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使用极小的小型猪——微型小型猪建立的无创代谢综合征模型。

Noninvasive metabolic syndrome model using an extremely small minipig, the microminipig.

作者信息

Yamaguchi Takehiro, Yamazaki Takanori, Kawaguchi Hiroaki, Tawa Masashi, Nakamura Yasuhiro, Shiota Masayuki, Osada-Oka Mayuko, Tanimoto Akihide, Okamura Tomio, Miura Katsuyuki, Iwao Hiroshi, Yoshiyama Minoru, Izumi Yasukatsu

机构信息

Department of Cardiovascular Medicine, Osaka City University Medical School, Japan.

出版信息

J Pharmacol Sci. 2014;126(2):168-71. doi: 10.1254/jphs.14171sc. Epub 2014 Sep 19.

Abstract

Metabolic syndrome (MetS) induces serious complications; therefore, we developed a noninvasive MetS model using an extremely small minipig, the Microminipig. For 8 weeks, Microminipigs were administrated a high-fat and high-cholesterol diet (HFCD) for atherosclerosis and N(G)-nitro-l-arginine methyl ester (l-NAME) for inhibiting nitric oxide synthase. HFCD significantly increased serum low-density lipoprotein levels, l-NAME increased blood pressure and cardiac hypertrophy, and HFCD-induced aortal arteriosclerosis was accelerated by l-NAME administration. Endothelium-dependent relaxation of the coronary artery was remarkably decreased by l-NAME administration. This model may be useful for elucidating the mechanisms of MetS and developing new therapeutic medicines for its treatment.

摘要

代谢综合征(MetS)会引发严重并发症;因此,我们利用一种极小的小型猪——微型小型猪,开发了一种非侵入性的MetS模型。在8周时间里,给微型小型猪喂食高脂肪高胆固醇饮食(HFCD)以诱发动脉粥样硬化,并给予N(G)-硝基-L-精氨酸甲酯(L-NAME)以抑制一氧化氮合酶。HFCD显著提高了血清低密度脂蛋白水平,L-NAME升高了血压并导致心脏肥大,而给予L-NAME加速了HFCD诱导的主动脉动脉硬化。给予L-NAME后,冠状动脉的内皮依赖性舒张功能显著降低。该模型可能有助于阐明MetS的机制,并开发治疗MetS的新治疗药物。

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