Key result
In a patient with Bartter's syndrome, decreased pressor responses to angiotensin II and phenylephrine were improved by various treatments, while defective chloride reabsorption was unchanged.
Why the study?
Does administration of various agents improve vascular responsiveness to angiotensin II and phenylephrine in a patient with Bartter's syndrome?
Case Report (n=1)
No
Does administration of various agents improve vascular responsiveness to angiotensin II and phenylephrine in a patient with Bartter's syndrome?
In a patient with Bartter's syndrome, decreased vascular responsiveness to angiotensin II and phenylephrine was improved by various treatments, suggesting potential vascular wall abnormalities alongside defective chloride reabsorption.
Answers are grounded in this paper and cite their sources.
Suggests vascular hyporesponsiveness may be modifiable in Bartter syndrome; leaves open generalizability beyond this single case.
In a 39-yr-old female patient with Bartter's syndrome, vascular responsiveness to angiotensin II and phenylephrine was studied. Pressor responses to angiotensin II and to phenylephrine were markedly decreased prior to treatment and were improved by administration of indomethacin, dextran, KCl, captopril, propranolol or pindolol. Moreover, the responses of total peripheral vascular resistance to angiotensin II and phenylephrine were markedly decreased before treatment and were improved by the treatment. A relatively low fractional distal chloride reabsorption was found, and that was not changed after the administration of KCl or indomethacin. The results of this patient were compatible with the primary cause of Bartter's syndrome, defective chloride reabsorption at the loop of Henle, but the possibility of an abnormality in the vascular wall could not be denied.
No takes yet. Share an insight, caveat, or question.
Ashida et al. (1992) conducted a case report in Bartter's syndrome (n=1). Pharmacological treatments (indomethacin, dextran, KCl, captopril, propranolol, pindolol) vs. Pre-treatment baseline was evaluated on Vascular responsiveness to angiotensin II and phenylephrine, and fractional distal tubular chloride reabsorption. In a patient with Bartter's syndrome, decreased pressor responses to angiotensin II and phenylephrine were improved by various treatments, while defective chloride reabsorption was unchanged.
Synapse has enriched 10 related papers. Consider them for comparative context: