Kaouass M, Deloyer P, Dandrifosse G
Department of Biochemistry and General Physiology, Chemistry Institute, Liege, Belgium.
J Endocrinol. 1997 Jun;153(3):429-36. doi: 10.1677/joe.0.1530429.
In this study we investigated whether brain-gut peptides are implicated in the activation of the hypophysial-adrenal axis (HAA) in suckling rats treated orally with spermine. The first group of rats received i.p. injections of bombesin, vasoactive intestinal polypeptide (VIP), somatostatin or neurotensin, starting on day 11 of life, and killed on day 14. The small intestine was removed and analysed for its content of proteins, DNA, polyamines and for its specific activity (SA) of disaccharidases. The second group of rats received one of the hormones cited above and was killed 45 min after the treatment for determination of corticosterone plasma concentration. Rats of the third group were adrenalectomised then treated with bombesin as the first group. The fourth group of rats was orally treated with spermine and sacrificed 2, 3, 4, 6 and 8 h thereafter for analysis of plasma and intestinal concentrations of bombesin. The i.p. injection of bombesin increased the sucrase and maltase SA in the whole small intestine, while it decreased the lactase SA in the distal part. Intestinal weight and length, contents of DNA, protein, spermidine and spermine, and corticosterone plasma levels were enhanced by bombesin treatment. Somatostatin, neurotensin and VIP were ineffective on all the parameters studied. Adrenalectomy, in bombesin-treated rats, decreased the sucrase and maltase SA in the whole intestine, and decreased the lactase SA in the proximal intestine. It has no effect on intestinal weight and length, and protein content. Oral administration of spermine had no effect on plasma concentration of bombesin, whereas it decreased the content of this peptide in the whole small intestine. It is possible that bombesin may control intestinal development in suckling rats and be a link between the ingestion of spermine and the liberation of corticosterone by the adrenal glands.
在本研究中,我们调查了脑肠肽是否参与了经口给予精胺的乳鼠垂体-肾上腺轴(HAA)的激活过程。第一组大鼠从出生第11天开始腹腔注射蛙皮素、血管活性肠肽(VIP)、生长抑素或神经降压素,并于第14天处死。取出小肠,分析其蛋白质、DNA、多胺含量以及双糖酶的比活性(SA)。第二组大鼠接受上述一种激素处理,并在处理后45分钟处死,以测定血浆皮质酮浓度。第三组大鼠进行肾上腺切除,然后像第一组一样用蛙皮素处理。第四组大鼠经口给予精胺,然后在2、3、4、6和8小时后处死,以分析血浆和小肠中蛙皮素的浓度。腹腔注射蛙皮素可增加整个小肠中蔗糖酶和麦芽糖酶的SA,而降低远端小肠中乳糖酶的SA。蛙皮素处理可增加小肠重量和长度、DNA、蛋白质、亚精胺和精胺含量以及血浆皮质酮水平。生长抑素、神经降压素和VIP对所有研究参数均无作用。在经蛙皮素处理的大鼠中,肾上腺切除降低了整个小肠中蔗糖酶和麦芽糖酶的SA,并降低了近端小肠中乳糖酶的SA。它对小肠重量和长度以及蛋白质含量没有影响。口服精胺对血浆蛙皮素浓度没有影响,而降低了整个小肠中该肽的含量。蛙皮素可能控制乳鼠的肠道发育,并且是精胺摄入与肾上腺释放皮质酮之间的一个联系。