Why the study?
Does long-term treatment with a hydrochlorothiazide mixture improve baroreflex sensitivity and prevent organ damage in spontaneously hypertensive rats?
Does long-term treatment with a hydrochlorothiazide mixture improve baroreflex sensitivity and prevent organ damage in spontaneously hypertensive rats?
Long-term treatment with a low-dose hydrochlorothiazide mixture prevents hypertensive organ damage in spontaneously hypertensive rats, partly through the restoration of arterial baroreflex function.
Answers are grounded in this paper and cite their sources.
Supports baroreflex restoration as target in hypertension models; leaves open human translation and clinical testing.
Hydrochlorothiazide mixture (HCTM) is widely used in China for the treatment of hypertension. This mixture consists of hydrochlorothiazide, triamterene, reserpine, hydralazine and chlordiazpoxide, with small (one-third to one-fifth of normal) doses of each drug. The present study was designed to investigate the effects of this mixture on blood pressure, blood pressure variability (BPV), baroreflex sensitivity (BRS) and end-organ damage in spontaneously hypertensive rats (SHR). 2. The HCTM was mixed in the rat chow and rats were treated for 4 months. After treatment, rats were catheterized and their blood pressure, BPV and BRS were measured in the conscious state. Organ damage was examined after these measurements had been completed. 3. It was found that HCTM not only decreased blood pressure and BPV, but also ameliorated impaired BRS in SHR. The HCTM had an obvious effect on organ protection in SHR. 4. The HCTM prevented left ventricular hypertrophy and this effect was mainly related to a decrease in systolic blood pressure. The effects of HCTM on preventing renal atrophy were mainly determined by BRS. Baroreflex sensitivity was the most important determinant for predicting organ damage in HCTM-treated SHR. 5. In conclusion, long-term treatment of rats with HCTM prevented hypertensive organ damage. Restoration of arterial baroreflex function contributes to organ protection in SHR treated in the long term with HCTM.
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Lu et al. (2003) studied this question.
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