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Estrogen modulation of baroreflex function in conscious mice.
Jaya Pamidimukkala1, Julia A Taylor, Wade V Welshons
1Dalton Cardiovascular Research Center, University of Missouri, Columbia, Missouri 65211, USA. PamidimukkalaJ@missouri.edu
Summary
Estrogen enhances baroreflex control of heart rate in female mice. This study found that estradiol improved the baroreflex bradycardic response to phenylephrine and angiotensin II, suggesting a sex-dependent effect.
Area of Science:
- Cardiovascular Physiology
- Neuroendocrinology
- Autonomic Neuroscience
Background:
- Estrogen is known to influence autonomic nervous system function.
- Baroreflexes are crucial for maintaining blood pressure homeostasis.
- The role of estrogen in baroreflex regulation requires further elucidation.
Purpose of the Study:
- To investigate the effects of estrogen on baroreflex regulation of heart rate in a conscious mouse model.
- To compare baroreflex responses between male and female mice with and without estradiol replacement.
Main Methods:
- Utilized a conscious mouse model with chronic arterial and venous catheterization.
- Administered phenylephrine (PE), angiotensin II (ANG II), and sodium nitroprusside (SNP) to assess baroreflex responses.
- Compared baroreflex bradycardic and tachycardic responses in male, ovariectomized female mice without estradiol (OvxE-), and ovariectomized female mice with estradiol (OvxE+).
Main Results:
- Estradiol significantly facilitated the baroreflex bradycardic response to PE in female mice (OvxE+ vs. OvxE-).
- Estradiol also significantly enhanced the baroreflex bradycardic response to ANG II in female mice (OvxE+ vs. OvxE-).
- Reflex tachycardic responses to SNP were similar across all groups.
- Male mice showed a significantly blunted baroreflex bradycardic response to ANG II compared to PE, an effect not observed in female mice.
Conclusions:
- Estrogen facilitates baroreflex function in female mice, particularly in response to pressor stimuli.
- The acute blunting of baroreflex regulation of heart rate by ANG II appears to be sex-dependent.
- These findings highlight the significant influence of sex hormones on cardiovascular autonomic control.