期刊
BRAIN RESEARCH
卷 890, 期 1, 页码 38-48出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/S0006-8993(00)03027-4
关键词
blood-brain barrier; blood flow; potassium transport; insulin transport; perfusion
资金
- NIDA NIH HHS [F32 DA006037-01, DA-11271, DA-06037, F32 DA006037-02, F32 DA006037-04, F32 DA006037-03, F32 DA006037] Funding Source: Medline
- NINDS NIH HHS [NS-39592] Funding Source: Medline
Pathological states (i.e. stroke, cardiac arrest) can lead to reduced blood Row to the brain potentially altering blood-brain barrier (BBB) permeability and regulatory transport functions. BBB disruption leads to increased cerebrovascular permeability, an important factor in the development of ischemic brain injury and edema formation. In this study, reduced flow was investigated to determine the effects on cerebral blood flow (CBF), pressure, basal BBB permeability, and transport of insulin and K+ across the BBB. Anesthetized adult female Sprague-Dawley rats were measured at normal flow (3.1 ml min(-1)), half flow (1.5 ml min(-1)), and quarter flow (0.75 ml min(-1)), using bilateral in situ brain perfusion for 20 min followed by capillary depletion analysis. Reduction in perfusion flow rates demonstrated a modest reduction in CBF (1.27-1.56 ml min(-1) g(-1)), a decrease in pressure, and no significant effect on basal BBB permeability indicating that autoregulation remained functional. In contrast, there was a concomittant decrease in BBB transport of both insulin and K+ with reduced flow. At half and quarter flow, insulin transport was significantly reduced (R-Br%=17.2 and R-Br%=16.2, respectively) from control (R-Br%=30.4). Additionally, a significant reduction in [Rb-86(+)] was observed at quarter flow (R-Br%=2.5) as compared to control (R-Br%=4.8) suggesting an alteration in ion homeostasis as a result of low flow. This investigation suggests that although autoregulation maintains CBF, BBB transport mechanisms were significantly compromised in states of reduced flow. These flow alterations may have a significant impact on brain homeostasis in pathological states. (C) 2001 Elsevier Science B.V. All rights reserved.
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