Key result
Superfusion of low-dose endothelin-3 with L-NMMA elicited arteriolar vasoconstriction that was suppressed by L-arginine, suggesting recovery of arteriolar diameter is mediated by nitric oxide.
Nitric oxide mediates the early-phase recovery of arteriolar diameter following endothelin-3-induced vasoconstriction in rat mesenteric microvessels.
May inform microvascular tone mechanisms in animals; leaves open translation to human endothelin-related vasospasm.
In order to clarify whether the vasoactive effects of endothelin-3 (ET-3) on microvessels are associated with the endothelium-derived relaxing factor (EDRF) in vivo, the authors examined the effects of L-NG-monomethyl arginine (L-NMMA), an analog of L-arginine, on low-dose ET-3 induced hemodynamic changes in the mesenteric microcirculation of male Wistar rats. The intravital observation revealed that ET-3 100 pM induced a remarkable and periodic vasoconstriction in arterioles, and the constriction was sustained for approximately fifteen minutes. No remarkable change was observed in the microvessels after the superfusion of 1 pM ET-3. Superfusion of 1 pM ET-3 with 100 microM L-NMMA elicited the vasoconstriction in arterioles, and the arteriolar diameter recovered to the control level within ten minutes in spite of continuing the superfusion. The vasoconstriction induced by low-dose ET-3 with L-NMMA was suppressed by the additional superfusion of 200 microM L-arginine. The present study suggests that the recovery of arteriolar diameter after the ET-3-induced constriction may be mediated by nitric oxide at least in the early phase.
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Kurose et al. (1993) studied this question. Endothelin-3 (ET-3) with L-NMMA vs. Baseline / 1 pM ET-3 alone was evaluated on Hemodynamic changes and vasoconstriction in arterioles. Superfusion of low-dose endothelin-3 with L-NMMA elicited arteriolar vasoconstriction that was suppressed by L-arginine, suggesting recovery of arteriolar diameter is mediated by nitric oxide.
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