کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2564117 | 1127604 | 2011 | 12 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Regulatory mechanism of duodenal bicarbonate secretion
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کلمات کلیدی
COXcGMPCFTRdbcAMPcNOSdbcGMP3′,5′-cyclic adenosine monophosphate - 3 '، 5'-cyclic adenosine monophosphate3′,5′-cyclic guanosine monophosphate - 3 '، 5'-cyclic guanosine monophosphatecAMP - cAMPadenylate cyclase - آدنیلات سیکلاسcyclooxygenase - آنزیم سیکلواکسیژنازcystic fibrosis transmembrane conductance regulator - رگولاتور رسانایی فرابنفش فیبروز کیستیکconstitutive nitric oxide synthase - سنتاز اکسید نیتریک پایدار
موضوعات مرتبط
علوم پزشکی و سلامت
داروسازی، سم شناسی و علوم دارویی
داروشناسی
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
The secretion of HCO3â in the duodenum is increased by exogenous prostaglandin (PG) E2 and mucosal acidification, the latter being accompanied by a rise in mucosal PGE2 content and nitric oxide (NO) release. The stimulatory effect of PGE2 is mediated intracellularly by both Ca2+ and 3â²,5â²-adenosine cyclic adenosine monophosphate (cAMP), and this action is inhibited by EP3 and EP4 antagonists. The secretion is also increased by NOR3 (NO donor), and this response is mimicked by dibutyryl 3â²,5â²-cyclic guanosine monophosphate (dbcGMP) and attenuated by indomethacin. Mucosal acidification stimulates HCO3â secretion with concomitant increases in mucosal PGE2 production and NO release. The effects on HCO3â secretion and PGE2 production are inhibited by indomethacin [nonselective cyclooxygenase (COX) inhibitor] and SC-560 (selective COX-1 inhibitor) but not rofecoxib (selective COX-2 inhibitor). NG-nitro-l-arginine methyl ester [l-NAME: nonselective NO synthase (NOS) inhibitor], but not aminoguanidine [selective inducible NOS inhibitor], attenuates the acid-induced HCO3â secretion and NO release in an l-arginine-sensitive manner. In addition, the response to PGE2 is potentiated by vinpocetine [phosphodiesterase (PDE) 1 inhibitor] and cilostamide (PDE3 inhibitor), while the response to NOR3 is increased by vinpocetine. We conclude that endogenous PGs and NO are both involved in the local regulation of acid-induced duodenal HCO3â secretion; COX-1 and constitutive NOS are key enzymes responsible for the production of PGs and NO, respectively; NO stimulates HCO3â secretion by increasing PG production; PGE2 stimulates HCO3â secretion via activation of EP3/EP4 receptors; and both PDE1 and PDE3 are involved in the regulation of duodenal HCO3â secretion.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Pharmacology & Therapeutics - Volume 130, Issue 1, April 2011, Pages 59-70
Journal: Pharmacology & Therapeutics - Volume 130, Issue 1, April 2011, Pages 59-70
نویسندگان
Koji Takeuchi, Kazutomo Kita, Shusaku Hayashi, Eitaro Aihara,