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血管活性肠肽、生长抑素、神经降压素、八肽胆囊收缩素及促胰液素对大鼠肠道氨基酸吸收的影响

Effect of vasoactive intestinal peptide, somatostatin, neurotensin, cholecystokinin octapeptide, and secretin on intestinal absorption of amino acid in rat.

作者信息

Chen Y F, Feng Z T, Wen S H, Lu G J

机构信息

Department of Medicine, Peking Union Medical College, Beijing, China.

出版信息

Dig Dis Sci. 1987 Oct;32(10):1125-9. doi: 10.1007/BF01300199.

Abstract

The effects of vasoactive intestinal peptide (VIP), somatostatin (SRIF), neurotensin (NT), cholecystokinin octapeptide (CCK-8), and secretin (SEC) on the intestinal absorption of amino acid were investigated. Six groups of Wistar rats were studied: (1) controls; (2) VIP treated; (3) SRIF treated; (4) NT treated; (5) CCK-8 treated; (6) SEC treated. [3H]Leucine was given intraluminally through a cannula at the ligament of Treitz, a number of blood samples were obtained through a superior mesenteric vein catheter 1-60 min after administration of [3H]leucine, and the radioactivity of plasma was measured to evaluate the absorption of [3H]leucine. It was shown that VIP and SRIF significantly inhibited the absorption of [3H]leucine (by 59.1% and 38.7%, respectively), whereas NT, CCK-8, and SEC significantly enhanced absorption (by 44.2%, 49.6%, and 39.1%, respectively). Radioimmunoassays of VIP, SRIF, and NT showed that at least some of the hormones or peptides exerted their effects on absorption of leucine at or near their physiological concentrations.

摘要

研究了血管活性肠肽(VIP)、生长抑素(SRIF)、神经降压素(NT)、八肽胆囊收缩素(CCK - 8)和促胰液素(SEC)对氨基酸肠道吸收的影响。对六组Wistar大鼠进行了研究:(1)对照组;(2)VIP处理组;(3)SRIF处理组;(4)NT处理组;(5)CCK - 8处理组;(6)SEC处理组。通过在屈氏韧带处的插管将[³H]亮氨酸腔内给药,在给予[³H]亮氨酸后1 - 60分钟,通过肠系膜上静脉导管采集多个血样,并测量血浆的放射性以评估[³H]亮氨酸的吸收情况。结果表明,VIP和SRIF显著抑制[³H]亮氨酸的吸收(分别抑制59.1%和38.7%),而NT、CCK - 8和SEC显著增强吸收(分别增强44.2%、49.6%和39.1%)。对VIP、SRIF和NT的放射免疫分析表明,至少某些激素或肽在其生理浓度或接近生理浓度时对亮氨酸的吸收发挥作用。

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