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脑内注射血管活性肠肽对大鼠空肠丙氨酸吸收及胃酸分泌的影响。

Effects of intracerebral injections of VIP on jejunal alanine absorption and gastric acid secretion in rats.

作者信息

Saadé N E, Abdallah L E, Barada K A, Atweh S F, Nassar C F

机构信息

Department of Physiology, Faculty of Medicine, American University of Beirut, Lebanon.

出版信息

Regul Pept. 1995 Feb 14;55(3):269-76. doi: 10.1016/0167-0115(94)00115-e.

DOI:10.1016/0167-0115(94)00115-e
PMID:7761626
Abstract

The effects of intracerebral injections of VIP on jejunal alanine absorption and gastric acid secretion, and its association with vagal outflow were examined in Sprague-Dawley rats. Intracerebroventricular injection of VIP (2 ng) decreased significantly (P < 0.05) alanine absorption across the jejunum, whereas similar injections in vagotomized rats did not show further decrease in absorption beyond that noticed by vagotomy only. Moreover, VIP injected in the Nucleus Tractus Solitarius-Dorsal Motor Nucleus (NTS-DMN) complex (1 ng) produced also a significant inhibition of Ala absorption which was reduced but remained significant (P < 0.05) after vagotomy. Water movement was not affected by VIP injection in the lateral ventricle, while VIP injections in the NTS-DMN inhibited significantly (P < 0.05) jejunal water absorption by 10-12%. Vagotomy increased water absorption by 15-20% above control (P < 0.05) which was not altered by injecting VIP in the NTS-DMN complex. On the other hand, VIP injection in the NTS-DMN produced a 25.7% increase in gastric acid output in the first hour of the experiment followed by a non-significant decrease (P > 0.05) in the second hour. Same injections done in vagotomized animals produced similar effects to those elicited by vagotomy only. It can be suggested that NTS-DMN complex could be a site of action of VIP since injection of VIP in it produced a more pronounced inhibitory effect on water and Ala absorption than that produced by VIP injection in the LV. These effects were reduced or abolished by vagotomy.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在斯普拉格-道利大鼠中,研究了脑室内注射血管活性肠肽(VIP)对空肠丙氨酸吸收和胃酸分泌的影响,以及其与迷走神经传出的关系。脑室内注射VIP(2纳克)显著降低(P<0.05)空肠丙氨酸的吸收,而在迷走神经切断的大鼠中进行类似注射,吸收的降低幅度并未超过仅迷走神经切断时观察到的程度。此外,在孤束核-背运动核(NTS-DMN)复合体中注射VIP(1纳克)也显著抑制丙氨酸吸收,迷走神经切断后这种抑制作用减弱但仍显著(P<0.05)。侧脑室内注射VIP不影响水的转运,而在NTS-DMN中注射VIP显著(P<0.05)抑制空肠水吸收10%-12%。迷走神经切断使水吸收比对照增加15%-20%(P<0.05),在NTS-DMN复合体中注射VIP对此无改变。另一方面,在NTS-DMN中注射VIP在实验的第一小时使胃酸分泌增加25.7%,第二小时则无显著下降(P>0.05)。在迷走神经切断的动物中进行相同注射产生的效果与仅迷走神经切断时相似。可以推测,NTS-DMN复合体可能是VIP的作用位点,因为在其中注射VIP对水和丙氨酸吸收的抑制作用比在侧脑室注射VIP更明显。这些作用在迷走神经切断后减弱或消失。(摘要截断于250字)

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