Key result
Intravenous and intracerebroventricular injection of agmatine prevented the development of ischemia/reperfusion-induced renal injury in rats by suppressing enhanced renal sympathetic nerve activity.
Why the study?
Does agmatine prevent ischemia/reperfusion-induced renal injury in rats?
Does agmatine prevent ischemia/reperfusion-induced renal injury in rats?
Agmatine protects against ischemia/reperfusion-induced acute renal failure in rats by suppressing sympathetic nerve activity and norepinephrine overflow.
Cautions against clinical use; leaves open translation of agmatine’s sympathetic effects from rat renal ischemia/reperfusion models.
Enhanced renal sympathetic nerve activity (RSNA) during ischemic period and the renal venous norepinephrine (NE) overflow after reperfusion play important roles in the development of ischemic/reperfusion (I/R)-induced acute renal failure (ARF) in rats. This study evaluated whether agmatine, which is known to reduce sympathetic nerve activity and NE overflow by electrical stimulation, would prevent the I/R-induced renal dysfunction. Ischemic ARF was induced by clamping the left renal artery and vein for 45 minutes followed by reperfusion 2 weeks after the contralateral nephrectomy. Intravenous (IV) injection of agmatine (100 and 300 micromol/kg) to ischemic ARF rats dose-dependently suppressed the enhanced RSNA and attenuated the I/R-induced renal dysfunction and histological damage. Intracerebroventricular (ICV) injection of agmatine (600 nmol/kg) to ischemic ARF rats suppressed the enhanced RSNA during the ischemic period and attenuated the I/R-induced renal injury. Furthermore, both IV and ICV injection of agmatine significantly suppressed the renal venous NE overflow after the reperfusion. These results indicate that agmatine prevents the development of I/R-induced renal injury, and the effect is accompanied by suppression of the enhanced RSNA during ischemic period and NE overflow from renal sympathetic nerve endings.
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Sugiura et al. (2008) studied Ischemia/reperfusion-induced acute renal failure. Agmatine was evaluated on Renal dysfunction, histological damage, renal sympathetic nerve activity, and renal venous norepinephrine overflow. Intravenous and intracerebroventricular injection of agmatine prevented the development of ischemia/reperfusion-induced renal injury in rats by suppressing enhanced renal sympathetic nerve activity.
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