Currie P J, Fletcher P J, Coscina D V
Section of Biopsychology, Clarke Institute of Psychiatry, Toronto, Ontario, Canada.
Am J Physiol. 1994 May;266(5 Pt 2):R1645-51. doi: 10.1152/ajpregu.1994.266.5.R1645.
The 5-hydroxytryptamine (5-HT)1A agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) has been shown to elicit dose-dependent feeding in satiated rats when injected into the midbrain raphe nuclei. Because the feeding-stimulatory effects of this compound are associated with reduced 5-HT release in forebrain, and because recent evidence suggests that medial hypothalamic norepinephrine (NE) and 5-HT may function antagonistically in the control of feeding, the present study sought to determine whether 8-OH-DPAT would enhance feeding induced by infusing NE into the medial hypothalamus. All experiments were conducted using ad libitum-fed adult male rats with two indwelling cannulas, one aimed at the paraventricular nucleus (PVN), the other at either the dorsal or median raphe. In the first series of experiments rats received a fixed dose of 8-OH-DPAT (0.8 nmol) microinjected into the dorsal or median raphe, as well as NE (0, 10, 20 nmol) administered into the PVN. In the second series, rats received varying doses of raphe 8-OH-DPAT (0, 0.4, 0.8 nmol) coinjected with a single dose of PVN NE (20 nmol). Results indicated that 8-OH-DPAT and NE both elicited reliable increases in 1-h food intake, although their effects did not interact. In the final series, rats were injected with subthreshold doses of both compounds. While combined injections of 8-OH-DPAT and NE modestly increased feeding compared with saline control, this increase was not significantly greater than intake found after injection of 8-OH-DPAT or NE alone.(ABSTRACT TRUNCATED AT 250 WORDS)
5-羟色胺(5-HT)1A激动剂8-羟基-2-(二正丙基氨基)四氢萘(8-OH-DPAT)已被证明,当注射到中脑缝际核时,能在饱足的大鼠中引发剂量依赖性进食。由于该化合物的进食刺激作用与前脑5-HT释放减少有关,且最近的证据表明内侧下丘脑去甲肾上腺素(NE)和5-HT在进食控制中可能起拮抗作用,因此本研究旨在确定8-OH-DPAT是否会增强通过向内侧下丘脑注入NE所诱导的进食。所有实验均使用随意进食的成年雄性大鼠进行,大鼠体内植入两根套管,一根对准室旁核(PVN),另一根对准背侧或中缝际。在第一组实验中,大鼠接受固定剂量(0.8 nmol)的8-OH-DPAT微量注射到背侧或中缝际,以及向PVN注入NE(0、10、20 nmol)。在第二组实验中,大鼠接受不同剂量的中缝际8-OH-DPAT(0、0.4、0.8 nmol)与单剂量的PVN NE(20 nmol)共同注射。结果表明,8-OH-DPAT和NE均能可靠地增加1小时食物摄入量,尽管它们的作用没有相互影响。在最后一组实验中,给大鼠注射两种化合物的阈下剂量。虽然与生理盐水对照组相比,8-OH-DPAT和NE联合注射适度增加了进食量,但这种增加并不显著大于单独注射8-OH-DPAT或NE后的摄入量。(摘要截短至250字)