• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

Development of gallbladder contractility in the guinea pig.

作者信息

Denehy C M, Ryan J R

出版信息

Pediatr Res. 1986 Mar;20(3):214-7. doi: 10.1203/00006450-198603000-00003.

DOI:10.1203/00006450-198603000-00003
PMID:3703610
Abstract

In vitro experiments were performed to examine the contractile responsiveness of guinea pig gallbladder smooth muscle as a function of developmental age. Gallbladder muscle strips from preterm (day 50-55 gestation), newborn (days 1-3 post partum), and 1-month-old animals were stimulated with agonists that initiate the contractile process either by activation of membrane receptors (acetylcholine and the octapeptide of cholecystokinin) or by membrane depolarization (potassium). Dose-response curves were constructed for each agonist in each age group and analyzed with respect to the maximal force developed and the pD2 value (negative logarithm of the dose of agonist which produces a one-half maximal response). The results can be summarized as follows: 1) when normalized for tissue cross-sectional area, the magnitude of the contractile response to each agonist increased with increasing developmental age; 2) the dose of agonist required to elicit a one-half maximal response was independent of developmental age. The data indicate that cholinergic and cholecystokinin receptors are present and functional on gallbladder smooth muscle prior to birth and that the force generating capacity of the tissue continues to develop after birth. A reduced contractility of the gallbladder in preterm and newborn animals as compared to young adults may partially explain the decreased choledochol bile flow seen in the neonate.

摘要

相似文献

1
Development of gallbladder contractility in the guinea pig.
Pediatr Res. 1986 Mar;20(3):214-7. doi: 10.1203/00006450-198603000-00003.
2
Effect of pregnancy on gallbladder contractility in the guinea pig.妊娠对豚鼠胆囊收缩性的影响。
Gastroenterology. 1984 Sep;87(3):674-8.
3
Response to calcium of skinned gallbladder smooth muscle from newborn and adult guinea pigs.新生豚鼠和成年豚鼠去皮胆囊平滑肌对钙的反应。
Pediatr Res. 1990 Oct;28(4):336-8. doi: 10.1203/00006450-199010000-00007.
4
Effect of progesterone pretreatment on guinea pig gallbladder motility in vitro.孕酮预处理对豚鼠离体胆囊运动的影响。
Gastroenterology. 1982 Jul;83(1 Pt 1):81-3.
5
A comparison of the effects of various sex steroids on cholecystokinin- and KCl-induced tension in female guinea pig gallbladder strips.比较各种性激素对雌性豚鼠胆囊带中胆囊收缩素和 KCl 诱导张力的影响。
Gen Comp Endocrinol. 2013 May 1;185:37-43. doi: 10.1016/j.ygcen.2013.01.012. Epub 2013 Feb 8.
6
The basis for progesterone impairment of gallbladder contractility in male guinea pigs in vitro.
J Surg Res. 1998 Oct;79(2):97-102. doi: 10.1006/jsre.1998.5407.
7
Calcium and gallbladder smooth muscle contraction in the guinea pig: effect of pregnancy.
Gastroenterology. 1985 Dec;89(6):1279-85. doi: 10.1016/0016-5085(85)90643-2.
8
Influence of progesterone on guinea pig gallbladder motility in vitro.
Dig Dis Sci. 1986 May;31(5):513-8. doi: 10.1007/BF01320317.
9
Actions of genistein on contractile response of smooth muscle isolated from guinea pig gallbladder.染料木黄酮对豚鼠胆囊平滑肌收缩反应的作用。
Hepatobiliary Pancreat Dis Int. 2009 Dec;8(6):614-9.
10
Developmental changes in gastric fundus smooth muscle contractility and involvement of extracellular calcium in fetal and adult guinea pigs.
Pediatr Res. 1994 Nov;36(5):642-6. doi: 10.1203/00006450-199411000-00019.

引用本文的文献

1
Mechanisms of Parenteral Nutrition-Associated Liver and Gut Injury.肠外营养相关肝损伤和肠损伤的机制。
Nutr Clin Pract. 2020 Feb;35(1):63-71. doi: 10.1002/ncp.10461. Epub 2019 Dec 23.
2
Biliary motility.胆道动力
Gut. 1990 May;31(5):571-82. doi: 10.1136/gut.31.5.571.