Key result
Administration of pure mouse submaxillary gland renin to anephric rats produced dose-dependent increases in blood pressure, tissue edema, and arterial lesions.
Why the study?
Does pure submaxillary gland renin cause vascular lesions and increased vascular permeability in anephric rats?
Does pure submaxillary gland renin cause vascular lesions and increased vascular permeability in anephric rats?
Pure submaxillary gland renin alone is sufficient to produce pressor effects, increased vascular permeability, and fibrinoid necrosis in anephric rats, indicating that renin itself, rather than other renal contaminants, causes these vascular lesions.
Renin suffices for vascular injury in anephric rat models; leaves open relevance to human hypertensive disease.
In order to identify the nature of the substance(s) that causes pancreatic edema, pleural effusion, hematocrit increase, and vascular lesion upon administration of renal extracts, effects of a pure preparation of submaxillary gland renin of mouse on blood vessels were studied. This enzyme was administered intraperitoneally to conscious anehpric rats. Blood pressure elevation recorded under unrestricted conditions was proportional to pancreatic edema, pleural effusion, hematolcrit increase, and vascular lesions in small arteries and arterioles. Since the renin administered does not contain any substances and since the function of this enzyme is quite analogous to renal renin, these results have been interpreted to indicate that renin possesses both pressor and permeability activities and that the action of renin alone can account for the vascular lesions and the increased vascular permeability.
No takes yet. Share an insight, caveat, or question.
Onoyama et al. (1978) studied Anephric rats (n=48). Pure submaxillary gland renin of mouse vs. Bovine serum albumin was evaluated on Blood pressure elevation and vascular permeability/lesions. Administration of pure mouse submaxillary gland renin to anephric rats produced dose-dependent increases in blood pressure, tissue edema, and arterial lesions.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: