-type triterpenoid saponins, fortunosides A–F, together with six known ones, were isolated from the aerial parts of L ysimachia fortunei Maxim. Their structures were established by spectroscopic data analyses (1D, 2D-NMR and HRESIMS) and chemical methods. All isolated triterpenoid saponins were evaluated for their cytotoxicity against four human liver cancer cell lines (SMMC-7721, Hep3B, HuH7, and SK-Hep-1). Three saponins with the aglycone protoprimulagenin A exhibited moderate cytotoxicity against all of the tested human cancer cell lines, with IC 50 values ranging from 4.76 to 15.12 μM. [ABSTRACT FROM AUTHOR]

Varicella‑zoster virus (VZV), a ubiquitous human α‑herpesvirus, is the causative agent of chickenpox and shingles. In the present study, we investigated the antiviral activity of a 70% ethanol extract of Lysimachia mauritiana (LME) against VZV. LME strongly interfered with the replication of both laboratory and clinical strains of VZV without affecting the viability of MRC‑5 cells. Moreover, LME treatment suppressed the expression of an essential viral transactivator, immediate‑early 62 protein (IE62), in addition to other lytic genes in the later phases of viral replication. The finding that LME exerts potent inhibitory effects on VZV gene expression and replication supports its potential utility as a therapeutic anti‑viral agent. [ABSTRACT FROM AUTHOR]

Foenumoside B (FSB), a bioactive component isolated from the Lysimachia foenum-graecum extract (LFE), has been shown to possess anti-inflammatory effects, but the underlying molecular mechanisms involved have not been elucidated. Accordingly, the authors investigated the mechanisms responsible for the anti-inflammatory effects of FSB in murine macrophages activated by LPS. FSB suppressed the LPS-induced expressions of iNOS and COX-2 at protein and mRNA levels and consequently decreased NO and PGE2 production in RAW264.7 and primary macrophages. FSB also reduced the LPS-induced inductions of TNF-α, IL-6 and IL-1β at protein and mRNA levels. Studies of the molecular mechanisms involved in the anti-inflammatory effects of FSB showed that it inhibited the transcriptional activities of NF-κB and AP-1, and the nuclear translocation of NF-κB via inhibition of the phosphorylations of AKT, p38 and STAT3. In a sepsis model, pretreatment with FSB inhibited the LPS-stimulated mRNA and protein levels of proinflammatory mediators, such as, iNOS, COX-2, TNF-α, IL-6 and IL-1β in plasma and liver. Importantly, FSB increased the survival rate of mice in the LPS-induced sepsis model. Taken together, these results show that the anti-inflammatory effects of FSB against LPS-induced inflammatory conditions are associated with inhibitions of the phosphorylations of AKT, p38 and STAT3 followed by the transcriptional suppressions of NF-κB and AP-1, and thus, reduced expressions of pro-inflammatory genes. [ABSTRACT FROM AUTHOR]