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1.
Hypertens Res ; 40(10): 892-898, 2017 Oct 05.
Article in English | MEDLINE | ID: mdl-28446804

ABSTRACT

In patients with insufficient blood pressure (BP) control, despite using a combination regimen containing an angiotensin receptor blocker and a calcium channel blocker (CCB), whether a greater dose of CCB or adding a diuretic is more effective at lowering BP remains unclear. We conducted a multicenter randomized clinical trial to compare the efficacy of switching from the daily administration of a single-pill fixed-dose combination of irbesartan (100 mg) and amlodipine (5 mg) to irbesartan (100 mg) with an increased dose of amlodipine (10 mg) (HD group, n=62) or irbesartan (100 mg) and amlodipine (5 mg) with 1 mg of indapamide (D group, n=63) in patients with poorly controlled hypertension. BP measured at home was monitored by a physician using a telemonitoring system. Between the HD and D groups, no significant differences were observed in morning home BP changes (mean reduction of systolic/diastolic BP, 1.7/0.9 mmHg; 95% confidence intervals, -2.4 to 5.7/-1.4 to 3.2; P=0.19/0.37), achievement rate of target BP (45.2% vs. 42.9%, P=0.80), BP variability independent of the mean (P⩾0.74), other variability indices (P⩾0.55) and time to stabilization, which was calculated using a fitted analysis (13.1 days vs. 11.4 days, P=0.99). Although a significant increase in serum uric acid was observed in the D group (P<0.0001), neither clinically relevant abnormal laboratory test results nor critical BP changes were observed throughout the trial period. Both antihypertensive drug combination strategies were effective treatment options. Further investigation is required to determine the appropriate use of both therapies based on the various pathologies associated with hypertension.


Subject(s)
Amlodipine/therapeutic use , Antihypertensive Agents/therapeutic use , Biphenyl Compounds/therapeutic use , Calcium Channel Blockers/therapeutic use , Diuretics/therapeutic use , Hypertension/drug therapy , Tetrazoles/therapeutic use , Adult , Aged , Amlodipine/administration & dosage , Antihypertensive Agents/administration & dosage , Biphenyl Compounds/administration & dosage , Blood Pressure/drug effects , Calcium Channel Blockers/administration & dosage , Diuretics/administration & dosage , Dose-Response Relationship, Drug , Drug Therapy, Combination , Female , Humans , Irbesartan , Male , Middle Aged , Tetrazoles/administration & dosage , Treatment Outcome
2.
J Pharm Pharmacol ; 62(12): 1740-5, 2010 Dec.
Article in English | MEDLINE | ID: mdl-21054400

ABSTRACT

OBJECTIVES: Amlodipine, a calcium channel blocker (CCB), is one of the most common antihypertensive medicines in Japan. We evaluated whether the calcium channel blocker confers cardiac protection through the renin-angiotensin-aldosterone system in male stroke-prone spontaneously hypertensive rats (SHR-SP). METHODS: Fifteen week-old rats were divided into 2 groups: amlodipine group (3 mg/kg/day, n = 5) and control group (n = 5). KEY FINDINGS: The CCB lowered systolic blood pressure significantly (P < 0.05). Plasma aldosterone concentration in the amlodipine group was remarkably lower than in the control group (P < 0.05), but plasma renin activity and plasma angiotensin II concentration were not different between the two groups. The CCB also suppressed the mRNA expression of brain natriuretic peptide, transforming growth factor-ß1, and fibronectin extracted from the left ventricle. CONCLUSIONS: These results suggest that amlodipine attenuates cardiac damage by lowering plasma aldosterone concentration in hypertensive rats with developing arteriosclerosis.


Subject(s)
Amlodipine/pharmacology , Antihypertensive Agents/pharmacology , Cardiotonic Agents/pharmacology , Fibronectins/genetics , Heart/drug effects , Hypertension/drug therapy , Myocardium/metabolism , Natriuretic Peptide, Brain/genetics , Transforming Growth Factor beta/genetics , Aldosterone/blood , Angiotensin II/blood , Animals , Antihypertensive Agents/metabolism , Blood Pressure/drug effects , Calcium Channel Blockers/pharmacology , Fibronectins/metabolism , Gene Expression Regulation/drug effects , Heart/physiopathology , Hypertension/genetics , Hypertension/physiopathology , Male , Natriuretic Peptide, Brain/metabolism , Rats , Rats, Inbred SHR , Renin/blood , Renin-Angiotensin System/drug effects , Transforming Growth Factor beta/metabolism
3.
Int J Cardiol ; 136(3): e66-8, 2009 Aug 21.
Article in English | MEDLINE | ID: mdl-18674830

ABSTRACT

Isolated noncompaction of the ventricular myocardium (INVM) is an unclassified cardiomyopathy and is thought to be due to arrest of myocardial morphogenesis. Left ventricular failure and ventricular arrhythmias may occur in approximately half of the patients and account for half of the death in this disorder. In this report, we describe a patient with INVM in whom cardiac resynchronization and cardioverter defibrillation therapy was effective for the improvement of left ventricular function and for the prevention of ventricular arrhythmias.


Subject(s)
Cardiac Pacing, Artificial , Cardiomyopathies/therapy , Electric Countershock , Ventricular Dysfunction, Left/therapy , Cardiomyopathies/diagnostic imaging , Cardiomyopathies/pathology , Defibrillators, Implantable , Echocardiography , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Ventricular Dysfunction, Left/diagnostic imaging , Ventricular Dysfunction, Left/pathology
5.
Opt Express ; 12(10): 2070-80, 2004 May 17.
Article in English | MEDLINE | ID: mdl-19475042

ABSTRACT

We have demonstrated a carrier-envelope phase (CEP) stabilized chirped-pulse amplification (CPA) system employing a grating-based pulse stretcher and compressor and a regenerative amplifier for the first time. In addition to stabilizing the carrier-envelope offset phase of a laser oscillator, a new pulse selection method referenced to the carrier-envelope offset beat signal was introduced. The pulse-selection method is more robust against the carrier-envelope offset phase fluctuations than a simple pulse-clock dividing method. We observed a stable fringe in a self-referencing spectrum interferometry of the amplified pulse, which implies that the CEP of amplified pulse is stabilized. We also measured the effect of the beam angle change on the CEP of amplified pulses. The result demonstrates that the CEP stabilized CPA is scalable to higher-pulse energies.

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