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1.
Am J Hypertens ; 12(8 Pt 1): 784-9, 1999 Aug.
Article in English | MEDLINE | ID: mdl-10480471

ABSTRACT

The ability of angiotensin converting enzyme (ACE) inhibitors to lower blood pressure may in part be due to the formation of vasodilatory prostaglandins. Inhibition of prostaglandin synthesis with aspirin may therefore theoretically attenuate the antihypertensive effect of ACE inhibitors. This trial studied the interaction between aspirin (ASA) and enalapril, an ACE inhibitor, and ASA and losartan, an angiotensin subtype 1 receptor antagonist. Seventeen essential hypertensive patients were studied, maintained on a stable dose of either enalapril (n = 7) or losartan (n = 10) monotherapy for > or =12 weeks before and throughout the study. Each patient received a 2-week course of placebo, 81 mg/day ASA, and 325 mg/day ASA, each treatment separated by a 2-week washout period. Blood pressure (BP) and serum thromboxane B2 (TXB2) samples were obtained at the end of each treatment period. Placebo was compared with each dose of ASA for each group. In both the enalapril and losartan groups, mean, systolic, and diastolic BP were unchanged with the addition of ASA. Concentrations of TXB2 were suppressed to <10% in both groups with ASA. This study demonstrates that 81 to 325 mg/day ASA exerts no significant effect on BP in essential hypertensives taking enalapril or losartan.


Subject(s)
Angiotensin-Converting Enzyme Inhibitors/therapeutic use , Antihypertensive Agents/therapeutic use , Aspirin/pharmacology , Blood Pressure/drug effects , Cyclooxygenase Inhibitors/pharmacology , Enalapril/therapeutic use , Hypertension/physiopathology , Losartan/therapeutic use , Adult , Blood Pressure/physiology , Cross-Over Studies , Double-Blind Method , Drug Interactions , Female , Humans , Hypertension/drug therapy , Male , Middle Aged , Patient Compliance , Thromboxane B2/blood
2.
Hosp Pract (1995) ; 33(5): 141-4, 149-51, 156 passim, 1998 May 15.
Article in English | MEDLINE | ID: mdl-9606359

ABSTRACT

Inflammatory bowel disease is a spectrum of disorders whose etiology and pathogenesis are unclear. No therapy is standard; many modalities exist for management. New drugs, improved formulations of existing drugs, combination therapy and biologic agents offer more effective relief and maintain disease remission.


Subject(s)
Inflammatory Bowel Diseases/drug therapy , Adult , Anti-Inflammatory Agents, Non-Steroidal/therapeutic use , Antibodies, Monoclonal/therapeutic use , Azathioprine/therapeutic use , Female , Humans , Immunosuppressive Agents/therapeutic use , Inflammatory Bowel Diseases/etiology , Mesalamine/therapeutic use , Tumor Necrosis Factor-alpha/immunology
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