Search results for "Captopril"

showing 10 items of 40 documents

Captopril does not affect plasma endothelin-1 during thrombolysis and reperfusion.

1995

Studies showed that endothelin-1 (ET-1) was increased in the acute myocardial infarction (AMI). Experimental studies reported that captopril was able to reduce ET-1 secretion, and that ET-1 was increased during reperfusion. This study was aimed to verify if captopril was able to reduce plasma ET-1 during thrombolysis in AMI. Seventy-three patients, hospitalized for suspected AMI within 4 h from the onset of symptoms suitable for thrombolysis (1st episode), Killip class 1-2, were randomized (double blind) into two groups: group 1 (37 pts), 8 F/29 M, received captopril, 6.25 mg, orally 15 min before thrombolysis. Group 2: (36 pts) 8 F/28 M, received placebo before thrombolysis. All patients m…

Malemedicine.medical_specialtyCaptoprilTime Factorsmedicine.medical_treatmentMyocardial InfarctionAdministration OralAngiotensin-Converting Enzyme InhibitorsBlood PressureMyocardial ReperfusionPlaceboAnginaPlacebosElectrocardiographyDouble-Blind MethodHeart RateInternal medicineFibrinolysismedicineHumansThrombolytic TherapyMyocardial infarctionAngina UnstableCreatine KinaseKillip classbusiness.industryUnstable anginaEndothelinsCaptoprilThrombolysismedicine.diseaseRecombinant ProteinsSurgeryIsoenzymesTissue Plasminogen ActivatorCardiologyFemaleCardiology and Cardiovascular Medicinebusinessmedicine.drugInternational journal of cardiology
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The combination ace-inhibitors plus canreonate in patients with anterior myocardial infarction: safety and tolerability study.

2001

There is recent evidence that aldosterone (ALDO) exerts pro-fibrotic effects, acting via the mineral-corticoid receptors in cardiovascular tissues and partial aldosterone escape during ACE-inhibition treatment occurs.A double blind randomised study was performed to evaluate the feasibility, and tolerability of the administration of the 25 mg/day of canreonate plus captopril versus captopril alone in patients with anterior AMI unsuitable for thrombolysis and/or not receiving thrombolytic treatment, and unreperfused after thrombolysis. Fifty five patients hospitalised for anterior AMI,with a serum creatinine concentration2.0 mg/dl and a serum K concentration5.0 mmol per liter were randomised …

Malemedicine.medical_specialtyCaptoprilmedicine.medical_treatmentAldosterone escapeUrologyMyocardial InfarctionAngiotensin-Converting Enzyme Inhibitorschemistry.chemical_compoundDouble-Blind MethodmedicineHumanscardiovascular diseasesMyocardial infarctionAgedCreatinineE/A ratiobusiness.industryCaptoprilThrombolysisMiddle Agedmedicine.diseaseSurgerychemistryTolerabilityACE inhibitorFeasibility StudiesDrug Therapy CombinationFemaleCanrenoic AcidCardiology and Cardiovascular Medicinebusinessmedicine.drugInternational journal of cardiology
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Characterization of diorganotin(IV) complexes with captopril. The first crystallographically authenticated metal complex of this anti-hypertensive ag…

2003

Abstract Diorganotin(IV) complexes R 2 Sn(cap) (capH 2 = N -[( S )-3-mercapto-2-methylpropionyl]- l -proline; R=Me, Et, n -Bu and t -Bu) were prepared and characterised. The FTIR and Raman spectra demonstrated that the organotin(IV) moieties interact with the {S} atom of the ligand, while the other coordination sites are the carboxylate and the amide –CO groups. Mossbauer Δ data showed that the diorganotin(IV) compounds adopt slightly distorted trigonal-bipyramidal (tbp) geometry. A single-crystal X-ray study was performed on the compound Me 2 Sn(cap): the Sn atom is five-coordinated in a distorted tbp environment, with two {O} atoms in the axial positions and the {S} and two {C} atoms in t…

Models MolecularCaptoprilMagnetic Resonance SpectroscopyCrystallography X-RaySpectrum Analysis RamanBiochemistryInorganic ChemistryMetalSpectroscopy Mossbauerchemistry.chemical_compoundsymbols.namesakeAmideSpectroscopy Fourier Transform InfraredMössbauer spectroscopyAtomOrganotin CompoundsCarboxylateFourier transform infrared spectroscopyAntihypertensive AgentsLigandCrystallographychemistryvisual_artsymbolsvisual_art.visual_art_mediumRaman spectroscopyJournal of Inorganic Biochemistry
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Changes of the renin-angiotensin and of the kallikrein-kinin system after administration of saline, christalloid and colloid solution in the rat. Eff…

1988

PharmacologyBlood VolumeCaptoprilChemistrymedicine.medical_treatmentCaptoprilKininsKininPharmacologySodium ChlorideRatsRenin-Angiotensin SystemSolutionsColloidGlucoseFurosemideRenin–angiotensin systemmedicineAnimalsKallikreinsColloidsSalinemedicine.drugPharmacological research communications
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ACE inhibitor potentiation of bradykinin-induced venoconstriction

