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酪蛋白和β-酪蛋白吗啡对大鼠胃肠动力的影响。

Effect of casein and beta-casomorphins on gastrointestinal motility in rats.

作者信息

Daniel H, Vohwinkel M, Rehner G

机构信息

Institute of Nutrition, University of Giessen, West Germany.

出版信息

J Nutr. 1990 Mar;120(3):252-7. doi: 10.1093/jn/120.3.252.

Abstract

The effect of bovine casein and synthetic beta-casomorphins on the motility of rat gastrointestinal tract was studied by noninvasive techniques using the nonabsorbable marker 141Ce. Casein suspensions (CAS) or whey protein suspensions (WPS) were labeled with 141Ce and fed by gastric tube. Gastric emptying rate (GER) as well as gastrointestinal transit time (GITT) of the tracer were significantly longer with feeding CAS compared to WPS. The differences between the CAS and the WPS groups were partly (GER) or completely (GITT) abolished by pretreating the animals with the specific opiate-receptor antagonist naloxone. It is assumed that opioid peptides released from casein during digestion slowed gastrointestinal motility by direct interaction with gut opiate receptors. To prove whether beta-casomorphins, when given by gastric tube, can affect motility, different synthetic beta-casomorphins in doses between 1 and 10 mg were added to the WPS. The beta-casomorphin-4 (Tyr-Pro-Phe-Pro-NH2) showed no effect on GITT. The D-Ala substituted D-Ala-beta-casomorphin-4 (Tyr-D-Ala-Phe-Pro-NH2) and D-Ala-beta-casomorphin-5 (Tyr-D-Ala-Phe-D-Ala-Tyr-NH2), which are more resistant to proteolytic attack and have higher opioid potency than beta-casomorphin-4, slowed GITT in a dose-dependent manner.

摘要

采用不可吸收标记物141Ce,运用非侵入性技术研究了牛酪蛋白和合成β-酪蛋白吗啡对大鼠胃肠道运动的影响。酪蛋白悬液(CAS)或乳清蛋白悬液(WPS)用141Ce标记后经胃管喂食。与WPS相比,喂食CAS后示踪剂的胃排空率(GER)以及胃肠道转运时间(GITT)显著延长。用特异性阿片受体拮抗剂纳洛酮预处理动物后,CAS组和WPS组之间的差异部分(GER)或完全(GITT)消除。据推测,酪蛋白在消化过程中释放的阿片肽通过与肠道阿片受体直接相互作用减缓了胃肠蠕动。为了证明经胃管给予β-酪蛋白吗啡是否会影响胃肠蠕动,在WPS中添加了剂量为1至10 mg的不同合成β-酪蛋白吗啡。β-酪蛋白吗啡-4(Tyr-Pro-Phe-Pro-NH2)对GITT无影响。D-Ala取代的D-Ala-β-酪蛋白吗啡-4(Tyr-D-Ala-Phe-Pro-NH2)和D-Ala-β-酪蛋白吗啡-5(Tyr-D-Ala-Phe-D-Ala-Tyr-NH2)比β-酪蛋白吗啡-4对蛋白水解攻击更具抗性且阿片效力更高,它们以剂量依赖的方式减缓了GITT。

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