Carr K D, Simon E J
Life Sci. 1983;33 Suppl 1:563-6. doi: 10.1016/0024-3205(83)90565-9.
We have previously shown that feeding induced by electrical stimulation in the lateral hypothalamus of rats is inhibited by naloxone but not its quaternary analogue. In the present study, effects of morphine and loperamide -an opiate that does not pass the blood-brain barrier- were examined. Loperamide inhibited stimulation-induced feeding; reversal of this effect by quaternary naloxone confirmed the peripheral site of action. A low dose of morphine (1.25 mg/kg) facilitated feeding but higher doses were inhibitory. An inhibitory dose of morphine became facilitory, however, when preceded by quaternary naloxone. It therefore appears that central opioid activity promotes ingestive behavior while peripheral activity inhibits ingestion. To evaluate the function served by the central facilitory process, we exploited the relation that exists between feeding and self-stimulation elicited through a common electrode. It was found that potentiation of self-stimulation by food deprivation is blocked by naloxone. It is concluded that endogenous opioid activity may promote feeding by enhancing the reward value of food as a function of hunger.
我们之前已经表明,电刺激大鼠下丘脑外侧诱发的进食行为可被纳洛酮抑制,但不能被其四元类似物抑制。在本研究中,我们检测了吗啡和洛哌丁胺(一种不能透过血脑屏障的阿片类药物)的作用。洛哌丁胺抑制刺激诱发的进食;四元纳洛酮对这种作用的逆转证实了其作用部位在外周。低剂量的吗啡(1.25毫克/千克)促进进食,但高剂量则起抑制作用。然而,当在四元纳洛酮之前给予抑制剂量的吗啡时,该抑制剂量的吗啡却变成了促进作用。因此,似乎中枢阿片类活性促进摄食行为,而外周活性则抑制摄食。为了评估中枢促进过程所起的作用,我们利用了通过同一电极诱发的进食和自我刺激之间存在的关系。研究发现,食物剥夺引起的自我刺激增强可被纳洛酮阻断。我们得出结论,内源性阿片类活性可能通过增强食物作为饥饿函数的奖励价值来促进进食。