Hemodynamic effects of python neuropeptide gamma in the anesthetized python, Python regius.

Click for Abstract : The effects of python neuropeptide gamma (NP?) on hemodynamic parameters have been investigated in the anesthetized ball python (Python regius). Bolus intra-arterial injections of synthetic python NP? (1�300 pmol kg?1) produced a dose-dependent decrease in systemic arterial blood pressure (Psys) concomitant with increases in systemic vascular conductance (Gsys), total cardiac output and stroke volume, but only minor effects on heart rate. The peptide had no significant effect on pulmonary arterial blood pressure (Ppul) and caused only a small increase in pulmonary conductance (Gpul) at the highest dose. In the systemic circulation, the potency of the NK1 receptor-selective agonist [Sar9,Met(02)11)] substance P was >100-fold greater than the NK2 receptor-selective agonist [?Ala8] neurokinin A-(4�10)-peptide suggesting that the python cardiovascular system is associated with a receptor that resembles the mammalian NK1 receptor more closely than the NK2 receptor. Administration of the inhibitor of nitric oxide synthesis, L-nitro-arginine-methylester (L-NAME; 150 mg kg?1), resulted in a significant (P<0.05) increase in�Psys�as well as a decrease in�Gsys, but no effect on�Ppul�and�Gpul. Conversely, the nitric oxide donor, sodium nitroprusside (SNP; 60 ?g kg?1) produced a significant (P<0.05) decrease in�Psys�along with an increase in�Gsys�and pulmonary blood flow. However, neither L-NAME nor indomethacin (10 mg kg?1) reduced the cardiovascular responses to NP?. Thus, nitric oxide is involved in regulation of basal vascular tone in the python, but neither nitric oxide nor prostaglandins mediate the vasodilatory action of NP?.