CGS 35601 and its Orally Active Prodrug CGS 37808 as Triple Inhibitors of Endothelin-converting Enzyme-1, Neutral Endopeptidase 24.11, and Angiotensin-converting Enzyme

التفاصيل البيبلوغرافية
العنوان: CGS 35601 and its Orally Active Prodrug CGS 37808 as Triple Inhibitors of Endothelin-converting Enzyme-1, Neutral Endopeptidase 24.11, and Angiotensin-converting Enzyme
المؤلفون: Michael E. Beil, Arco Y. Jeng, Charles W. Bruseo, Angelo J. Trapani, Fariborz Firooznia, Paula Savage
المصدر: Journal of Cardiovascular Pharmacology. 44:S211-S215
بيانات النشر: Ovid Technologies (Wolters Kluwer Health), 2004.
سنة النشر: 2004
مصطلحات موضوعية: Male, medicine.medical_specialty, Indoles, Time Factors, Endothelin converting enzyme 1, medicine.medical_treatment, Administration, Oral, Angiotensin-Converting Enzyme Inhibitors, Blood Pressure, CHO Cells, Endothelin-Converting Enzymes, Peptidyl-Dipeptidase A, Pharmacology, Transfection, Rats, Sprague-Dawley, Cricetulus, Atrial natriuretic peptide, Cricetinae, Internal medicine, Renin–angiotensin system, medicine, Animals, Aspartic Acid Endopeptidases, Humans, Prodrugs, Protease Inhibitors, education, Neprilysin, education.field_of_study, Endothelin-1, biology, Chemistry, Angiotensin II, Metalloendopeptidases, Angiotensin-converting enzyme, Dipeptides, Prodrug, Rats, Endocrinology, Injections, Intravenous, biology.protein, Rabbits, Diuretic, Cardiology and Cardiovascular Medicine, Atrial Natriuretic Factor
الوصف: CGS 35601 is a potent triple inhibitor of endothelinconverting enzyme-1, neutral endopeptidase 24.11, and angiotensinconverting enzyme. It inhibited the activities of these three enzymes with IC50 values of 55, 2 and 22 nM, respectively. In conscious rats, CGS 35601 suppressed the big endothelin-1-induced pressor response by 82% and 72% at 30 and 120 minutes, respectively, following injection at a dose of 10 mg/kg, intravenously. At the same dose, CGS 35601 increased plasma atrial natriuretic peptide (ANP) immunoreactivity by 170% for up to 4 hours in conscious rats infused with ANP, and it inhibited the angiotensin I-induced pressor response by 74-94% within the first 2 hours after dosing. Similar in vivo activities were also observed with its orally active prodrug, CGS 37808. This compound blocked the big endothelin-1- induced pressor response by 71% and 67% at 30 and 120 minutes, respectively, after an oral dose of 10 mgEq/kg in conscious rats. It also increased plasma ANP immunoreactivity by 103% for up to 4 hours and inhibited the angiotensin I-induced pressor response by an average of 49% within the first 4 hours after the same dosing regimen. By suppressing the biosyntheses of endothelin-1 and angiotensin II, two potent vasoconstrictors, while simultaneously potentiating the circulating levels of ANP, a vasorelaxant and diuretic, CGS 35601 and CGS 37808 may represent novel agents for the treatment of cardiovascular and renal diseases.
تدمد: 0160-2446
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fce19180c663a92a9de8fa97a727250c
https://doi.org/10.1097/01.fjc.0000166237.57077.d6
رقم الأكسشن: edsair.doi.dedup.....fce19180c663a92a9de8fa97a727250c
قاعدة البيانات: OpenAIRE