TY - JOUR
T1 - Pathways for insulin access to the brain
T2 - the role of the microvascular endothelial cell
AU - Meijer, Rick I
AU - Gray, Sarah M
AU - Aylor, Kevin W
AU - Barrett, Eugene J
N1 - Copyright © 2016 the American Physiological Society.
PY - 2016/11/1
Y1 - 2016/11/1
N2 - Insulin affects multiple important central nervous system (CNS) functions including memory and appetite, yet the pathway(s) by which insulin reaches brain interstitial fluid (bISF) has not been clarified. Recent studies demonstrate that to reach bISF, subarachnoid cerebrospinal fluid (CSF) courses through the Virchow-Robin space (VRS) which sheaths penetrating pial vessels down to the capillary level. Whether insulin predominantly enters the VRS and bISF by local transport through the blood-brain barrier, or by being secreted into the CSF by the choroid plexus, is unknown. We injected 125I-TyrA14-insulin or regular insulin intravenously and compared the rates of insulin reaching subarachnoid CSF with its plasma clearance by brain tissue samples (an index of microvascular endothelial cell binding/uptake/transport). The latter process was more than 40-fold more rapid. We then showed that selective insulin receptor blockade or 4 wk of high-fat feeding each inhibited microvascular brain 125I-TyrA14-insulin clearance. We further confirmed that 125I-TyrA14-insulin was internalized by brain microvascular endothelial cells, indicating that the in vivo tissue association reflected cellular transport, not simply microvascular tracer binding.
AB - Insulin affects multiple important central nervous system (CNS) functions including memory and appetite, yet the pathway(s) by which insulin reaches brain interstitial fluid (bISF) has not been clarified. Recent studies demonstrate that to reach bISF, subarachnoid cerebrospinal fluid (CSF) courses through the Virchow-Robin space (VRS) which sheaths penetrating pial vessels down to the capillary level. Whether insulin predominantly enters the VRS and bISF by local transport through the blood-brain barrier, or by being secreted into the CSF by the choroid plexus, is unknown. We injected 125I-TyrA14-insulin or regular insulin intravenously and compared the rates of insulin reaching subarachnoid CSF with its plasma clearance by brain tissue samples (an index of microvascular endothelial cell binding/uptake/transport). The latter process was more than 40-fold more rapid. We then showed that selective insulin receptor blockade or 4 wk of high-fat feeding each inhibited microvascular brain 125I-TyrA14-insulin clearance. We further confirmed that 125I-TyrA14-insulin was internalized by brain microvascular endothelial cells, indicating that the in vivo tissue association reflected cellular transport, not simply microvascular tracer binding.
KW - Animals
KW - Biological Transport
KW - Blood-Brain Barrier/metabolism
KW - Cerebrospinal Fluid/metabolism
KW - Diet, High-Fat
KW - Endothelial Cells/metabolism
KW - Enzyme-Linked Immunosorbent Assay
KW - Extracellular Fluid/metabolism
KW - Glucose Clamp Technique
KW - Hypoglycemic Agents/pharmacokinetics
KW - In Vitro Techniques
KW - Injections, Intravenous
KW - Injections, Intraventricular
KW - Insulin/pharmacokinetics
KW - Iodine Radioisotopes
KW - Male
KW - Microvessels/metabolism
KW - Pia Mater/blood supply
KW - Rats
KW - Rats, Sprague-Dawley
KW - Receptor, Insulin/antagonists & inhibitors
KW - Subarachnoid Space/metabolism
U2 - 10.1152/ajpheart.00081.2016
DO - 10.1152/ajpheart.00081.2016
M3 - Article
C2 - 27591216
SN - 0363-6135
VL - 311
SP - H1132-H1138
JO - American Journal of Physiology. Heart and Circulatory Physiology
JF - American Journal of Physiology. Heart and Circulatory Physiology
IS - 5
ER -