1.Analysis of impact of host plants on quality of Taxilli Herba based on widely targeted metabolomics.
Dong-Lan ZHOU ; Zi-Shu CHAI ; Mei RU ; Fei-Ying HUANG ; Xie-Jun ZHANG ; Min GUO ; Yong-Hua LI
China Journal of Chinese Materia Medica 2025;50(12):3281-3290
This study aims to explore the impact of host plants on the quality of Taxilli Herba and provide a theoretical basis for the quality control of Taxilli Herba. The components of Taxilli Herba from three different host plants(Morus alba, Salix babylonica, and Cinnamomum cassia) and its 3 hosts(mulberry branch, willow branch, and cinnamon branch) were detected by widely targeted metabolomics based on ultra-high performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS). Principal component analysis(PCA), orthogonal partial least squares discriminant analysis(OPLS-DA), and Venn diagram were employed for analysis. A total of 717 metabolites were detected in Taxilli Herba from the three host plants and the branches of these host plants by UPLC-MS/MS. The results of PCA and OPLS-DA of Taxilli Herba from the three different host plants showed an obvious separation trend due to the different effects of host plants. The Venn diagram showed that there were 32, 8, and 26 characteristic metabolites in samples of Taxilli Herba from M. alba host, S. babylonica host, and C. cassia host, respectively. It was found by comparing the characteristic metabolites of Taxilli Herba and its hosts that each host transmits its characteristic components to Taxilli Herba, so that the Taxilli Herba contains the characteristic components of the host. The Kyoto Encyclopedia of Genes and Genomes(KEGG) pathway analysis showed that the differential metabolites of Taxilli Herba from the three hosts were mainly enriched in flavonoid biosynthesis, arginine and proline metabolism, and glycolysis/gluconeogenesis pathways. Furthermore, the differential metabolites enriching pathways of Taxilli Herba from the three hosts were different depending on the host. In a word, host plants have a significant impact on the metabolites of Taxilli Herba, and it may be an important factor for the quality of Taxilli Herba.
Metabolomics/methods*
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Drugs, Chinese Herbal/chemistry*
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Chromatography, High Pressure Liquid
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Tandem Mass Spectrometry
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Quality Control
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Salix/chemistry*
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Cinnamomum aromaticum/metabolism*
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Principal Component Analysis
2.Effect of guizhi decoction on PKA and PKC activities of hypothalamus in fever rats.
Jun ZHOU ; Cang-hai LI ; Hai-ru HUO ; Xu-liang KANG ; Lan-fang LI ; Nan JIANG ; Ting-lian JIANG
China Journal of Chinese Materia Medica 2006;31(1):66-69
OBJECTIVETo investigate the changes of the activity of both protein kinase A and C and the mechanisms of antipyretic action of Guizhi decoction.
METHODThe fever responses were observed after combination injection of H-89 (a selective inhibitor of PKA) and calphostin C (a selective inhibitor of PKC), and oral pretreatment of Guizhi decoction in fever rats induced by an intra-cerebroventricular (icv) injection of an EP3 agonist, and both PKA and PKC activity in hypothalamus were measured in rats pretreated with Guizhi decoction and vehicle using isotopic tracing assay.
RESULTThe rise in rat body temperature was inhibited by H-89, Calphostin C, and Guizhi decoction, moreover, pretreatment with Guizhi decoction reduced PKA activity obviously. PKC activity in model rats exhibited a tendency to drop compared with that of control group, Oral administration of Guizhi decoction in large dose inhibited the response significantly, while the low dose of Guzhi decoction has no effect on PKC.
CONCLUSIONBoth PKA and PKC may participate in the mechanism of fever induction by EP3 agonist. The decrease of PKA and PKC may contribute to the antipyretic action of Guizhi decoction, some isoenzyme of PKC may play a role in the fever production.
Analgesics, Non-Narcotic ; pharmacology ; Animals ; Cinnamomum aromaticum ; chemistry ; Cyclic AMP-Dependent Protein Kinases ; metabolism ; Dinoprostone ; analogs & derivatives ; Dose-Response Relationship, Drug ; Drug Combinations ; Drugs, Chinese Herbal ; administration & dosage ; isolation & purification ; pharmacology ; Fever ; chemically induced ; enzymology ; Hypothalamus ; enzymology ; Male ; Plants, Medicinal ; chemistry ; Protein Kinase C ; metabolism ; Random Allocation ; Rats ; Rats, Wistar ; Receptors, Prostaglandin E ; agonists ; Receptors, Prostaglandin E, EP3 Subtype
3.Adjustive effect of yi qi tong lin chongji on the three growth factors in rats prostatic tissues.
Zheng-guo MI ; Su-xiang LIU ; Yong-qing CAO ; Xiao-feng YANG
China Journal of Chinese Materia Medica 2003;28(7):653-655
OBJECTIVETo study the mechanisim of Yi Qi Tong Lin Chingji in treating benign prostatic hyperplasia.
METHODThe expressions of VEGF, bFGF and TGF beta 1 in prostatic hyperplasia model rats were examined by immunohistochemistry. 8 rats were in contrastive group, 24 influenced by Yi Qi Tong Ling Chingji and Prostacar.
RESULTThe expressions of VEGF and bFGF were significantly difference, but the expression of TGF beta 1 was not significant. (P < 0.01). The expression of VEGF and bFGF were significant in contrastive group to the high-dose of Yi Qi Tong Ling Chingji and Prostacar group (P < 0.05) but were not significant to the low-dose of Yi Qi Tong Ling Chingji group. There was no significant difference between high-dose of Yi Qi Tong Ling Chingji and Prostacar group and three growth factors.
CONCLUSIONYi Qi Tong Ling Chingji inhibit the expression of VEGF and bFGF in BPH so as to decrease the volume of prostate.
Aconitum ; chemistry ; Animals ; Cinnamomum aromaticum ; chemistry ; Diethylstilbestrol ; Drug Combinations ; Drugs, Chinese Herbal ; isolation & purification ; pharmacology ; Fibroblast Growth Factor 2 ; metabolism ; Male ; Plants, Medicinal ; chemistry ; Prostate ; metabolism ; pathology ; Prostatic Hyperplasia ; chemically induced ; metabolism ; pathology ; Rats ; Rats, Wistar ; Rehmannia ; chemistry ; Testosterone Propionate ; Transforming Growth Factor beta ; metabolism ; Transforming Growth Factor beta1 ; Vascular Endothelial Growth Factor A ; metabolism

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