Enters E K, Spear L P
Department of Psychology, State University of New York, Binghamton 13901.
Psychopharmacology (Berl). 1988;96(2):161-8. doi: 10.1007/BF00177555.
The effects of various doses of the serotonergic agonist quipazine and antagonist methysergide on mouthing behavior under both low and high baseline mouthing conditions (i.e., in the absence and presence of milk, respectively) was examined in deprived and non-deprived rat pups at 3-4, 10-11 and 16-17 days postnatally. Quipazine was observed to induce an increase in mouthing in neonatal rat pups, both increases and decreases in mouthing at 10-11 days of age, while exerting a depressant effect on mouthing at 16-17 days postnatally. Methysergide conversely depressed mouthing at the two earlier testing periods, while having little effect on this behavior at 16-17 days postnatally. These ontogenetic transitions in the influence of serotonergic manipulations on mouthing are reminiscent of the ontogenetic reversal previously reported to occur in the influence of serotonergic manipulations on suckling (Ristine and Spear 1984). These developmental discontinuities in the serotonergic system may provide an excellent model system for the investigation of neural mechanisms mediating age-specific behaviors and their ontogenetic decline.
在出生后3 - 4天、10 - 11天和16 - 17天的剥夺和未剥夺的幼鼠中,研究了不同剂量的血清素能激动剂喹哌嗪和拮抗剂甲基麦角新碱在低基线和高基线吮乳条件下(即分别在无奶和有奶的情况下)对吮乳行为的影响。观察到喹哌嗪可诱导新生幼鼠吮乳增加,在10 - 11日龄时吮乳有增有减,而在出生后16 - 17天对吮乳有抑制作用。相反,甲基麦角新碱在较早的两个测试阶段抑制吮乳,而在出生后16 - 17天对这种行为影响很小。血清素能操作对吮乳影响的这些个体发生转变让人想起先前报道的血清素能操作对哺乳影响中发生的个体发生逆转(里斯汀和斯皮尔,1984年)。血清素能系统中的这些发育不连续性可能为研究介导特定年龄行为及其个体发生衰退的神经机制提供一个极好的模型系统。