The purposes of the present study were to: (1) characterize the GABAer
gic input to vasodepressor neurons in the caudal ventrolateral medulla
of the cat, and (2) define more precisely the anatomical localization
of these neurons in this species. This was done by microinjecting GAB
A receptor antagonists and agonists, and a negative allosteric modulat
or of the GABA receptor, namely, ethyl-beta-carboline-3-carboxylate, i
nto the caudal ventrolateral medulla of alpha-chloralose-anesthetized
animals while monitoring arterial blood pressure and heart rate. Local
ization studies were performed relating injection sites in the caudal
ventrolateral medulla where cardiovascular responses were elicited, to
neurons exhibiting immunoreactivity to tyrosine hydroxylase (TH) and
phenethyl-N-methyl-transferase (PNMT). Microinjection of 1 and 10 ng o
f bicuculline into the caudal ventrolateral medulla produced decreases
in mean blood pressure and heart rate of -34 +/- 6.4 and -49 +/- 9.2
mmHg, and -22 +/- 3.3 and -35 +/- 8.2 beats/min, respectively. Hypoten
sion and bradycardia were also observed with picrotoxin microinjection
(120 ng). Microinjection of muscimol (100-200 ng) and GABA(12 mu g) i
nto the caudal ventrolateral medulla counteracted the cardiovascular e
ffects of the GABA antagonists. Microinjection of muscimol per se had
no effect on mean blood pressure and heart rate. Microinjection of eth
yl-beta-carboline-3-carboxylate also decreased mean blood pressure (-3
9 +/- 7.0 mmHg). The location of the micropipette tip after bicucullin
e microinjection in relation to TH and PNMT immunoreactive cells was a
s follows: (1) TH-immunoreactive cells of the A1 cell group were visib
le in the same relative location as the micropipette tip, and (2) no P
NMT-positive cells were noted at the sites where bicuculline elicited
hypotension. These results indicate that there is a tonic GABAergic in
put to neurons in the caudal ventrolateral medulla. The location of th
ese neurons overlaps with the A1 cells.