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Renal and hepatic family 3A cytochromes P450 (CYP3a) in spontaneously hypertensive rats

1995; Elsevier BV; Volume: 50; Issue: 1 Linguagem: Inglês

10.1016/0006-2952(95)00110-l

1873-2968

Sidhartha S. Ghosh, Ashish K. Basu, Shobha Ghosh, Rodney D. Hagley, Lora B. Kramer, John D. Schuetz, William Grogan, Philip S. Guzelian, Charles O. Watlington,

Eicosanoids and Hypertension Pharmacology

Troleandomycin (TAO), a selective family 3A cytochromes P450 (CYP3A) inhibitor, decreases enhanced in vivo corticosterone 6β-hydroxylation and blood pressure in spontaneously hypertensive rats (SHR). Corticosterone 6β-hydroxylation was measured in liver and kidney microsomes, to determine ontogeny and the effect of TAO on CYP3A activity at the organ level. SHR kidney CYP3A activity increased from 4 to 8 weeks, stabilized at 11 and 16 weeks, and was much higher than in control (Wistar-Kyoto, WKY) rats at all ages. Hepatic activity showed less consistency in strain difference. TAO produced a relatively large decrease in renal CYP3A activity compared with liver. Although renal CYP3A mRNA was not present in sufficient quantity for detection by northern blot analysis of total RNA, its presence was demonstrated in SHR by reverse transcriptase-polymerase chain reaction amplification. Correlations between renal CYP3A activity and systolic blood pressure in SHR and WKY rats with variations in age, strain and drug treatment are consistent with the role of the enzyme in the pathogenesis of blood pressure elevation in SHR.