Gulley Stephen, Sharma Sanjay K, Moran Timothy H, Sayegh Ayman I
Gastroenterology Laboratory, Department of Biomedical Sciences, College of Veterinary Medicine, Tuskegee University, Tuskegee, AL 36088, USA.
Peptides. 2005 Sep;26(9):1617-22. doi: 10.1016/j.peptides.2005.02.020. Epub 2005 Mar 17.
To examine the role of cholecystokinin1 receptor (CCK1) in the activation of brainstem and myenteric neurons by CCK, we compared the ability of exogenous CCK-8 to induce Fos-like immunoreactivity (Fos-LI) in these neurons in Otsuka Long-Evans Tokushima Fatty (OLETF) rats, lacking CCK1 receptors, and Long-Evans Tokushima Otsuka (LETO) controls. Five groups (n=4 rats per group) of OLETF rats, and five LETO control groups, were injected intraperitoneally (IP) with 5, 10, 20, and 40 microg/kg CCK-8 or saline. Forty-micrometer brainstem sections containing the area postrema, nucleus of the solitary tract, and the dorsal motor nucleus of the vagus, and myenteric neurons of the duodenum, jejunum, and ileum underwent a diaminobenzidine reaction enhanced with nickel to reveal Fos-LI. CCK-8 did not increase Fos-LI in any of the tested neurons in the OLETF rats. CCK-8 increased Fos-LI in the brainstem of the LETO rats in a dose dependent manner. In the LETO rats only 40 microg/kg CCK-8 increased Fos-LI in the myenteric plexus of the jejunum. This study demonstrates that CCK-8 activates the brainstem and myenteric neurons through the CCK1 receptor.
为研究胆囊收缩素1受体(CCK1)在胆囊收缩素激活脑干和肠肌间神经元中的作用,我们比较了外源性CCK - 8在缺乏CCK1受体的大冢长 - 伊文斯 - 德岛肥胖(OLETF)大鼠和大冢长 - 伊文斯 - 德岛对照(LETO)大鼠的这些神经元中诱导Fos样免疫反应性(Fos - LI)的能力。将五组(每组n = 4只大鼠)OLETF大鼠和五组LETO对照大鼠腹腔注射(IP)5、10、20和40μg / kg CCK - 8或生理盐水。对包含最后区、孤束核和迷走神经背运动核的40微米脑干切片以及十二指肠、空肠和回肠的肠肌间神经元进行用镍增强的二氨基联苯胺反应以显示Fos - LI。CCK - 8在OLETF大鼠的任何测试神经元中均未增加Fos - LI。CCK - 8在LETO大鼠的脑干中以剂量依赖性方式增加Fos - LI。在LETO大鼠中,仅40μg / kg CCK - 8增加了空肠肠肌丛中的Fos - LI。本研究表明CCK - 8通过CCK1受体激活脑干和肠肌间神经元。