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(Hypertension. 2009;54:210.)
© 2009 American Heart Association, Inc.
Brief Reviews |
From the Instituto de Bioquímica Médica (J.M.A.D., M.A.M.C.) and Instituto de Biofísica Carlos Chagas Filho (A.G.L., M.A.M.C.), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Correspondence to Márcia A.M. Capella, Instituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, CCS-Bloco G, 21949-900 Rio de Janeiro, RJ, Brazil. E-mail mcapella@biof.ufrj.br
An extract of the first 250 words of the full text is provided, because this article has no abstract. |
| Introduction |
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54% of stroke, 47% of ischemic heart disease, 75% of hypertensive disease, and 25% of other cardiovascular disease worldwide can be attributable to high blood pressure.2 Altered levels of angiotensin and aldosterone are common findings in hypertension. Aldosterone has been shown to play an important role in the pathophysiology of numerous cardiovascular disorders, including heart failure and hypertension,3 and the renin-angiotensin-aldosterone system is currently an important target for 5 antihypertensive drug classes: β-blockers, renin inhibitors, angiotensin-conversion enzyme inhibitors, angiotensin receptor blockers, and aldosterone antagonists.4
In the last few years, increasing evidence has pointed to an involvement of multidrug resistance (MDR)-related proteins with hypertension. Both ABCB1 (P-glycoprotein) and ABCC1 (MDR-associated protein 1), the 2 main proteins first described in multidrug-resistant tumors, are known to physiologically transport several endobiotics, including hormones.5,6 Moreover, ABCB1 and ABCG2 (the third protein related to MDR), seem to also be related to the secretion of several drugs to urine, including some antihypertensives.7,8 This review summarizes the recent findings regarding the relationship between MDR-related proteins and hypertension.
| ABC Superfamily and MDR in Cancer |
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1 of 3 proteins belonging to
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