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人胃肠道中3-羟基-3-甲基戊二酰辅酶A还原酶的活性

3-Hydroxy-3-methylglutaryl coenzyme A reductase activity in the human gastrointestinal tract.

作者信息

Gebhard R L, Stone B G, Prigge W F

出版信息

J Lipid Res. 1985 Jan;26(1):47-53.

PMID:3973513
Abstract

Activity of 3-hydroxy-3-methylglutaryl coenzyme A reductase (EC 1.1.1.34) was measured in intestinal mucosa of the human gastrointestinal tract. Activity was highest in gastric mucosa (18.2 pmol per mg per min) and there was a constant low level in the small bowel and colon (approximately 10 pmol per mg per min). Phosphorylation/dephosphorylation modulation of intestinal reductase activity was demonstrated in normal mucosa. Expressed jejunal reductase activity was significantly higher in celiac sprue mucosa and mucosa from defunctionalized intestine of jejunoileal bypass patients. Enzyme activity also increased during 24-hr mucosal organ culture in the absence of exogenous cholesterol. Addition to the culture medium of pure cholesterol or 25-hydroxycholesterol dissolved in a small volume of ethanol suppressed the culture-induced increase to 86 +/- 3% and 69 +/- 5% of paired controls, respectively. This evidence suggests that a moderate degree of feedback regulation of intestinal cholesterol synthesis by luminal sterol occurs in man. Mucosal HMG-CoA reductase activity was also measured in patients with hyperlipoproteinemia. Patients with either predominant hypercholesterolemia or predominant hypertriglyceridemia lipid profiles had "normal" expressed reductase activity, but feedback regulation by free cholesterol could not be demonstrated in either group under these conditions.

摘要

在人类胃肠道的肠黏膜中测定了3-羟基-3-甲基戊二酰辅酶A还原酶(EC 1.1.1.34)的活性。胃黏膜中的活性最高(每分钟每毫克18.2皮摩尔),而小肠和结肠中的活性处于恒定的低水平(约每分钟每毫克10皮摩尔)。在正常黏膜中证实了肠道还原酶活性的磷酸化/去磷酸化调节。乳糜泻黏膜和空肠回肠旁路患者去功能化肠道的黏膜中,空肠还原酶的表达活性显著更高。在没有外源性胆固醇的情况下,在24小时黏膜器官培养期间酶活性也会增加。向培养基中添加溶解于少量乙醇中的纯胆固醇或25-羟胆固醇,分别将培养诱导的增加抑制至配对对照的86±3%和69±5%。这一证据表明,人体肠道胆固醇合成存在一定程度的腔内固醇反馈调节。还对高脂蛋白血症患者的黏膜HMG-CoA还原酶活性进行了测定。以高胆固醇血症为主或高甘油三酯血症为主的脂质谱患者,其还原酶的表达活性“正常”,但在这些条件下,两组均未显示出游离胆固醇的反馈调节。

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