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垂体切除术后胆固醇肠道吸收显著增加,甲状腺激素可使其恢复正常。

Dramatically increased intestinal absorption of cholesterol following hypophysectomy is normalized by thyroid hormone.

作者信息

Gälman Cecilia, Bonde Ylva, Matasconi Manuela, Angelin Bo, Rudling Mats

机构信息

Karolinska Institute, Center for Endocrinology, Metabolism, and Diabetes, Department of Medicine and Molecular Nutrition Unit, Center for Nutrition and Toxicology, Karolinska University Hospital, Huddinge, S-141 86 Stockholm, Sweden.

出版信息

Gastroenterology. 2008 Apr;134(4):1127-36. doi: 10.1053/j.gastro.2008.01.032. Epub 2008 Jan 17.

Abstract

BACKGROUND & AIMS: Hypopituitarism is associated with dyslipidemia, and feeding hypophysectomized rats cholesterol induces severe hypercholesterolemia. This study aimed to unravel further how hypophysectomy alters cholesterol and bile acid metabolism.

METHODS

Intact and hypophysectomized rats were studied during challenge with dietary cholesterol and ezetimibe and upon hormonal substitution with growth hormone, cortisone, and thyroid hormone.

RESULTS

Five findings were established in hypophysectomized rats: (1) The intestinal absorption of cholesterol is doubled. (2) Treatment with ezetimibe abolishes the increases in serum and liver cholesterol. (3) Only thyroid hormone treatment normalizes the increased absorption of cholesterol. (4) The intestinal gene expression of cholesterol transporters NPC1L1 and ABCG5/G8 is unaltered, whereas the hepatic expression of ABCG5/G8 is diminished but strongly stimulated by thyroid hormone. The latter mechanism was supported by measurements of biliary cholesterol and of fecal neutral steroids. (5) The reduced hepatic expression of ABCG5/G8 and Cyp7a1 was normalized by cholesterol feeding, suggesting that other nonestablished mechanisms under pituitary control are important to maintain rats resistant to dietary cholesterol.

CONCLUSIONS

The intestinal absorption of dietary cholesterol is under pituitary control largely exerted by thyroid hormone. Hepatic secretion of cholesterol and ABCG5/G8 expression are strongly stimulated in hypophysectomized rats during treatment with thyroid hormone.

摘要

背景与目的

垂体功能减退与血脂异常有关,给垂体切除的大鼠喂食胆固醇会导致严重的高胆固醇血症。本研究旨在进一步揭示垂体切除如何改变胆固醇和胆汁酸代谢。

方法

对完整和垂体切除的大鼠进行研究,期间给予饮食胆固醇和依泽替米贝进行挑战,并给予生长激素、可的松和甲状腺激素进行激素替代。

结果

在垂体切除的大鼠中发现了五个结果:(1)胆固醇的肠道吸收增加了一倍。(2)用依泽替米贝治疗可消除血清和肝脏胆固醇的升高。(3)只有甲状腺激素治疗能使增加的胆固醇吸收恢复正常。(4)胆固醇转运蛋白NPC1L1和ABCG5/G8的肠道基因表达未改变,而ABCG5/G8的肝脏表达减少,但受到甲状腺激素的强烈刺激。胆汁胆固醇和粪便中性类固醇的测量支持了后一种机制。(5)通过喂食胆固醇使肝脏中ABCG5/G8和Cyp7a1表达的降低恢复正常,这表明垂体控制下的其他未确定机制对于维持大鼠对饮食胆固醇的抗性很重要。

结论

饮食中胆固醇的肠道吸收受垂体控制,主要由甲状腺激素发挥作用。在垂体切除的大鼠中,用甲状腺激素治疗期间,胆固醇的肝脏分泌和ABCG5/G8表达受到强烈刺激。

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