Danshen and gegen

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Actual: Danshen. 903. II. Schisandra chinensis. Wuweizi. 45. I. Scrophularia ningpoensis Gegen resulted in a dose-related suppression of acetylated-LDL uptake by.
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Background Danshen (Salviae Miltiorrhizae Radix) and Gegen (Puerariae Lobatae Radix) have been used for treating heart disease for several thousand years in China. It has been found that a Danshen and Gegen decoction (DG) exhibiting an anti-atherosclerosis effect, which improves the patients heart function recovery. Pre-treatment with DG was reported to have protective effects on myocardium

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Keywords: Chinese herbal formula; Danshen; Gegen; Stroke; Global ischaemia; Focal ischaemia. Background: Ischaemic stroke is a disease that affects many people

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Aim of the study: The present study was performed to investigate the effect of Danshen Gegen decoction on rat myocardium cell line H9c2 and the possible molecular mechanisms. Materials and methods: Rat heart myocardium H9c2 cells were treated with or without Danshen Gegen decoction (DG) ranging from 10 to 1000 ␮g/ml for 24 h.

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by X Zhou Cited by 46antagonistic, additive) between Danshen and Sanqi was analyzed using combination index (CI) and showed that the herb pair of Danshen-Gegen (

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Phenanthrenchinon ist ein Bestandteil der chinesischen Heilpflanze Danshen (Salvia miltiorrhiza). Antiphlogistikum, Antioxidanz, Zytotoxische gegen eine

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The anti-hypertensive effect of Danshen (Salvia miltiorrhiza) and Gegen (Pueraria lobata) formula in rats and its underlying mechanisms of vasorelaxation.

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The raw herbs, Danshen and Gegen, were purchased from Sichuan province and Guangdong province of China, respectively. Three aqueous extracts, Danshen alone (DE), Gegen alone (GE) as well as Danshen and Gegen in 7:3 (w/w) ratio (DGE) were prepared and authenticated by chemical markers according to our previous report (Lam et al, 2024).

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A Danshen és a Gegen (D G) általánosan használt kínai gyógynövények a szív- és érrendszeri betegségek kezelésében. A D G tanulmányt alaposan

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Danshen-Gegen formula is the leading cause for its pharmacokinetic interactions with warfarin. J Ethnopharmacol. 2024 Jul 3;154(3):

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