Dorsal medullary brain slices containing primarily the nucleus tractus solitarius (NTS) were obtained from normal or 40- to 50-day streptozotocin-diabetic rats and employed for superfusion studies of evoked transmitter release. Electrically stimulated (25 ma, 2-ms pulses, 3 Hz, 1 min) release of[H-3]norepinephrine([H-3]NE)or[H-3]5-hydroxytryptamine ([H-3]5-HT) from 400-mu m NTS slices stimulated at 75 min (S-1) and 130 min (S-2) resulted in S-2/S-1 release ratios that were not different between normal controls or diabetic control groups. Perfusion of normal [H-3]NE-loaded slices with 0.1 mu mol/l clonidine reduced the S-2/S-1 ratio by 23% (p < 0.05) which was uniform in the caudal, subpostremal, and intermediate segment levels of the NTS. In diabetic NTS slices, the S-2/S-1 ratio was significantly less reduced by clonidine in both the subpostremal (-3%) and intermediate (-11%) slice regions. Blockade of a(2)-adrenoceptors with yohimibine (0.1 mu mol/l) enhanced (p < 0.05) [H-3]NE release (S-2/S-1 ratios) in slices from both normal and diabetic rats, Perfusion of [H-3]NE-loaded slices with 5 mU/ml insulin did not affect St release. Evoked S-2/S-1 release ratios from NTS slices loaded with [H-3]5-HT did not differ between normal control and diabetic control groups. Clonidine (0,1 mu mol/l) reduced Sz-evoked release in both normal (-30%) and diabetic (-44%) slices, but the groups were not different from each other. Superfusion with 5 mU/ml insulin did not alter S-2/S-1 ratios in normal [H-3]5-HT loaded slices? but did increase the diabetic NTS slice S-2/S-1 I ratio to 1,40 +/- 0.06 (p < 0.01), In summary, it appears that alpha(2)-adrenoceptor-mediated inhibition of [H-3]NE release in the NTS was selectively attenuated in a regionally specific manner in diabetic animals, Release inhibition may be associated with receptor downregulation in NTS regions associated with cardiovascular reflex transmission. Insulin superfusion augmented [H-3]5-HT release in the diabetic NTS slices, possibly through increased transmitter synthesis or improved synaptic release.