Role of Phospholipases A in Vascular Relaxation and Sympatholytic Effects of Five Australian Brown Snake, spp., Venoms in Rat Isolated Tissues.

Human envenoming by Australian brown snakes ( spp.) may result in potentially life-threatening hypotension and subsequent cardiovascular collapse. There have been relatively few studies of the cardiovascular and sympathetic effects of spp. venoms. In this study, we have examined the effects of venom from five brown snake species-, and -on cardiac inotropic and chronotropic responses, vascular tone, and sympathetic nerve-induced vascular contractions in rat isolated tissues. The role of phospholipases A (PLAs) in venom-induced effects was assessed with the sPLA inhibitor varespladib. In rat isolated left and right atria, there were no physiologically relevant effects of venoms (0.1-30 µg/ml) on left atrial force of contraction (inotropy) or right atrial rate (chronotropy). In contrast, in isolated small mesenteric arteries precontracted with a thromboxane mimetic, each of the five brown snake venoms (at 30 µg/ml) caused marked vasorelaxation (-60 to -90% of contractile tone). Pretreatment with varespladib (1 µM) significantly inhibited the vasorelaxation caused by , and venoms. Electrically induced sympathetic nerve-mediated contractions of mesenteric arteries were significantly attenuated by only , and venoms (30 µg/ml) and these sympatholytic effects were inhibited by varespladib (1 µM). Based on their inhibition with the sPLA inhibitor varespladib, we conclude that PLA toxins in , , and venoms are involved in brown snake venom-induced vasorelaxation and the sympatholytic effects of , and venoms. Our study supports the promising potential role of varespladib as an initial (pre-referral) and/or adjunct (in combination with antivenom) therapeutic agent for brown snake envenoming.