R. Babbedge et al., BRADYKININ DEPOLARIZES THE RAT ISOLATED SUPERIOR CERVICAL-GANGLION VIA B-2 RECEPTOR ACTIVATION, Neuroscience letters, 193(3), 1995, pp. 161-164
Experiments were undertaken to characterise the action of kinins on sy
mpathetic neurones of the rat superior cervical ganglion (SCG) by use
of in vitro grease-gap, extracellular recording techniques in conjunct
ion with selective agonists and antagonists for B-1 and B-2 bradykinin
(BK) receptors. Superfusion of BK (10 nM to 10 mu M) to the ganglion
produced a concentration-related depolarisation (pD(2) = 7.02 +/- 0.04
, n = 7) which was inhibited by the selective B-2 antagonist HOE 140 (
10-100 nM), but not by the B-1 antagonist Leu(8)desArg(9) BK (1 mu M),
indomethacin (7 mu M) or the nitric oxide synthase inhibitor L-N-G-ni
troarginine methyl ester (300 mu M). DesArg(9)BK (10 nM to 10 mu M) ha
d no effect on membrane potential. Pre-treatment of animals with intra
venous bacterial lipolysaccharide (LPS, 3 mg kg(-1)) failed to induce
B-1 receptor-mediated depolarisations of SCG neurones, or change respo
nses to BK (P > 0.05, n = 4). These experiments highlight and characte
rise the action of BK as a neuromodulator of sympathetic neurones via
B-2 receptor activation.