Accession Number : ADA628168


Title :   Hemorrhagic Shock-Induced Vascular Hyporeactivity in the Rat: Relationship to Gene Expression of Nitric Oxide Synthase, Endothelin-1, and Select Cytokines in Corresponding Organs


Descriptive Note : Journal article


Corporate Author : ARMY INST OF SURGICAL RESEARCH FORT SAM HOUSTON TX


Personal Author(s) : Liu, Liang-Ming ; Dubick, Michael A


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/a628168.pdf


Report Date : Jan 2005


Pagination or Media Count : 10


Abstract : Background. Our previous work observed that vascular hyporeactivity to norepinephrine (NE) developed after hemorrhage and the response was not the same in the 4 arteries examined. To evaluate possible mechanisms involved, the present study investigated the gene expression of iNOS, eNOS, IL-1 Beta , IL-6, TNF-alpha , and endothelin-1 in the corresponding organs, and the roles of nitric oxide (NO) and endothelin (ET). Materials and methods. LAnesthetized rats (n = 7/time point/group) were hemorrhaged to a mean arterial pressure of 50 mmHg for 60 min. The vascular reactivity of the superior mesenteric (SMA), celiac (CA), left renal (LRA), and left femoral arteries (LFA) to NE was measured at baseline, at the end of the hypotensive period (E), and at 1, 2, an d 4 h later in the three groups (hemorrhage, hemorrhage NG-nitro-L-arginine methyl ester (L -NAME), an NO synthase inhibitor, or hemorrhage PD142893, an ET receptor antagonist). Gene expression inileum, left kidney, liver, and skeletal muscle was determined by quantitative RT-PCR at these times. Results. Vascular reactivity of SMA, CA, LRA, and LFA to NE decreased as much as 98% over 4 h compared with baseline. This loss of responsiveness in CA and LFA was more severe than in SMA and LRA. Gene expression of iNOS, eNOS, IL-1 beta, IL-6, TNF-alpha, and endothelin-1 in the corresponding organs of select vasculatures increased markedly over baseline levels and the fold increase in mRNA levels of these enzymes and mediators in liver and skeletal muscle was higher than in ileum and left kidney. For example, at 4 h, iNOS expression was over 16-fold higher than baseline in liver and skeletal muscle, but 5- and 7-fold higher in ileum and kidney, respectively. L -NAME or PD142893 partially attenuated the decreased vascular reactivity induced by hemorrhagic shock and attenuated the changes in gene expression observed.


Descriptors :   *CYTOKINES , *GENE EXPRESSION , *HEMORRHAGIC SHOCK , *ORGANS(ANATOMY) , *RATS , AMINO ACIDS , BLOOD PRESSURE , CARDIOVASCULAR SYSTEM , ENZYMES , ESTERS , FEMORAL ARTERIES , ILEUM , KIDNEYS , LIVER , METHYL RADICALS , MUSCULOSKELETAL SYSTEM , NITRIC OXIDE , OXIDES , PERITONEUM , RECEPTOR SITES(PHYSIOLOGY) , RESISTANCE(BIOLOGY) , RESPONSE(BIOLOGY) , SYNTHASES


Subject Categories : Biochemistry
      Genetic Engineering and Molecular Biology
      Medicine and Medical Research


Distribution Statement : APPROVED FOR PUBLIC RELEASE