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Protective Role of Selective Nitric Oxide Synthase Inhibitor for Treatment of Decompensated Hemorrhagic Shock in Normotensive and Hypertensive Rats
Abstract
Introduction: Different vasoactive factors can modulate
cardiovascular adaptation to hemorrhagic shock including Nitric
Oxide (NO). In this study we investigated the effect of the NO
synthase inhibitor for treatment of decompensated hemorrhagic
shock in normotensive and hypertensive rats.
Methods: Twenty‑four male Wistar rats were divided into two
groups: The normotensive and hypertensive groups. Hypertension was induced by the DOCA‑Salt method for eight weeks. Then, the animals were given hemorrhagic shock by continuously withdrawing blood until the mean arterial pressure (MAP) reached to 40 mmHg. The animals were maintained in the shock state for 120 minutes. Subsequently, they were randomly assigned to L‑NAME‑treated and non‑treated groups and monitored for 60 minutes. The survival time was recorded. Blood samples were taken before and after the shock and 60 minutes after L‑NAME administration.
Results: Infusion of L‑NAME caused a significant increase in
MAP in normotensive animals, however, slightly increased MAP
in hypertensive animals. The heart rate did not significantly alter. Hemorrhage caused a marked increase in serum nitrite levels in both groups (P<0.05). L‑NAME treatment significantly reduced the serum nitrite concentration in the normotensive group (P<0.05), without any change in the hypertensive group. All animals who received L‑NAME treatment survived at the end of experiment. Fifty percent of the hypertensive animals died four hours after the experiment. The 72‑hour survival rate was similar in the L‑NAME treated groups.
Conclusion: L‑NAME infusion during decompensated hemorrhagic shock plays a protective role in the improvement of hemodynamic responses and short‑term survival rate in
normotensive animals.
Keywords: Hypertension, hemorrhagic shock, nitric oxide
cardiovascular adaptation to hemorrhagic shock including Nitric
Oxide (NO). In this study we investigated the effect of the NO
synthase inhibitor for treatment of decompensated hemorrhagic
shock in normotensive and hypertensive rats.
Methods: Twenty‑four male Wistar rats were divided into two
groups: The normotensive and hypertensive groups. Hypertension was induced by the DOCA‑Salt method for eight weeks. Then, the animals were given hemorrhagic shock by continuously withdrawing blood until the mean arterial pressure (MAP) reached to 40 mmHg. The animals were maintained in the shock state for 120 minutes. Subsequently, they were randomly assigned to L‑NAME‑treated and non‑treated groups and monitored for 60 minutes. The survival time was recorded. Blood samples were taken before and after the shock and 60 minutes after L‑NAME administration.
Results: Infusion of L‑NAME caused a significant increase in
MAP in normotensive animals, however, slightly increased MAP
in hypertensive animals. The heart rate did not significantly alter. Hemorrhage caused a marked increase in serum nitrite levels in both groups (P<0.05). L‑NAME treatment significantly reduced the serum nitrite concentration in the normotensive group (P<0.05), without any change in the hypertensive group. All animals who received L‑NAME treatment survived at the end of experiment. Fifty percent of the hypertensive animals died four hours after the experiment. The 72‑hour survival rate was similar in the L‑NAME treated groups.
Conclusion: L‑NAME infusion during decompensated hemorrhagic shock plays a protective role in the improvement of hemodynamic responses and short‑term survival rate in
normotensive animals.
Keywords: Hypertension, hemorrhagic shock, nitric oxide