Hayakawa T, Kondo T, Okumura N, Nagai K, Shibata T, Kitagawa M
Second Department of Internal Medicine, Nagoya University School of Medicine, Japan.
Am J Gastroenterol. 1989 May;84(5):523-6.
To study the effects of acarbose, an alpha-glucosidase inhibitor, on saccharide absorption and pancreatic and gut hormone release, we loaded 50 g glucose (GTT), maltose (MTT), and sucrose (STT) to 12 healthy male volunteers with and without acarbose (0, 100, or 300 mg) in a double-blind protocol. Oral load of 300 mg acarbose did not inhibit absorption of 50 g glucose; neither did it alter subsequent responses of insulin and glucagons. Maltose absorption was not influenced by acarbose up to 300 mg. However, insulin response was reduced and eteroglucagon response was enhanced by acarbose. Acarbose 100 mg markedly decreased absorption of sucrose, resulting in inhibition of plasma elevation of glucose and insulin and in enhancement of enteroglucagon release. Oral load of 30 g lactulose, nonabsorbable disaccharide, could reproduce the acarbose-induced enteroglucagon release. An increase in osmotic pressure due to retention of unabsorbed carbohydrate in the distal small intestine and proximal colon may explain the acarbose-induced enteroglucagon release and diarrhea that results from STT with acarbose.
为研究α-葡萄糖苷酶抑制剂阿卡波糖对糖类吸收以及胰腺和肠道激素释放的影响,我们采用双盲方案,让12名健康男性志愿者分别服用50克葡萄糖(葡萄糖耐量试验,GTT)、麦芽糖(麦芽糖耐量试验,MTT)和蔗糖(蔗糖耐量试验,STT),其中部分志愿者同时服用阿卡波糖(0、100或300毫克)。口服300毫克阿卡波糖并不抑制50克葡萄糖的吸收,也不改变随后胰岛素和胰高血糖素的反应。高达300毫克的阿卡波糖对麦芽糖吸收没有影响。然而,阿卡波糖会降低胰岛素反应并增强肠高血糖素反应。100毫克阿卡波糖显著降低蔗糖吸收,导致血糖和胰岛素的血浆升高受到抑制,并增强肠高血糖素释放。口服30克乳果糖(一种不可吸收的双糖)可重现阿卡波糖诱导的肠高血糖素释放。由于未吸收的碳水化合物滞留在远端小肠和近端结肠导致渗透压升高,这可能解释了阿卡波糖诱导的肠高血糖素释放以及服用阿卡波糖的蔗糖耐量试验所导致的腹泻。