Murphy V A, Johanson C E
Laboratory of Neurosciences, National Institute on Aging, Bethesda, Maryland.
J Neurochem. 1989 Apr;52(4):1058-63. doi: 10.1111/j.1471-4159.1989.tb01847.x.
Sprague-Dawley rats were given treatments, known to decrease 22Na movement into choroid plexus and CSF, to investigate their effect on 22Na transfer across the cerebral capillaries. Acidic salts, acetazolamide, or amiloride was injected intraperitoneally into bilaterally nephrectomized rats, and the rate of 22Na uptake into parietal cortex, pons-medulla, and CSF was determined at 12, 18, and 24 min. Severe acidosis (arterial pH 7.2), produced by HCl injection, decreased the rate of 22Na entry into both brain regions and CSF by 25%, whereas mild acidosis (pH 7.3) from NH4Cl injection reduced brain entry by 18%, but CSF entry by only 10%. Like HCl acidosis, amiloride reduced transport into both brain and CSF by 22%. Penetration of 22Na into parietal cortex was unchanged by acetazolamide, but that into CSF was slowed 30%. Since uptake of 22Na into cortical regions is primarily movement of tracer across the cerebral capillaries when tracer uptake time is less than 30 min, the results indicate that both metabolic acidosis and amiloride decrease Na+ permeativity at the cerebral capillaries as well as at the choroid plexus. Acetazolamide, on the other hand, alters Na+ movement only across the choroidal epithelium.
给斯普拉格-道利大鼠进行已知会减少22Na进入脉络丛和脑脊液的处理,以研究其对22Na跨脑毛细血管转运的影响。将酸盐、乙酰唑胺或氨氯吡咪腹腔注射到双侧肾切除的大鼠体内,并在12、18和24分钟时测定顶叶皮质、脑桥-延髓和脑脊液中22Na的摄取率。注射HCl产生的严重酸中毒(动脉pH 7.2)使22Na进入脑区和脑脊液的速率降低25%,而注射NH4Cl产生的轻度酸中毒(pH 7.3)使脑摄取率降低18%,但脑脊液摄取率仅降低10%。与HCl酸中毒一样,氨氯吡咪使进入脑和脑脊液的转运降低22%。乙酰唑胺对22Na进入顶叶皮质的穿透率无影响,但进入脑脊液的速率减慢30%。由于当示踪剂摄取时间小于30分钟时,22Na进入皮质区域主要是示踪剂跨脑毛细血管的移动,结果表明代谢性酸中毒和氨氯吡咪均会降低脑毛细血管以及脉络丛处的Na+通透性。另一方面,乙酰唑胺仅改变Na+跨脉络膜上皮的移动。