Why the study?
Does Guben Huatan Tongmai Recipe improve lipid profiles and reduce endothelial inflammation in a rat model of high-lipid diet-induced atherosclerosis?
Does Guben Huatan Tongmai Recipe improve lipid profiles and reduce endothelial inflammation in a rat model of high-lipid diet-induced atherosclerosis?
Guben Huatan Tongmai Recipe improves lipid profiles and reduces the expression of inflammatory macrophages and cell adhesion molecules in a rat model of hyperlipidemia.
Answers are grounded in this paper and cite their sources.
Preclinical lipid and anti-inflammatory effects of GBHTTMR in rats merit human translation studies; leaves open any clinical role in atherosclerosis.
OBJECTIVE: To observe the effects of Guben Huatan Tongmai Recipe (GBHTTMR), a compound Chinese herbal recipe, on expressions of macrophages and cell adhesion molecules (CAMs) of aortic endothelia in rats with syndrome of phlegm blocking blood vessel, and to explore the pathogenesis of the phlegm-pathogen. METHODS: Fifty normal male Wistar rats, 7-week in age, were randomly divided into five groups: normal control group, untreated group, high-dose GBHTTMR-treated group, low-dose GBHTTMR-treated group and simvastatin-treated group, with 10 rats in each group. Syndrome of phlegm blocking blood vessel was induced in rats of the latter 4 groups by feeding the rats with high lipid diet. Levels of blood lipid were compared among the 5 groups. The expressions of macrophages and CAMs in aortic endothelia were tested by immunohistochemical staining method. RESULTS: The level of blood lipid, and the expressions of macrophages and CAMs showed statistical differences between the normal control group and the untreated group (P<0.01), and between the untreated group and the low-, high-dose GBHTTMR-treated and simvastatin-treated groups as well (P<0.05). CONCLUSIONS: GBHTTMR can decrease the level of serum cholesterol and triglycerides, and increase the level of high density lipoprotein. It also can inhibit the expressions of macrophages, intercellular adhesion molecule-1, vascular cell adhesion molecule-1, P-selectin, and E-selectin.
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Ping Wang (2006) studied this question.
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