1997

1. Angiotensin-converting enzyme (ACE) inhibitors exert their cardiovascular effects not only by preventing the formation of angiotensin II (AII), but also by promoting the accumulation of bradykinin in or at the vessel wall. In addition, certain ACE inhibitors have been shown to augment the vasodilator response to bradykinin, presumably by an interaction at the level of the B2 receptor. We have investigated whether this is a specific effect of the ACE inhibitor class of compounds in isolated endothelium-denuded segments of the rabbit jugular vein where bradykinin elicits a constrictor response which is exclusively mediated by activation of the B2 receptor. 2. Moexiprilat and ramiprilat (< …

PharmacologyRamiprilmedicine.medical_specialtybiologyEnalaprilatBradykininAngiotensin-converting enzymeCaptoprilchemistry.chemical_compoundEndocrinologychemistryInternal medicineACE inhibitorcardiovascular systemmedicinebiology.proteinBradykinin receptorRamiprilatmedicine.drugBritish Journal of Pharmacology
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Long-term treatment with the ace inhibitor captopril, alone or in combination with hydrochlorothiazide, in elderly hypertensives: Effects on blood pr…

1993

Abstract The efficacy and tolerability of long-term treatment with the angiotensin converting enzyme inhibitor captopril was evaluated in elderly hypertensive subjects. One hundred thirty patients were studied (61 men and 69 women; mean age, 68.33 ± 5.49 years), all with mild to moderate arterial hypertension (mild = 90–105 mmHg; moderate = 105–115 mmHg). Patients with secondary hypertension were excluded from the study. After a 2-week drug washout, patients were given captopril 25 to 100 mg/day alone or in combination with hydrochlorothiazide (HCTZ) 25 mg/day for 15 weeks. After 2 weeks of treatment, significant decreases in systolic and diastolic blood pressures were observed (P

Pharmacologymedicine.medical_specialtybiologybusiness.industryUrologyHemodynamicsAngiotensin-converting enzymeCaptoprilEndocrinologyBlood pressureHydrochlorothiazideTolerabilityInternal medicineACE inhibitormedicinebiology.proteinPharmacology (medical)businessThiazidemedicine.drugCurrent Therapeutic Research
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Effects of captopril on plasma endothelin-1 during thrombolysis: Preliminary findings

1995

Pharmacologymedicine.medical_specialtybusiness.industrymedicine.medical_treatmentInfarctionCaptoprilGeneral MedicineThrombolysismedicine.diseaseEndothelin 1Text miningInternal medicinemedicineCardiologyPharmacology (medical)Cardiology and Cardiovascular Medicinebusinessmedicine.drugCardiovascular Drugs and Therapy
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Effects of administration of captopril, metoprolol, and the captopril-metoprolol combination as adjuvant therapy during thrombolysis in acute myocard…

1994

Pharmacologymedicine.medical_specialtybusiness.industrymedicine.medical_treatmentInfarctionCaptoprilGeneral MedicineThrombolysismedicine.diseaseInternal medicinemedicineCardiologyAdjuvant therapyPharmacology (medical)Myocardial infarctionCardiology and Cardiovascular MedicinebusinessMetoprololmedicine.drugCardiovascular Drugs and Therapy
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Pathological role of a constitutively active population of α1D -adrenoceptors in arteries of spontaneously hypertensive rats

2002

The role of a constitutively active population of α1D-adrenoceptors was analysed in arteries obtained from spontaneously hypertensive rats (SHR) and controls (WKY) divided into three groups: young prehypertensive, adult hypertensive, and adult animals chronically treated with captopril (50 mg kg−1 per day orally) in order to prevent the hypertensive state. In adult SHR, a significant increase in BMY 7378 potency (not in prazosin potency) was observed in aorta, mesenteric artery, and the first and second branches of the small mesenteric arteries with respect to WKY rats. This difference was not observed in iliac and tail arteries, which suggests an increased functional role of α1D-adrenocept…

Pharmacologymedicine.medical_specialtyeducation.field_of_studyAortabusiness.industryPopulationCaptoprilVasodilationEndocrinologymedicine.anatomical_structureInternal medicinemedicine.arteryCirculatory systemmedicinePrazosinmedicine.symptombusinesseducationMesenteric arteriesVasoconstrictionmedicine.drugBritish Journal of Pharmacology
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An ab initio conformational study on captopril

2003

Abstract Captopril can interact regio- and stereo-specifically with various functional groups present at the active site of angiotensin converting enzyme (ACE). Since no X-ray structure of ACE is available, Captopril, as an ACE inhibitor may be used as a ‘molecular caliper’, to estimate upper and lower bound values for separation d, where the mercaptidic terminal group of the molecule is linked to the enzyme Zn2+ cofactor, while the carboxylate links via an hydrogen bond to the guanidine moiety of an arginine side chain. As the results of this Ab Initio study, the conformations of the dianionic form of the full captopril molecule are reported here.

biologyStereochemistryHydrogen bondAb initioActive siteCaptoprilAngiotensin-converting enzymeCondensed Matter PhysicsBiochemistrychemistry.chemical_compoundchemistryACE inhibitorbiology.proteinmedicineMoietyPhysical and Theoretical ChemistryGuanidinemedicine.drugJournal of Molecular Structure: THEOCHEM
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