| کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن | 
|---|---|---|---|---|
| 8348519 | 1541728 | 2014 | 5 صفحه PDF | دانلود رایگان | 
عنوان انگلیسی مقاله ISI
												Intravenous infusion of gastrin-releasing peptide-27 and bombesin in rats reveals differential effects on meal size and intermeal interval length
												
											ترجمه فارسی عنوان
													تزریق داخل وریدی پپتید-27 آزاد کننده گاسترین و بمبسین در موش صحرایی اثرات متفاوتی بر میزان غذا و طول فاصله بین دوره ای نشان می دهد 
													
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																																												کلمات کلیدی
												
											موضوعات مرتبط
												
													علوم زیستی و بیوفناوری
													بیوشیمی، ژنتیک و زیست شناسی مولکولی
													 زیست شیمی
												
											چکیده انگلیسی
												We have previously shown that the intraperitoneal (i.p.) administration of gastrin-releasing peptide-27 (GRP-27) or bombesin (BN) (at 0.21, 0.41 and 1.03 nmol/kg) reduces meal size (MS) and prolongs the intermeal interval (IMI). Here, we hypothesized that the intravenous (i.v.) administration of the same doses of GRP-27 and BN will be as effective as the i.p. administration in evoking these feeding responses. To test this hypothesis, we administered GRP-27 and BN i.v. and measured first MS (10% sucrose), IMI, satiety ratio (SR, IMI/MS) and second MS in overnight food-deprived but not water-deprived male Sprague Dawley rats. We found that (1) only GRP-27 reduced the first MS, (2) BN prolonged the IMI, (3) GRP-27 and BN increased the SR and (4) only BN reduced the size of the second meal. Contrary to our hypothesis, the i.v. administration of GRP-27 and BN affected the MS and IMI differently than did the i.p. administration. In conclusion, this pharmacological study suggests that the MS and IMI are regulated at different sites.
											ناشر
												Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Peptides - Volume 51, January 2014, Pages 145-149
											Journal: Peptides - Volume 51, January 2014, Pages 145-149
نویسندگان
												Martha C. Washington, Sarah Salyer, Amnah H. Aglan, Ayman I. Sayegh, 
											