Hyun C S, Cragoe E J, Field M
Am J Physiol. 1985 Jul;249(1 Pt 1):C117-23. doi: 10.1152/ajpcell.1985.249.1.C117.
The role of alpha 2-adrenergic receptors in the regulation of intestinal Ca2+ transport was studied in vitro in rabbit proximal colon and distal ileum. Unidirectional mucosal-to-serosal and serosal-to-mucosal fluxes (Jm----s and Js----m) of 45Ca2+ were measured across isolated mucosal sheets bathed on both sides with identical Ringer solutions (1.25 mM Ca2+) and short-circuited. In the proximal colon, mucosal-to-epithelial influx (Jm----e) of Ca2+ was also determined. Proximal colonic mucosa secreted Ca2+ (in nmol X h-1 X cm-2, Jm----s = 12.1 and Js----m = 42.2). Epinephrine (10 microM) abolished Ca2+ secretion (Jm----s = 24.1 and Js----m = 24.9) but did not affect Jm----e (21.4 in controls and 23.6 after epinephrine). These effects were mediated by alpha 2-adrenergic receptors: yohimbine abolished the effect of epinephrine, but prazosin and propranolol did not; furthermore, clonidine mimicked the effects of epinephrine, whereas methoxamine and isoproterenol had no effect. Ileal mucosa did not transport Ca2+ spontaneously; epinephrine (10 microM) increased Jm----s in the ileum without affecting Js----m, thereby stimulating net Ca2+ absorption. The mechanism for these alpha 2-receptor-mediated effects was examined in proximal colon. The effect of epinephrine on Jm----s was dependent on serosal Na+ but was unaffected by ouabain or the Na+-Ca2+ exchange inhibitor, benzamil. The effect of epinephrine on Js----m was dependent on serosal Na+ and was blocked by both ouabain and benzamil. In the absence of epinephrine benzamil did not alter Jm----s or Js----m.(ABSTRACT TRUNCATED AT 250 WORDS)
在体外对兔近端结肠和远端回肠进行研究,以探讨α2 - 肾上腺素能受体在肠道Ca2+转运调节中的作用。用相同的林格氏溶液(1.25 mM Ca2+)双侧浸泡分离的黏膜片并使其短路,测量45Ca2+的单向黏膜到浆膜和浆膜到黏膜通量(Jm→s和Js→m)。在近端结肠中,还测定了Ca2+的黏膜到上皮内流(Jm→e)。近端结肠黏膜分泌Ca2+(以nmol·h-1·cm-2计,Jm→s = 12.1,Js→m = 42.2)。肾上腺素(10 μM)消除了Ca2+分泌(Jm→s = 24.1,Js→m = 24.9),但不影响Jm→e(对照组为21.4,肾上腺素处理后为23.6)。这些作用由α2 - 肾上腺素能受体介导:育亨宾消除了肾上腺素的作用,但哌唑嗪和普萘洛尔无此作用;此外,可乐定模拟了肾上腺素的作用,而甲氧明和异丙肾上腺素无作用。回肠黏膜不自发转运Ca2+;肾上腺素(10 μM)增加了回肠中的Jm→s,而不影响Js→m,从而刺激净Ca2+吸收。在近端结肠中研究了这些α2受体介导作用的机制。肾上腺素对Jm→s的作用依赖于浆膜Na+,但不受哇巴因或Na+-Ca2+交换抑制剂苄胺唑啉的影响。肾上腺素对Js→m的作用依赖于浆膜Na+,并被哇巴因和苄胺唑啉两者阻断。在无肾上腺素时,苄胺唑啉不改变Jm→s或Js→m。(摘要截短于250字)