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阿卡波糖,一种α-葡萄糖苷酶抑制剂,可改善喂食果糖的大鼠的胰岛素抵抗。

Acarbose, an alpha-glucosidase inhibitor, improves insulin resistance in fructose-fed rats.

作者信息

Nakamura K, Yamagishi S, Matsui T, Inoue H

机构信息

Department of Medicine, Kurume University School of Medicine, Kurume, Japan.

出版信息

Drugs Exp Clin Res. 2005;31(4):155-9.

PMID:16223205
Abstract

Insulin resistance is one of the determinants of postprandial hyperglycemia. Acarbose is an alpha-glucosidase inhibitor that delays the absorption of carbohydrates from the small intestine, thereby suppressing postprandial hyperglycemia. Recently, acarbose has been found to reduce the incidence of cardiovascular disease (CVD) in patients with diabetes. These observations suggest that intervention of postprandial hyperglycemia with acarbose is a promising strategy for the prevention of CVD in diabetic patients. However, the effects of acarbose on insulin sensitivity are not fully understood. In this study, we examined whether oral administration of acarbose could improve insulin sensitivity in fructose-fed rats, a widely used insulin-resistant animal model. Although plasma glucose levels remained unchanged during the experiments, serum insulin levels were significantly increased in fructose-fed rats, which were suppressed by 4 weeks of treatment with acarbose. Acarbose treatment also increased high-density lipoprotein levels in fructose-fed rats. Furthermore, treatment of acarbose inhibited the elevation of systolic blood pressure levels in fructose-fed rats. These results indicate that oral administration of acarbose improves insulin sensitivity in fructose-fed rats. Our present study suggests that the cardioprotecive effects of acarbose could be ascribed, at least in part, to its insulin-sensitizing property.

摘要

胰岛素抵抗是餐后高血糖的决定因素之一。阿卡波糖是一种α-葡萄糖苷酶抑制剂,可延迟碳水化合物从小肠的吸收,从而抑制餐后高血糖。最近,已发现阿卡波糖可降低糖尿病患者心血管疾病(CVD)的发生率。这些观察结果表明,用阿卡波糖干预餐后高血糖是预防糖尿病患者CVD的一种有前景的策略。然而,阿卡波糖对胰岛素敏感性的影响尚未完全了解。在本研究中,我们研究了口服阿卡波糖是否能改善用果糖喂养的大鼠(一种广泛使用的胰岛素抵抗动物模型)的胰岛素敏感性。尽管在实验过程中血浆葡萄糖水平保持不变,但果糖喂养的大鼠血清胰岛素水平显著升高,用阿卡波糖治疗4周可使其受到抑制。阿卡波糖治疗还可提高果糖喂养大鼠的高密度脂蛋白水平。此外,阿卡波糖治疗可抑制果糖喂养大鼠收缩压水平的升高。这些结果表明,口服阿卡波糖可改善果糖喂养大鼠的胰岛素敏感性。我们目前的研究表明,阿卡波糖的心脏保护作用至少部分可归因于其胰岛素增敏特性。

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1
Acarbose, an alpha-glucosidase inhibitor, improves insulin resistance in fructose-fed rats.阿卡波糖,一种α-葡萄糖苷酶抑制剂,可改善喂食果糖的大鼠的胰岛素抵抗。
Drugs Exp Clin Res. 2005;31(4):155-9.
2
Inhibition of postprandial hyperglycemia by acarbose is a promising therapeutic strategy for the treatment of patients with the metabolic syndrome.阿卡波糖抑制餐后高血糖是治疗代谢综合征患者的一种有前景的治疗策略。
Med Hypotheses. 2005;65(1):152-4. doi: 10.1016/j.mehy.2004.12.008. Epub 2005 Jan 28.
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Acarbose reduces blood pressure in sucrose-induced hypertension in rats.阿卡波糖可降低蔗糖诱导的大鼠高血压模型的血压。
Isr J Med Sci. 1997 Mar;33(3):153-9.
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Acarbose is a promising therapeutic strategy for the treatment of patients with nonalcoholic steatohepatitis (NASH).阿卡波糖是治疗非酒精性脂肪性肝炎(NASH)患者的一种有前景的治疗策略。
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Effect of inhibition of alpha-glucosidase on age-related glucose intolerance and pancreatic atrophy in rats.α-葡萄糖苷酶抑制对大鼠年龄相关性葡萄糖不耐受和胰腺萎缩的影响。
Metabolism. 2006 Apr;55(4):533-40. doi: 10.1016/j.metabol.2005.11.007.
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Acarbose, an alpha-glucosidase inhibitor, decreases aortic gene expression and serum levels of monocyte chemoattractant protein-1 in fructose-fed rats.
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Postprandial serum lipids and tissue lipoprotein lipase are acutely altered in rats by the alpha-glucosidase inhibitor acarbose.α-葡萄糖苷酶抑制剂阿卡波糖可使大鼠餐后血清脂质和组织脂蛋白脂肪酶发生急性改变。
Horm Metab Res. 1996 Aug;28(8):377-80. doi: 10.1055/s-2007-979819.
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Effects of the alpha-glucosidase inhibitor acarbose on postprandial serum glucose and insulin concentrations in healthy dogs.α-葡萄糖苷酶抑制剂阿卡波糖对健康犬餐后血清葡萄糖和胰岛素浓度的影响。
Am J Vet Res. 1999 May;60(5):541-5.
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Acarbose, an alpha-glucosidase inhibitor, improves endothelial dysfunction in Goto-Kakizaki rats exhibiting repetitive blood glucose fluctuation.阿卡波糖,一种α-葡萄糖苷酶抑制剂,可改善表现出反复血糖波动的Goto-Kakizaki大鼠的内皮功能障碍。
Biochem Biophys Res Commun. 2006 Jun 30;345(2):688-93. doi: 10.1016/j.bbrc.2006.04.090. Epub 2006 May 2.
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Long-term effect of alpha-glucosidase inhibitor on late dumping syndrome.α-葡萄糖苷酶抑制剂对晚期倾倒综合征的长期影响。
J Gastroenterol Hepatol. 1998 Dec;13(12):1201-6.

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