The brain subfornical organ mediates leptin-induced increases in renal sympathetic activity but not its metabolic effects

CN Young, DA Morgan, SD Butler, AL Mark… - …, 2013 - Am Heart Assoc
CN Young, DA Morgan, SD Butler, AL Mark, RL Davisson
Hypertension, 2013Am Heart Assoc
The adipocyte-derived hormone leptin acts within the central nervous system to decrease
food intake and body weight and to increase renal and thermogenic brown adipose tissue
sympathetic nerve activity (SNA). Previous studies have focused on hypothalamic brain
regions, although recent findings have identified leptin receptors (ObR) in a distributed brain
network, including the circumventricular subfornical organ (SFO), a forebrain region devoid
of a blood–brain barrier. We tested the hypothesis that ObR in the SFO are functionally …
The adipocyte-derived hormone leptin acts within the central nervous system to decrease food intake and body weight and to increase renal and thermogenic brown adipose tissue sympathetic nerve activity (SNA). Previous studies have focused on hypothalamic brain regions, although recent findings have identified leptin receptors (ObR) in a distributed brain network, including the circumventricular subfornical organ (SFO), a forebrain region devoid of a blood–brain barrier. We tested the hypothesis that ObR in the SFO are functionally linked to leptin-induced decreases in food intake and body weight and increases in SNA. SFO-targeted microinjections of an adenovirus encoding Cre-recombinase in ObRflox/flox mice resulted in selective ablation of ObR in the SFO. Interestingly, deletion of ObR in the SFO did not influence the decreases in either food intake or body weight in response to daily systemic or cerebroventricular administration of leptin. In line with these findings, reduction in SFO ObR did not attenuate leptin-mediated increases in thermogenic brown adipose tissue SNA. In contrast, increases in renal SNA induced by systemic or cerebroventricular administration of leptin were abolished in mice with SFO-targeted deletion of ObR. These results demonstrate that ObR in the SFO play an important role in leptin-induced renal sympathoexcitation, but not in the body weight, food intake, or brown adipose tissue SNA thermogenic effects of leptin. These findings highlight the concept of a distributed brain network of leptin action and illustrate that brain regions, including the SFO, can mediate distinct cardiovascular and metabolic responses to leptin.
Am Heart Assoc