Key result
Chemical renal medullectomy elevated mean arterial pressure to 142 mmHg compared with 124 mmHg in normal rats, associated with significant tachycardia and increased cardiac output.
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Hypothesis-generating for renal medullary role in BP control in rats; leaves open relevance to human hypertension.
We have investigated the mechanisms by which chemical renal medullectomy with 2-bromoethylamine hydrobromide (200 mg/kg body wt) produces hypertension in rats. Groups of chemically medullectomized rats were compared with normal rats and rats that had been partially nephrectomized to produce an equivalent fall in glomerular filtration rate. Mean arterial pressure was elevated in the medullectomized (142 +/- 6 mmHg) compared with normal rats (124 +/- 3). In the medullectomized animals this was associated with significant tachycardia (483 +/- 15 vs. 450 +/- 6 beats/min) and an increase in cardiac output (61.1 +/- 5.0 vs. 49.9 +/- 2.2 ml X min-1 X 100 g body wt-1). Plasma volume was significantly reduced in medullectomized rats (2.16 +/- 0.15 vs 3.29 +/- 0.20 ml/100 g body wt), whereas exchangeable sodium was unchanged (39.9 +/- 0.5 vs. 39.7 +/- 0.5 meq/kg body wt). By contrast, both plasma volume and exchangeable sodium were increased in partially nephrectomized rats. These results are consistent with the hypothesis that chemical medullectomy produces hypertension by increased selective sympathetic efferent activity, raising cardiac output and postcapillary venular resistance. This may be the consequence of reducing the secretion of a renomedullary humoral substance that normally inhibits such activity.
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Taverner et al. (1985) studied Hypertension. Chemical renal medullectomy with 2-bromoethylamine hydrobromide vs. Normal rats and partially nephrectomized rats was evaluated on Mean arterial pressure. Chemical renal medullectomy elevated mean arterial pressure to 142 mmHg compared with 124 mmHg in normal rats, associated with significant tachycardia and increased cardiac output.
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