Faculty of Medicine, National Yang-Ming University School of Medicine, Taipei, Taiwan.
Peptides. 2010 Jun;31(6):1113-7. doi: 10.1016/j.peptides.2010.03.024. Epub 2010 Mar 23.
Obestatin, a novel putative 23-amino acid peptide, is derived from mammalian preproghrelin gene via a bioinformatics approach. Although obestatin regulates thirst, sleep, memory, anxiety, activates cortical neurons in the brain and stimulate proliferation of retinal pigment epithelial cells, there is no study to explore its central impacts on the lower gut motility and secretion. We investigated the influence of intracerebroventricular (ICV) injection of obestatin on rat colonic motor and secretory functions. Colonic transit time, fecal pellet output and fecal content were assessed in freely fed, conscious rats, which were implanted with ICV and colonic catheters chronically. Human/rat corticotropin-releasing factor (h/rCRF) was applied as a stimulatory inducer of colonic motility and secretion. ICV injection of obestatin (0.1, 0.3, 1.0 nmol/rat) did not modify the colonic transit time, whereas ICV injection of h/rCRF (0.3 nmol/rat) significantly shortened colonic transit time. ICV obestatin in any dose we tested did not affect the fecal pellet output, frequency of watery diarrhea, total fecal weight, fecal dried solid weight, or fecal fluid weight in the first hour post-injection, either. In contrast, ICV injection of h/rCRF effectively stimulated fecal pellet output, as well as increased total fecal weight, fecal dried solid weight and fecal fluid weight during the first hour post-injection, compared to ICV saline controls. In conclusion, using our novel simultaneous measurement method, acutely central administration of obestatin exhibits no influence on colonic motility and secretion in conscious rats.
肥胖抑制素,一种新的 23 个氨基酸肽,通过生物信息学方法从哺乳动物前胃饥饿素基因衍生而来。虽然肥胖抑制素调节口渴、睡眠、记忆、焦虑,激活大脑皮层神经元,并刺激视网膜色素上皮细胞增殖,但没有研究探索其对下肠道运动和分泌的中枢影响。我们研究了脑室内(ICV)注射肥胖抑制素对大鼠结肠运动和分泌功能的影响。在自由喂养、清醒的大鼠中评估了结肠传输时间、粪便颗粒输出和粪便含量,这些大鼠被慢性植入了 ICV 和结肠导管。人类/大鼠促肾上腺皮质释放因子(h/rCRF)被用作刺激结肠运动和分泌的诱导剂。ICV 注射肥胖抑制素(0.1、0.3、1.0 nmol/大鼠)不会改变结肠传输时间,而 ICV 注射 h/rCRF(0.3 nmol/大鼠)显著缩短了结肠传输时间。我们测试的任何剂量的 ICV 肥胖抑制素都不会影响粪便颗粒输出、水样腹泻频率、总粪便重量、粪便干燥固体重量或注射后 1 小时内的粪便流体重量。相比之下,与 ICV 盐水对照相比,ICV 注射 h/rCRF 有效地刺激了粪便颗粒输出,并增加了总粪便重量、粪便干燥固体重量和注射后 1 小时内的粪便流体重量。总之,使用我们的新型同步测量方法,急性中枢给予肥胖抑制素对清醒大鼠的结肠运动和分泌没有影响。