Key result
Antenatal betamethasone exposure in uninephrectomized rams significantly lowered basal sodium excretion, increased mean arterial pressure, and enhanced the decrease in sodium excretion from Ang-(1-7).
Why the study?
Does antenatal betamethasone exposure alter renal responses to angiotensin-(1-7) in uninephrectomized adult male sheep?
Does antenatal betamethasone exposure alter renal responses to angiotensin-(1-7) in uninephrectomized adult male sheep?
Antenatal betamethasone exposure impairs renal function and alters renal responses to angiotensin-(1-7) via AT1R activation in adult uninephrectomized rams.
Antenatal steroid exposure may program offspring renal RAS responses; leaves open human relevance and requires clinical confirmation.
Antenatal corticosteroid exposure reduces renal function and alters the intrarenal renin-angiotensin system to favor angiotensin activation of angiotensin type 1 receptor (AT1R) mediated responses in ovine offspring. This study aimed to assess whether antenatal steroid exposure would affect renal responses to the direct intrarenal infusion of angiotensin-(1-7) in rams and the angiotensin receptors involved in mediating responses to the peptide. Adult, uninephrectomized rams exposed to either betamethasone or vehicle before birth received intrarenal angiotensin-(1-7) infusions (1 ng/kg/min) alone or in combination with antagonists to angiotensin receptors for 3 h. Basal sodium excretion (UNa) was significantly lower and mean arterial pressure was significantly higher in betamethasone- compared to the vehicle-treated sheep. Angiotensin-(1-7) decreased UNa more in betamethasone- than in vehicle-treated sheep. Candesartan reversed the response to angiotensin-(1-7) but D-Ala(7)-angiotensin-(1-7) did not. Angiotensin-(1-7) infusion decreased effective renal plasma flow in both groups to a similar extent and the response was reversed by candesartan, but was not blocked by D-Ala(7)-angiotensin-(1-7). Glomerular filtration rate increased significantly in both groups after 3 h infusion of angiotensin-(1-7) plus candesartan. These results suggest that antenatal exposure to a clinically relevant dose of betamethasone impairs renal function in rams. Moreover, angiotensin-(1-7) appears capable of activating the AT1R in uninephrectomized rams.
No takes yet. Share an insight, caveat, or question.
Bi et al. (2012) studied Antenatal corticosteroid exposure. Antenatal betamethasone exposure and intrarenal angiotensin-(1-7) infusion vs. Vehicle was evaluated on Renal responses (basal sodium excretion, mean arterial pressure, effective renal plasma flow, glomerular filtration rate). Antenatal betamethasone exposure in uninephrectomized rams significantly lowered basal sodium excretion, increased mean arterial pressure, and enhanced the decrease in sodium excretion from Ang-(1-7).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: