BMC complementary and alternative medicine · 2012
Daming capsule restores endothelial dysfunction induced by high-fat diet.
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Zhang Rong, Niu Huifang, Wang Ning, Sun Lihua, Xu Yi, Zhao Ruibo, Ban Xiang, Yu Yao, Yang Baofeng, Ai Jing
Аннотация
BACKGROUND: Daming capsule (DMC), a traditional Chinese formula, has a lipid-modulating action with reduced adverse side effects as compared with other lipid lowering compounds. Since endothelial dysfunction often accompanies the hyperlipidemic state, we hypothesize that DMC might restore endothelial dysfunction produced by a high-fat (HF) diet. Importantly, we also investigate possible mechanisms involved in mediating the effects of DMC on vascular reactivity.
METHODS: Rats were divided into four groups: control, HF diet, HF mixed DMC diet, HF mixed atorvastatin (ATV) diet. After 30 days, the thoracic cavity was exposed to remove the thoracic aorta for (i) histological examination; (ii) measurement of endothelial nitric oxide synthase (eNOS) by western blot; and (iii) tension study of thoracic aortic ring.
RESULTS: HF diet induced significant attenuation in the contraction and relaxation of rat aortic rings. Treatment with DMC significantly improved the relaxation of the aortic rings as compared with those from HF rats (P < 0.05), which was abolished by a nonspecific NOS inhibitor L-NAME. Moreover DMC significantly restored the decrease in eNOS expression induced by HF diet. Similar results were found in histopathologic changes. DMC failed to restore the loss of vasocontraction of aorta explained by an impairment of ATP-sensitive K+ channels (KATP) on the structure and/or function. DMC exerted the same protective effect as ATV, a positive control drug, on vascular injury produced by HF diet.
CONCLUSION: DMC partially protects the aorta from HF-induced endothelial dysfunction via upregulation of the expression of eNOS.
METHODS: Rats were divided into four groups: control, HF diet, HF mixed DMC diet, HF mixed atorvastatin (ATV) diet. After 30 days, the thoracic cavity was exposed to remove the thoracic aorta for (i) histological examination; (ii) measurement of endothelial nitric oxide synthase (eNOS) by western blot; and (iii) tension study of thoracic aortic ring.
RESULTS: HF diet induced significant attenuation in the contraction and relaxation of rat aortic rings. Treatment with DMC significantly improved the relaxation of the aortic rings as compared with those from HF rats (P < 0.05), which was abolished by a nonspecific NOS inhibitor L-NAME. Moreover DMC significantly restored the decrease in eNOS expression induced by HF diet. Similar results were found in histopathologic changes. DMC failed to restore the loss of vasocontraction of aorta explained by an impairment of ATP-sensitive K+ channels (KATP) on the structure and/or function. DMC exerted the same protective effect as ATV, a positive control drug, on vascular injury produced by HF diet.
CONCLUSION: DMC partially protects the aorta from HF-induced endothelial dysfunction via upregulation of the expression of eNOS.
Предметные рубрики MeSH
AnimalsAnticholesteremic AgentsAorta, ThoracicAtorvastatinDiet, High-FatDrugs, Chinese HerbalEndothelium, VascularEnzyme InhibitorsHeptanoic AcidsHyperlipidemiasHypolipidemic AgentsMaleNG-Nitroarginine Methyl EsterNitric Oxide SynthasePhytotherapyPotassium ChannelsPyrrolesRatsRats, WistarVascular DiseasesVasoconstrictionVasodilation