Grooming reflexes are induced by frontal neocortical, pontile, or spinal lesions in dogs and cats. In intact cats, the combined treatments of adrenalectomy and para-chlorophenylalanine administration induce grooming reflexes. Two other ways of depleting serotonin (with 5,7-dihydroxytryptamine and raphe lesions) were combined with adrenalectomy in the present study as further tests that serotonin and glucocorticoid hormones are the critical factors in the induction of grooming reflexes. Because the deficit in serotonin is confined to the superior colhculi in cats with frontal and pontile lesions, 5,7-dihydroxytryptamine (5,7-DHT) was injected directly into the superior colhculi at eight sites, 2 ^g/site (1 ^1 at .5 /ul/min). Electrolytic dc lesions of the dorsal and superior central raphe nuclei were made in another group, and then both groups were adrenalectomized. There were three control groups (a) a group with vehicle injections in the superior colliculi and laporatomies, (b) a group with 5,7-DHT injections in the superior colliculi, and (c) a group with the raphe lesions. Large receptive fields for grooming reflexes occurred only in the groups with combined treatments. Thus the mechanism of induction of grooming reflexes by central nervous system lesions involves independent changes in a hormonal and a neurotransmitter system which combine to effect the change in beh?vior.
The present study was undertaken to evaluate the 24-hour periodicity in serum prolactin levels subsequent to transecting the ascending serotonergic system or ablating the suprachiasmatic nuclei (SCN) of adult (185 g) female rats. The ascending serotonergic system was transected at the level of the rostral mesencephalon using a 1.5 mm wide knife and the SCN was ablated with a modified Halász-Pupp knife. The effect of raphe transection (RT) or SCN ablation on the circadian rhythm in nonstress serum prolactin levels was assessed 45 days after surgery by measuring with radioimmunoassay the serum prolactin concentration in serial blood samples obtained from the tail vein of lightly restrained rats. Serum prolactin concentration in control and RT animals showed circadian periodicity; peak levels occurred during the midafternoon, 4 h prior to the dark phase of the lighting regime (lights on at 4 a.m., off at 6 p.m.). The amplitude of the fluctuations of both groups varied markedly and were related to the estrous cycle. However, RT animals showed a reduced amplitude in the rhythm. In controls peak prolactin levels on days of proestrus and estrus were 15–20 times higher than on days of diestrus. In contrast, serum prolactin levels in SCN-ablated rats did not vary with a circadian periodicity but rather showed random, low amplitude fluctuations. Reproductive cyclicity was also abolished by SCN ablation, i.e., SCN-ablated rats presented persistent vaginal cornification. These data indicate that circadian periodicity in serum prolactin levels is not compromised by sectioning the ascending serotonergic fibers but is abolished after ablating the SCN.
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