Kandasamy S B
Radiation Pathophysiology and Toxicology Department, Armed Forces Radiobiology Research Institute, Bethesda, Maryland 20889-5603, USA.
Radiat Res. 1998 Sep;150(3):298-303.
This study was designed to identify the mechanisms underlying the reduction in food intake in rats. Measurements were made of the release of cholecystokinin (CCK) stimulated by potassium chloride in the hypothalamus after (a) gamma irradiation (60Co), (b) treatment with the CCK-A and CCK-B antagonists L-364,718 and L-365,260 with and without radiation, (c) bilateral abdominal vagotomy, and (d) vagotomy with and without radiation and with and without L-364,718. The concentrations of CCK in hypothalamus perfusate were measured by a radioimmunoassay. Exposure of rats to 1, 3, 5 and 10 Gy (1 Gy/min) increased release of CCK in the hypothalamus in a manner that was dependent on dose. A dose of 5 Gy was chosen for further studies. Intraperitoneal (i.p.) administration of 10, 20 and 50 microg/kg of L-364,718 did not induce significant changes in release of CCK in sham-irradiated animals. However, the drug decreased the release of CCK induced by radiation in a dose-dependent manner. In contrast to L-364,718, 20-50 microg/kg of L-365,260 decreased the release of CCK in the hypothalamus in sham-irradiated animals but did not decrease release of CCK induced by exposure to radiation. Vagotomy produced an insignificant reduction in release of CCK compared to that in sham-irradiated controls. However, vagotomy decreased release of CCK in irradiated rats compared to the irradiated rats without vagotomy. Vagotomy and i.p. administration of 10, 20 and 50 microg/kg of L-364,718 decreased release of CCK in irradiated rats compared to that in irradiated rats without vagotomy. However, i.p. administration of 10, 20 and 50 microg/kg of L-364,718 did not induce significant decreases in release of CCK in the hypothalamus of vagotomized and irradiated animals compared to those in rats that were vagotomized and irradiated but not treated with L-364,718. These results demonstrate that radiation increases the release of CCK in the hypothalamus, and that this effect is inhibited by vagotomy and the administration of a CCK-A receptor antagonist. A CCK-A receptor antagonist may be used to mitigate a radiation-induced deficit in food intake.
本研究旨在确定大鼠食物摄入量减少背后的机制。对以下几种情况下下丘脑内氯化钾刺激的胆囊收缩素(CCK)释放进行了测量:(a)γ射线照射(60Co)后;(b)使用CCK-A和CCK-B拮抗剂L-364,718和L-365,260治疗,包括有或无辐射的情况;(c)双侧腹部迷走神经切断术后;(d)迷走神经切断术联合或不联合辐射以及联合或不联合L-364,718。通过放射免疫分析法测量下丘脑灌流液中CCK的浓度。大鼠暴露于1、3、5和10 Gy(1 Gy/分钟)剂量的辐射后,下丘脑内CCK的释放以剂量依赖的方式增加。选择5 Gy剂量用于进一步研究。腹腔注射10、20和50 μg/kg的L-364,718对假照射动物的CCK释放未引起显著变化。然而,该药物以剂量依赖的方式降低了辐射诱导的CCK释放。与L-364,718相反,20 - 50 μg/kg的L-365,260降低了假照射动物下丘脑内CCK的释放,但未降低辐射暴露诱导的CCK释放。与假照射对照组相比,迷走神经切断术使CCK释放减少不显著。然而,与未行迷走神经切断术的照射大鼠相比,迷走神经切断术降低了照射大鼠的CCK释放。与未行迷走神经切断术的照射大鼠相比,迷走神经切断术联合腹腔注射10、20和50 μg/kg的L-364,718降低了照射大鼠的CCK释放。然而,与行迷走神经切断术并接受照射但未用L-364,718治疗的大鼠相比,腹腔注射10、20和50 μg/kg的L-364,718对行迷走神经切断术并接受照射动物下丘脑内CCK的释放未引起显著降低。这些结果表明,辐射增加了下丘脑内CCK的释放,且这种效应可被迷走神经切断术和CCK-A受体拮抗剂的给药所抑制。CCK-A受体拮抗剂可用于减轻辐射诱导的食物摄入量不足。