Suppr超能文献

拟交感神经药对大鼠胃体内和体外胃酸分泌影响的比较。

A comparison of the effects of sympathomimetic agents on gastric acid secretion by the rat stomach in vivo and in vitro.

作者信息

Canfield S P, Price C A

出版信息

J Physiol. 1981 Jul;316:11-21. doi: 10.1113/jphysiol.1981.sp013768.

Abstract
  1. The action of isoprenaline on gastric acid secretion in rats with Heidenhain pouches has been compared with its action in a rat isolated stomach preparation. 2. Isoprenaline (40 micrograms kg-1 h-1) inhibited the acid secretion in response to pentagastrin (20 micrograms kg-1 h-1) in conscious rate with Heidenhain pouches. 3. This inhibition could be abolished by propranolol (2 mg kg-1) and butoxamine (8 mg kg-1) and partially reversed by practolol (8 mg kg-1). 4. Propranolol (2 mg kg-1) significantly increased the response to pentagastrin (20 micrograms kt-1 h-1) but butoxamine and practolol (both at 8 mg kg-1) and the inactive isomer (+)-propranolol (2 mg kg-1) were without any effect on the pentagastrin response in the rats with pouches. 5. In the rat isolated stomach preparation isoprenaline stimulated acid secretion over the range 10(-7) M-10(-3) M whereas phenylephrine and methoxamine were without effect. 6. Propranolol (2 X 10(-5) M) inhibited this stimulatory effect of isoprenaline in vitro but (+)-propranolol (2 X 10(-5) M), practolol and butoxamine (both at 10(-4) M) had no effect on the response. 7. Propranolol (2 X 10(-5) M) did not have any effect on the response of the isolated stomach to pentagastrin (5 X 10(-7) M) or bethanechol (1.7 X 10(-5) M). 8. Phenylephrine (2 X 10(-5) M) did not affect the in vitro responses to pentagastrin (2.17 X 10(-7) M), bethanechol (1.7 X 10(-5) M) or histamine (5.4 X 10(-5) M). 9. It is concluded that isoprenaline has a direct stimulatory effect and an indirect inhibitory effect on gastric acid secretion in the rat. Both effects involve stimulation of beta-adrenoceptors. The relative predominance of one or other of these two opposing effects may help to explain the contradictory results in the literature regarding the actions of beta-adrenoceptor agonists on gastric acid secretion.
摘要
  1. 已将异丙肾上腺素对海登海因小胃大鼠胃酸分泌的作用与其对大鼠离体胃制备物的作用进行了比较。2. 异丙肾上腺素(40微克/千克·小时)抑制了有海登海因小胃的清醒大鼠对五肽胃泌素(20微克/千克·小时)的胃酸分泌反应。3. 普萘洛尔(2毫克/千克)和布托沙明(8毫克/千克)可消除这种抑制作用,而醋丁洛尔(8毫克/千克)可部分逆转这种抑制作用。4. 普萘洛尔(2毫克/千克)显著增加了对五肽胃泌素(20微克/千克·小时)的反应,但布托沙明和醋丁洛尔(均为8毫克/千克)以及无活性的异构体(+)-普萘洛尔(2毫克/千克)对有小胃的大鼠的五肽胃泌素反应没有任何影响。5. 在大鼠离体胃制备物中,异丙肾上腺素在10^(-7)M - 10^(-3)M范围内刺激胃酸分泌,而苯肾上腺素和甲氧明则无作用。6. 普萘洛尔(2×10^(-5)M)在体外抑制了异丙肾上腺素的这种刺激作用,但(+)-普萘洛尔(2×10^(-5)M)、醋丁洛尔和布托沙明(均为10^(-4)M)对该反应无作用。7. 普萘洛尔(2×10^(-5)M)对离体胃对五肽胃泌素(5×10^(-7)M)或氨甲酰甲胆碱(1.7×10^(-5)M)的反应没有任何影响。8. 苯肾上腺素(2×10^(-5)M)不影响对五肽胃泌素(2.17×10^(-7)M)、氨甲酰甲胆碱(1.7×10^(-5)M)或组胺(5.4×10^(-5)M)的体外反应。9. 得出结论:异丙肾上腺素对大鼠胃酸分泌有直接刺激作用和间接抑制作用。这两种作用均涉及β-肾上腺素能受体的刺激。这两种相反作用中一种或另一种的相对优势可能有助于解释文献中关于β-肾上腺素能受体激动剂对胃酸分泌作用的矛盾结果。

相似文献

引用本文的文献

1
Effects of dipyrone on the digestive tract.安乃近对消化道的影响。
Braz J Med Biol Res. 2019 Jan 10;52(2):e8103. doi: 10.1590/1414-431X20188103.

本文引用的文献

1
Preparation of chronic denervated gastric pouches in the rat.大鼠慢性去神经支配胃袋的制备
Am J Physiol. 1959 Aug;197:257-9. doi: 10.1152/ajplegacy.1959.197.2.257.
6
Effects of propranolol on gastric secretion in albino rats.普萘洛尔对白化病大鼠胃液分泌的影响。
Br J Pharmacol. 1974 Jun;51(2):213-6. doi: 10.1111/j.1476-5381.1974.tb09649.x.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验