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对乳鼠进行肠内注射肥胖抑制素对肠道收缩性的影响。

The influence of enteral obestatin administration to suckling rats on intestinal contractility.

作者信息

Słupecka M, Grzesiak P, Kwiatkowski J, Gajewska M, Kuwahara A, Kato I, Woliński J

机构信息

Department of Animal Physiology, The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, Jabłonna, Poland.

Department of Animal Physiology, The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, Jabłonna, Poland.

出版信息

Gen Comp Endocrinol. 2017 Jul 1;248:69-78. doi: 10.1016/j.ygcen.2017.02.006. Epub 2017 Feb 16.

Abstract

This study investigated the effect of enteral administration of obestatin on the contractility of whole-thickness preparations of duodenum and middle jejunum, as well as on the morphology of the enteric nervous system (ENS). Suckling rats were assigned to 3 groups (n=12) treated with: C-saline solution; LO-obestatin (125nmol/kgb.wt); HO-obestatin (250nmol/kgb.wt). Saline solution or obestatin were administered twice daily, from the 14th to the 21st day of life. Sections were studied in an organ bath, for isometric recording in the presence of acetylocholine (ACh), atropine (ATR) and tetradotoxin (TTX). Thickness of intestinal muscularis layer, the number of interstitial cells of Cajal (ICC) were measured in the paraffin sections. The immunodetection of Muscarinic Acetylocholine Receptor 2 (M2 receptor) was performed in the intestinal segments. In both intestinal segments HO treatment decreased the amplitude of spontaneous contraction compared to that observed in the C group. In the middle jejunum, the LO treatment also decreased the amplitude. TTX and ATR had no effect on amplitude of spontaneous contraction in the jejunum of LO and HO-treated animals. Compared to the C group, duodenal sections from HO animals and middle jejunum sections from LO and HO groups displayed a lower amplitude in response to ACh and EFS evoked contraction. An increase in the thickness of the muscularis layer was observed in the duodenum of LO and HO groups whereas the number ICC did not change significantly after treatment with obestatin. Moreover, the enteral administration of obestatin did not effect significantly on the cytoplasmic expression of M2 receptor in the jejunum. Our study demonstrated that enteral administration of obestatin to suckling rats influences small intestine contractility in the segment specific manner.

摘要

本研究调查了肠内给予肥胖抑制素对十二指肠和空肠中段全层标本收缩性以及对肠神经系统(ENS)形态的影响。将乳鼠分为3组(每组n = 12),分别给予:C组 - 生理盐水溶液;低剂量组 - 肥胖抑制素(125nmol/kg体重);高剂量组 - 肥胖抑制素(250nmol/kg体重)。从出生后第14天至21天,每天两次给予生理盐水溶液或肥胖抑制素。在器官浴中研究切片,在乙酰胆碱(ACh)、阿托品(ATR)和河豚毒素(TTX)存在的情况下进行等长记录。在石蜡切片中测量肠肌层厚度、Cajal间质细胞(ICC)数量。在肠段进行毒蕈碱型乙酰胆碱受体2(M2受体)的免疫检测。与C组相比,在两个肠段中,高剂量组处理均降低了自发收缩的幅度。在空肠中段,低剂量组处理也降低了幅度。TTX和ATR对低剂量组和高剂量组处理动物空肠的自发收缩幅度没有影响。与C组相比,高剂量组动物的十二指肠切片以及低剂量组和高剂量组的空肠中段切片对ACh和电场刺激(EFS)诱发收缩的反应幅度较低。在低剂量组和高剂量组的十二指肠中观察到肌层厚度增加,而用肥胖抑制素处理后ICC数量没有显著变化。此外,肠内给予肥胖抑制素对空肠中M2受体的细胞质表达没有显著影响。我们的研究表明,对乳鼠肠内给予肥胖抑制素以节段特异性方式影响小肠收缩性。

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