Normal erythrocyte calpain I activity on membrane proteins under near-physiological conditions in patients with essential hypertension

Sao Paulo Medical Journal

Tereza Maria Dantas De Medeiros²  Katia Coelho Ortega¹  Décio Mion Júnior¹  Kimiyo Nonoyama¹  Orlando Cesar De Oliveira Barretto¹ 

[1],Universidade Federal do Rio Grande do Norte Clinical Chemistry and Toxicology Department Natal,Brazil

关键词: Calpain I;    Calpastatin;    Red cell membrane proteins;    Band 2.1;    Band 4.1;    Essential hypertension;    Calpaina I;    Calpastatina;    Proteinas da membrana eritrocitaria;    Banda 2.1;    Banda 4.1;    Hipertensão essencial;   

DOI  :  10.1590/S1516-31802002000100002

来源: SciELO

【 摘 要 】

CONTEXT: It has been reported that the equilibrium between the erythrocyte protease calpain I and its physiological inhibitor calpastatin is disrupted in patients with essential hypertension. OBJECTIVE: To investigate the activity of non-purified calpain I in hemolysates against the erythrocytic membrane proteins, rather than against other substrates. DESIGN: Evaluation of calpain I red cell activity upon its own physiological substrates in hypertensive patients, in a near-physiological environment. SETTING: LIM-23 and LIM-40 of Hospital das Clinicas of the Faculty of Medicine of USP. SAMPLE: Patients with moderate primary hypertension over 21 years of age who were given amlodipine (n:10) and captopril (n:10) for 8 weeks, plus normal controls (n:10). MAIN MEASUREMENTS: Red cell membrane proteins were incubated with and without protease inhibitors and with and without calcium chloride and underwent polyacrylamide gel electrophoresis. RESULTS: Digestion of bands 2.1 and 4.1 was observed, indicating calpain I acitivity. No statistical differences regarding bands 2.1 and 4.1 were observed before treatment, between the controls and the hypertensive patients, either in ghosts prepared without calcium or with increasing concentrations of calcium. Nor were statistical differences observed after treatment, between the controls and the patients treated with amlodipine and captopril, or between the patients before and after treatment with both drugs. CONCLUSION: The final activity of non-purified calpain I upon its own physiological substrate, which was the approach utilized in this study, may more adequately reflect what happens in red cells. Under such conditions no imbalance favoring calpain I activity increase was observed. The protective factor provided by calpastatin against calpain I activity may diminish under hypertension.

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