The blood-brain barrier as an endocrine tissue

被引:118
作者
Banks, William A. [1 ,2 ]
机构
[1] Vet Affairs Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA 98108 USA
[2] Univ Washington, Sch Med, Dept Med, Div Gerontol & Geriatr Med, Seattle, WA 98195 USA
关键词
CEREBROSPINAL FLUID BARRIER; NECROSIS-FACTOR-ALPHA; SERUM LEPTIN LEVELS; ENDOTHELIAL-CELLS; INTRACEREBROVENTRICULAR INJECTION; BODY-WEIGHT; INSULIN TRANSPORT; P-GLYCOPROTEIN; ALZHEIMERS-DISEASE; IMPAIRED TRANSPORT;
D O I
10.1038/s41574-019-0213-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The blood-brain barrier (BBB) was first noted for its ability to prevent the unregulated exchange of substances between the blood and the central nervous system (CNS). Over time, its characterization as an interface that enables regulated exchanges between the CNS and substances that are carried in the blood in a hormone-like fashion have emerged. Therefore, communication between the CNS, BBB and peripheral tissues has many endocrine-like properties. In this Review, I examine the various ways in which the BBB exhibits endocrine-related properties. The BBB is a target for hormones, such as leptin and insulin, that affect many of its functions. The BBB is also a secretory body, releasing substances either into the blood or the interstitial fluid of the brain. The BBB selectively allows classical and non-classical hormones entry to and exit from the CNS, thus allowing the CNS to be both an endocrine target and a secretory tissue. The BBB is affected by endocrine diseases such as diabetes mellitus and can cause or participate in endocrine diseases, including those related to thyroid hormones and obesity. The endocrine-like mechanisms of the BBB can extend the definition of endocrine disease to include neurodegenerative conditions, including Alzheimer disease, and of hormones to include cytokines, triglycerides and fatty acids.
引用
收藏
页码:444 / 455
页数:12
相关论文
共 160 条
[1]   Occipital blood-brain barrier permeability is an independent predictor of visual outcome in type 2 diabetes, irrespective of the retinal barrier: A longitudinal study [J].
Abuhaiba, S. I. ;
Cordeiro, M. ;
Amorim, A. ;
Cruz, A. ;
Quendera, B. ;
Ferreira, C. ;
Ribeiro, L. ;
Bernardes, R. ;
Castelo-Branco, M. .
JOURNAL OF NEUROENDOCRINOLOGY, 2018, 30 (01)
[2]   Triglycerides cross the blood-brain barrier and induce central leptin and insulin receptor resistance [J].
Banks, W. A. ;
Farr, S. A. ;
Salameh, T. S. ;
Niehoff, M. L. ;
Rhea, E. M. ;
Morley, J. E. ;
Hanson, A. J. ;
Hansen, K. M. ;
Craft, S. .
INTERNATIONAL JOURNAL OF OBESITY, 2018, 42 (03) :391-397
[3]  
Banks W A, 1993, Rev Neurosci, V4, P365
[4]   Partial saturation and regional variation in the blood-to-brain transport of leptin in normal weight mice [J].
Banks, WA ;
Clever, CM ;
Farrell, CL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2000, 278 (06) :E1158-E1165
[5]   Impaired transport of leptin across the blood-brain barrier in obesity is acquired and reversible [J].
Banks, WA ;
Farrell, CL .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (01) :E10-E15
[6]   Extent and direction of ghrelin transport across the blood-brain barrier is determined by its unique primary structure [J].
Banks, WA ;
Tschöp, M ;
Robinson, SM ;
Heiman, ML .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 302 (02) :822-827
[7]   Leptin enters the brain by a saturable system independent of insulin [J].
Banks, WA ;
Kastin, AJ ;
Huang, WT ;
Jaspan, JB ;
Maness, LM .
PEPTIDES, 1996, 17 (02) :305-311
[8]   Impaired transport of leptin across the blood-brain barrier in obesity [J].
Banks, WA ;
DiPalma, CR ;
Farrell, CL .
PEPTIDES, 1999, 20 (11) :1341-1345
[9]   Triglycerides induce leptin resistance at the blood-brain barrier [J].
Banks, WA ;
Coon, AB ;
Robinson, SM ;
Moinuddin, A ;
Shultz, JM ;
Nakaoke, R ;
Morley, JE .
DIABETES, 2004, 53 (05) :1253-1260
[10]   TRANSPORT OF THYROXINE ACROSS THE BLOOD-BRAIN-BARRIER IS DIRECTED PRIMARILY FROM BRAIN TO BLOOD IN THE MOUSE [J].
BANKS, WA ;
KASTIN, AJ ;
MICHALS, EA .
LIFE SCIENCES, 1985, 37 (25) :2407-2414