S I Myers1, R Hernandez, A Castaneda. 1. Department of Surgery, University of Texas Southwestern Medical School, Dallas, Texas 75235, USA.
Abstract
BACKGROUND: This study examines the hypothesis that oxygen radicals down-regulate renal nitric oxide synthesis and contribute to renal vasoconstriction after hemorrhage/reperfusion injury. METHODS: Arterial pressure and renal artery blood flow were measured in anesthetized rats subjected to sham or hemorrhage (30 mm Hg for 30 minutes) followed by blood reperfusion without or with superoxide dismutase, an oxygen radical scavenger. Animals were sequentially injected with 10 mg/kg NG-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, and 200 mg/kg and 400 mg/kg L-arginine, a nitric oxide precursor. RESULTS: The L-NAME treatment increased arterial pressure and decreased renal artery blood flow whereas L-arginine decreased arterial pressure and decreased renal blood flow in the sham animals. Hemorrhage/reperfusion injury attenuated the pressure and renal blood flow changes following L-NAME and L-arginine treatment, which was reversed by superoxide dismutase. CONCLUSIONS: These data suggest that oxygen radicals contribute to the regulation of renal nitric oxide synthesis, contributing to renal artery vasoconstriction following hemorrhage/reperfusion injury.
BACKGROUND: This study examines the hypothesis that oxygen radicals down-regulate renal nitric oxide synthesis and contribute to renal vasoconstriction after hemorrhage/reperfusion injury. METHODS: Arterial pressure and renal artery blood flow were measured in anesthetized rats subjected to sham or hemorrhage (30 mm Hg for 30 minutes) followed by blood reperfusion without or with superoxide dismutase, an oxygen radical scavenger. Animals were sequentially injected with 10 mg/kg NG-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, and 200 mg/kg and 400 mg/kg L-arginine, a nitric oxide precursor. RESULTS: The L-NAME treatment increased arterial pressure and decreased renal artery blood flow whereas L-arginine decreased arterial pressure and decreased renal blood flow in the sham animals. Hemorrhage/reperfusion injury attenuated the pressure and renal blood flow changes following L-NAME and L-arginine treatment, which was reversed by superoxide dismutase. CONCLUSIONS: These data suggest that oxygen radicals contribute to the regulation of renal nitric oxide synthesis, contributing to renal artery vasoconstriction following hemorrhage/reperfusion injury.
Authors: Mahmood Rasool; Muhammad Abdul Basit Ashraf; Arif Malik; Sulayman Waquar; Shahida Aziz Khan; Mahmood Husain Qazi; Waseem Ahmad; Muhammad Asif; Sami Ullah Khan; Ahmad Zaheer; Muther Mansoor Qaisrani; Abdul Rehman Khan; Aamir Iqbal; Amir Raza; Saima Iram; Kashif Kamran; Asim Iqbal; Mohammad Zahid Mustafa; Hani Choudhry; Mazin A Zamzami; Wesam H Abdulaal; Mohammad Sarwar Jamal Journal: PLoS One Date: 2017-02-08 Impact factor: 3.240