Hayes Matthew R, Moore Rachael L, Shah Samit M, Covasa Mihai
Dept. of Nutritional Sciences, College of Health and Human Development, The Pennsylvania State Univ., 126 South Henderson, University Park, PA 16802, USA.
Am J Physiol Regul Integr Comp Physiol. 2004 Oct;287(4):R817-23. doi: 10.1152/ajpregu.00295.2004. Epub 2004 Jun 10.
Serotonin type 3 (5-HT(3)) receptors have been shown to participate in the negative-feedback control of food intake. We previously reported that cholecystokinin (CCK)-induced suppression of food intake is partly mediated through 5-HT(3) receptors when rats were tested on a preferred liquid diet, but whether such an effect occurs when they are tested on a solid maintenance diet is unknown. In the present study, we examined the effects of ondansetron, a selective 5-HT(3) antagonist, on CCK-induced suppression of solid chow intake. Intraperitoneal administration of ondansetron significantly attenuated 30- and 60-min CCK-induced reduction of food intake, with suppression being completely reversed by 120 min. It is not known whether 5-HT(3) receptors directly mediate CCK-induced satiation or whether their participation depends on CCK acting as part of a feedback cascade to inhibit ongoing intake. Because CCK-induced inhibition of sham feeding does not depend on additive gastric/postgastric-feedback signals, we examined the ability of ondansetron to reverse CCK-induced satiation in sham-feeding rats. Ondansetron did not attenuate reduction of sham feeding by CCK, suggesting that ondansetron does not directly antagonize CCK-satiation signals. CCK suppresses real feeding through a delay in gastric emptying. Ondansetron could attenuate CCK-induced reduction of food intake by reversing CCK-induced inhibition of gastric emptying. We found that blockade of 5-HT(3) receptors attenuates CCK-induced inhibition of gastric emptying of a solid meal, as well as saline and glucose loads. We conclude that 5-HT(3) receptors mediate CCK-induced satiation through indirect mechanisms as part of a feedback cascade involving inhibition of gastric emptying.
血清素3型(5-HT(3))受体已被证明参与食物摄入的负反馈控制。我们之前报道,当大鼠在偏好的流食饮食上进行测试时,胆囊收缩素(CCK)诱导的食物摄入抑制部分是通过5-HT(3)受体介导的,但当它们在固体维持饮食上进行测试时,这种效应是否发生尚不清楚。在本研究中,我们研究了选择性5-HT(3)拮抗剂昂丹司琼对CCK诱导的固体食物摄入量抑制的影响。腹腔注射昂丹司琼显著减弱了CCK诱导的30分钟和60分钟食物摄入量的减少,抑制作用在120分钟时完全逆转。尚不清楚5-HT(3)受体是直接介导CCK诱导的饱腹感,还是它们的参与依赖于CCK作为反馈级联的一部分来抑制正在进行的进食。由于CCK诱导的假饲抑制不依赖于附加的胃/胃后反馈信号,我们研究了昂丹司琼逆转CCK诱导的假饲大鼠饱腹感的能力。昂丹司琼没有减弱CCK对假饲的减少,这表明昂丹司琼不直接拮抗CCK饱腹感信号。CCK通过延迟胃排空来抑制实际进食。昂丹司琼可以通过逆转CCK诱导的胃排空抑制来减弱CCK诱导的食物摄入量减少。我们发现,阻断5-HT(3)受体会减弱CCK诱导的固体餐、生理盐水和葡萄糖负荷的胃排空抑制。我们得出结论,5-HT(3)受体通过间接机制介导CCK诱导的饱腹感,作为涉及抑制胃排空的反馈级联的一部分。