Sex‐ and Time‐Dependent Differences in Glutamate Receptor Subunit (GLUN1) in the Rat Rostral Ventrolateral Medulla

The cardioprotective effects of ovarian hormones are evident by the fact that women have a lower risk of cardiovascular disease compared to men, at least until menopause, at which time the relative risks reverse. Several studies have also demonstrated the importance of ovarian hormones in the regulation of sympathetic outflow, potentially via actions in the rostral ventrolateral medulla (RVLM), a brain region critical to sympathetic outflow and blood pressure. However, the time course and mechanisms of sex‐dependent changes in excitation of RVLM neurons have not been fully characterized. Therefore, the purpose of this study was to compare glutamate receptor (GluN1) subunit expression in the RVLM of male and female rats, focusing specifically on ages of development in female rats which precede the onset of the estrous cycle (4 wks old) versus when the estrous cycle is fully established (8 wks old). We hypothesized that eight week‐old female rats would exhibit reduced GluN1 compared to four week‐old females. In contrast, we also predicted that eight week‐old male rats would have higher GluN1 compared to four week‐old males. To test our hypothesis, we obtained brain punches from RVLM subregions of male and female Sprague‐Dawley rats (n=3 ea; 4 and 8 wks old) based on their anatomical location relative to the facial nucleus (FN). Punches were processed for western blotting of GluN1 subunit in four subregions: FN‐480; FN‐240; FN+240 and FN+480. At FN‐480, GluN1 was lower in eight week‐compared to four week‐old female rats (0.67 ± 0.11 vs. 1.11 ± 0.08 protein/GAPDH, respectively). In contrast, at FN‐480, eight week‐old male rats exhibited increased NR1 expression compared to four week old males (1.05 ± 0.06 vs. 0.65 ± 0.10; protein/GAPDH, respectively p<0.05). These results suggest that lower levels of ovarian hormones in prepubescent females may increase the excitability of RVLM neurons and lead to greater sympathoexcitation, which then decrease with the onset of the reproductive cycle. The absence of ovarian hormones in males (perhaps coupled with a lack of regular exercise) may exacerbate RVLM excitability, leading to greater sympathoexcitation in sedentary males. Collectively, these data suggest that ovarian hormones exert cardioprotective effects via actions in the RVLM, reducing sympathetic outflow and contributing to a lower incidence of cardiovascular disease in women of reproductive age. Support or Funding Information HL096787‐08; AHA25810010