Depoortere I, Peeters T L, Vantrappen G
Department of Medical Research, Katholieke Universiteit Leuven, Belgium.
Gastroenterology. 1990 Sep;99(3):652-8. doi: 10.1016/0016-5085(90)90951-v.
The development of the motilin receptor was studied through contraction and binding studies of groups of three rabbits aged between 2 and 289 days. The contractility of small intestinal smooth muscle strips was measured isotonically. The aborally decreasing gradient in response to motilin, known to exist in adult rabbits, was already present at day 8 (maximum contractile responses expressed as a percent of the maximal response to acetylcholine were 77% +/- 9%, 34% +/- 10%, and 25% +/- 8% for duodenal, jejunal, and ileal strips, respectively). Throughout the observation period, the doses of motilin and its agonist erythromycin that were required to induce 50% of the response remained constant and were not significantly different from doses required for adults (their negative logarithms were 8.55 +/- 0.35 and 5.70 +/- 0.25, respectively). The correlation between the maximum contractile response toward motilin and erythromycin was almost perfect (r2 = 0.82). Binding studies with iodinated norleucine13-porcine motilin were performed using antral smooth muscle tissue homogenates. The maximum number of binding sites increased rapidly after 8 days (3.3 +/- 0.4 fmol/mg protein) and reached a peak at 21 days (20.7 +/- 1.4 fmol/mg protein), but decreased at that point toward the adult value (40 days, 10.6 +/- 1.3; 289 days, 9.8 +/- 1.1 fmol/mg protein). The dissociation constant, however, remained unchanged. The peak value of receptor density occurred at about the time that the rate of increase of the length of the intestine and of the weight of the antrum were at maximum levels (at 18 and 27 days, respectively). Motilin receptors are expressed early postnatally, and the regional gradient in sensitivity towards motilin is also established soon after birth. If applicable to humans, an early response to erythromycin may have therapeutic value.
通过对3组年龄在2至289天之间的兔子进行收缩和结合研究,对胃动素受体的发育情况展开了研究。采用等张法测量小肠平滑肌条的收缩性。已知成年兔子存在对胃动素的向肛递减梯度,在第8天就已出现(十二指肠、空肠和回肠平滑肌条对胃动素的最大收缩反应分别表示为对乙酰胆碱最大反应的百分比,依次为77%±9%、34%±10%和25%±8%)。在整个观察期内,诱导50%反应所需的胃动素及其激动剂红霉素的剂量保持恒定,且与成年兔子所需剂量无显著差异(其负对数分别为8.55±0.35和5.70±0.25)。对胃动素和红霉素的最大收缩反应之间的相关性几乎是完美的(r2 = 0.82)。使用胃窦平滑肌组织匀浆进行了用碘化正亮氨酸13 - 猪胃动素的结合研究。结合位点的最大数量在8天后迅速增加(3.3±0.4 fmol/mg蛋白质),并在21天达到峰值(20.7±1.4 fmol/mg蛋白质),但此后降至成年值(40天,10.6±1.3;289天,9.8±1.1 fmol/mg蛋白质)。然而,解离常数保持不变。受体密度的峰值大约出现在肠道长度和胃窦重量增加速率达到最大值的时候(分别在18天和27天)。胃动素受体在出生后早期就有表达,并且对胃动素的敏感性区域梯度在出生后不久也已建立。如果对人类也适用,那么对红霉素的早期反应可能具有治疗价值。