OBJECTIVE: To determine whether alterations in cardiac G-protein number or function, or both, are involved in the desensitization of adenylate cyclase responsiveness in the hypertensive state. DESIGN: Quantitation of G-protein subunits in myocardial membranes from four different rat models of hypertension in comparison with respective normotensive rats. METHODS: We compared male and female adult spontaneously hypertensive rats (SHR) with age- and sex-matched Wistar-Kyoto (WKY) rats, rats from the highest-pressure quartile from an F2 generation of WKY x SHR hybrids with those from the lowest-pressure quartile, and one-kidney, one clip renal hypertensive with sham-operated rats. The function of Gs alpha was quantitated by reconstitution of cardiac cholate extracts into cyc- cell membranes with subsequent measurement of NaF-stimulated adenylate cyclase activity. The amounts of immunodetectable Gs alpha, Gi alpha, Gq alpha and G beta were determined from quantitative Western blotting experiments with [125I]-protein A detection. RESULTS: None of the parameters investigated differed significantly between hypertensive and normotensive rats in any of the models investigated. CONCLUSION: We conclude that major quantitative alterations in cardiac Gs, Gi or Gq are not a general feature of the hypertensive state.
OBJECTIVE: To determine whether alterations in cardiac G-protein number or function, or both, are involved in the desensitization of adenylate cyclase responsiveness in the hypertensive state. DESIGN: Quantitation of G-protein subunits in myocardial membranes from four different rat models of hypertension in comparison with respective normotensive rats. METHODS: We compared male and female adult spontaneously hypertensiverats (SHR) with age- and sex-matched Wistar-Kyoto (WKY) rats, rats from the highest-pressure quartile from an F2 generation of WKY x SHR hybrids with those from the lowest-pressure quartile, and one-kidney, one clip renal hypertensive with sham-operated rats. The function of Gs alpha was quantitated by reconstitution of cardiac cholate extracts into cyc- cell membranes with subsequent measurement of NaF-stimulated adenylate cyclase activity. The amounts of immunodetectable Gs alpha, Gi alpha, Gq alpha and G beta were determined from quantitative Western blotting experiments with [125I]-protein A detection. RESULTS: None of the parameters investigated differed significantly between hypertensive and normotensive rats in any of the models investigated. CONCLUSION: We conclude that major quantitative alterations in cardiac Gs, Gi or Gq are not a general feature of the hypertensive state.