ABSTRACT
Different parts of Trichosanthes kirilowii can all be used as medicines, including the fruits (Trichosanthis Fructus), pericarps (Trichosanthis Pericarpium), seeds (Trichosanthis Semen) and roots (Trichosanthis Radix). Modern research has confirmed that the main active ingredients of Trichosanthis Pericarpium are flavonoids and amino acids; Trichosanthis Semen mainly contains terpenoids and sterols; Trichosanthis Radix mainly contains protein, steroids and polysaccharides. And the pharmacological effects of various medicinal parts are also different. This paper summarizes the traditional efficacy, chemical composition and modern pharmacological effects of different medicinal parts of T. kirilowii, analyzes the relationship between them, so as to analyze and predict the quality marker of T. kirilowii.
ABSTRACT
Objective: To investigate the effect of Trichosanthis Pericarpium aqueous extract(TPAE)in protecting H9c2 cells from hypoxia/reoxygenation (H/R) injury by activating phosphatidylionsitol-3-kinase/protein kinase B/nitric oxide(PI3K/Akt/NO) signaling pathway. Method: The 2.5 mmol·L-1 Na2S2O4 was used to induce the model of H9c2 cardiomyocytes H/R injury in the experiments. The cultured H9c2 cardiomyocytes were randomly divided into normal group, H/R group (model group) and inhibition group (LY294002, 10 μmol·L-1). In the H/R + TPAE group, 50 mg·L-1 TPAE was added to the cultures at 24 h before H/R exposure. Cell viability was measured by methyl thiazolyl tetrazolium (MTT) assay. The amounts of NO, endothelial nitric oxide synthase (eNOS), and induced nitric oxide synthase (iNOS) were tested by enzyme linked immunosorbent assay (ELISA) kits. Reverse transcription-quantitative real-time polymerase chain reaction (Real-time PCR) was performed to analyze relative mRNA expressions of Akt, eNOS and iNOS. Western blot was used to detect the expressions of Akt, p-Akt (Ser 473), eNOS, and iNOS. Result: Compared with the normal control group,the cell viability significantly decreased in the model control group (PPPPPPPPConclusion: TPAE can protect H9c2 cardiomyocytes from H/R injury by activating PI3K/Akt signaling pathway,which might be related to the up-regulation of the mRNA and protein expressions of eNOS, the down-regulation of the level of iNOS, and the increase of the production of physiological amounts of NO.
ABSTRACT
To isolate the anti-angiotensin converting enzyme (ACE) constituents from Trichosanthis Pericarpium based on bioactivity-guided separation. Trichosanthis Pericarpium was extracted with boiling water and precipitated by ethanol, then its supernatant was collected and dialyzed. The retentate of the fractions above 1 000 was lyophilized to obtain GLP, which was then successively separated by DEAE Sepharose fast flow anion-exchange and Superdex-75 gel permeation chromatographic steps to achieve GLP-1-1. A combination of HPGPC, monosaccharide compositions determination and ACE inhibitory activity studies was performed to investigate the structure and bioactivity. The results showed that an anti-angiotensin converting enzyme oligosaccharide, GLP-1-1, was obtained from Trichosanthis Pericarpium based on activity tracking, whose average molecular weight was estimated to 1 367; mainly composed of arabinose, mannose, and glucose at a ratio of 0.2∶4.3∶10.0. GLP-1-1 showed potent anti-angiotensin converting enzyme effect with the IC₅₀of (113.4±8.6) mg•L⁻¹. In this study, an oligosaccharide with anti-angiotensin converting enzyme effect was isolated from Trichosanthis Pericarpium, which could lay the foundation for the substance basis study of Trichosanthis Pericarpium.
ABSTRACT
Objective To isolate anti-renin constituents from Trichosanthis Pericarpium based on bioactivity tracking separation. Methods T. Pericarpium was extracted with boiling water and precipitated by ethanol, the supernate was collected and dialyzed, and the retentate was lyophilized giving GLP, then successively separated by DEAE Sepharose Fast Flow anion-exchange and Superdex-75 gel permeation chromatographic steps, to give GLP-5-1. A combination of HPGPC, monosaccharide composition, and anti-renin studies was performed to investigate the structure and bioactivity. Results An anti-renin polysaccharide, GLP-5-1, was obtained from T. Pericarpium based on activity tracking, the average molecular weight was estimated to 3 722, monosaccharide composition analysis showed GLP-5-1 contained arabinose, mannose, glucose, and galactose with the ratio of 5.5:4.4:6.9:10.0. GLP-5-1 showed potent anti-renin effect with the IC50 was (87.4 ± 6.8) μg/mL. Conclusion In this study, a low molecular weight polysaccharide with anti-renin effect was isolated from T. Pericarpium, which could lay the foundation for the substance basis study of T. Pericarpium.
ABSTRACT
Objective: To analyze the quality of medicinal parts of Trichosanthes kirilowii from different populations and to establish a new method to evaluate the medicinal material quality. Methods: Contents of protein, flavonoids, and polysaccharide were analyzed by AA3 Continuous Flow, ultraviolet-visible spectrophotometry, and sulfuric acid-phenol. The 3, 29-dibenzoyl rarounitriol (3, 29-DR) content in Trichosanthis Semen and the cucurbitacin bcontent in Trichosanthis Radix were determined by RP-HPLC. In addition, the quality of medicinal materials was evaluated by the principal components analysis (PCA) and cluster analysis. Results: The quality of Trichosanthis Semen was the best in T. kirilowii from Henan Anyang-Liyuan with highest contents of 3, 29-DR and protein; Shanxi Jiang County T. kirilowii can be better used as Trichosanthis Pericarpium with higher contents of protein and polysaccharide; T. kirilowii from Anhui Yuexi-Heidapian could be regarded as Trichosanthis Radix for cultivating, because of higher protein content, lower starch content, and medium cucurbitacin bcontent. Conclusion: The PCA and cluster analysis are effective in evaluating the medicinal material quality. The newly established model will bring the significant benefits for evaluating the quality of T. kirilowii.