Estrogen and insulin transport through the blood-brain barrier.

May AA, Bedel ND, Shen L, Woods SC, Liu M
Physiol Behav. 2016 163: 312-321

PMID: 27182046 · PMCID: PMC4947438 · DOI:10.1016/j.physbeh.2016.05.019

Obesity is associated with insulin resistance and reduced transport of insulin through the blood-brain barrier (BBB). Reversal of high-fat diet-induced obesity (HFD-DIO) by dietary intervention improves the transport of insulin through the BBB and the sensitivity of insulin in the brain. Although both insulin and estrogen (E2), when given alone, reduce food intake and body weight via the brain, E2 actually renders the brain relatively insensitive to insulin's catabolic action. The objective of these studies was to determine if E2 influences the ability of insulin to be transported into the brain, since the receptors for both E2 and insulin are found in BBB endothelial cells. E2 (acute or chronic) was systemically administered to ovariectomized (OVX) female rats and male rats fed a chow or a high-fat diet. Food intake, body weight and other metabolic parameters were assessed along with insulin entry into the cerebrospinal fluid (CSF). Acute E2 treatment in OVX female and male rats reduced body weight and food intake, and chronic E2 treatment prevented or partially reversed high-fat diet-induced obesity. However, none of these conditions increased insulin transport into the CNS; rather, chronic E2 treatment was associated less-effective insulin transport into the CNS relative to weight-matched controls. Thus, the reduction of brain insulin sensitivity by E2 is unlikely to be mediated by increasing the amount of insulin entering the CNS.

Copyright © 2016 Elsevier Inc. All rights reserved.

MeSH Terms (18)

Animals ATP Binding Cassette Transporter, Subfamily B, Member 1 Blood-Brain Barrier Blood Vessels Body Weight Brain Dietary Fats Estrogens Female Glucose Transporter Type 1 Insulin Insulin Resistance Male Obesity Ovariectomy Rats Rats, Long-Evans Synaptophysin

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