https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 D. russelii venom mediates vasodilatation of resistance like arteries via activation of Kv and KCa channels https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:45245 Daboia russelii) venom causes a range of clinical effects in humans. Hypotension is an uncommon but severe complication of Russell’s viper envenoming. The mechanism(s) responsible for this effect are unclear. In this study, we examined the cardiovascular effects of Sri Lankan D. russelii venom in anaesthetised rats and in isolated mesenteric arteries. D. russelii venom (100 µg/kg, i.v.) caused a 45 ± 8% decrease in blood pressure within 10 min of administration in anaesthetised (100 µg/kg ketamine/xylazine 10:1 ratio, i.p.) rats. Venom (1 ng/mL–1 µg/mL) caused concentration-dependent relaxation (EC50 = 145.4 ± 63.6 ng/mL, Rmax = 92 ± 2%) in U46619 pre-contracted rat small mesenteric arteries mounted in a myograph. Vasorelaxant potency of venom was unchanged in the presence of the nitric oxide synthase inhibitor, L-NAME (100 µM), or removal of the endothelium. In the presence of high K+ (30 mM), the vasorelaxant response to venom was abolished. Similarly, blocking voltage-dependent (Kv: 4-aminopryidine; 1000 µM) and Ca2+-activated (KCa: tetraethylammonium (TEA; 1000 µM); SKCa: apamin (0.1 µM); IKCa: TRAM-34 (1 µM); BKCa; iberiotoxin (0.1 µM)) K+ channels markedly attenuated venom-induced relaxation. Responses were unchanged in the presence of the ATP-sensitive K+ channel blocker glibenclamide (10 µM), or H1 receptor antagonist, mepyramine (0.1 µM). Venom-induced vasorelaxtion was also markedly decreased in the presence of the transient receptor potential cation channel subfamily V member 4 (TRPV4) antagonist, RN-1734 (10 µM). In conclusion, D. russelii-venom-induced hypotension in rodents may be due to activation of Kv and KCa channels, leading to vasorelaxation predominantly via an endothelium-independent mechanism. Further investigation is required to identify the toxin(s) responsible for this effect.]]> Wed 26 Oct 2022 19:42:29 AEDT ]]> Post-stimulus potentiation of transmission in pelvic ganglia enhances sympathetic dilatation of guinea-pig uterine artery in vitro https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:1583 Wed 11 Apr 2018 12:16:23 AEST ]]> A Role for H2S in the microcirculation of newborns: the major metabolite of H2S (thiosulphate) is increased in preterm infants https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:16029 Wed 11 Apr 2018 10:10:44 AEST ]]> Low dose resveratrol improves cerebrovascular function in type 2 diabetes mellitus https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:28573 Thu 27 Jan 2022 15:55:26 AEDT ]]> Dynamic range of evoked cholinergic and non-cholinergic non-adrenergic vasodilatation in bronchoesphageal circulation in the awake dog https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:12782 Sat 24 Mar 2018 08:17:34 AEDT ]]> Modulation of baroreflex gain regulating coronary vasodilator responses by the central μ-opioid receptor agonist fentanyl https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:12783 Sat 24 Mar 2018 08:17:34 AEDT ]]>