Myo-inositol transport in the central nervous system
- PMID: 1130554
- DOI: 10.1152/ajplegacy.1975.228.5.1510
Myo-inositol transport in the central nervous system
Abstract
Free myo-inositol (inositol) transport into the cerebrospinal fluid (CSF), brain, and choroid plexus and out of the cerebrospinal fluid was measured in rabbits. In vivo, inositol transport from blood into choroid plexus, CSF, and brain was saturable with an apparent affinity constant (K-t) of approximately 0.1 mM. The relative turnover of free inositol in choroid plexus (16 percent/h) was higher than in CSF 4percent/h) and brain (0.3percent/h) when meausred by tissue penetration of tracer [3-H]-labeled inositol injected into blood. However, the passage of tracer inositol was not greater than the passage of mannitol into brain when measured 15 s after a rapid injection of inositol and mannitol into the left common carotid artery. From the CSF, the clearance of inositol relative to inulin was saturable after the intraventricular injection of various concentrations of inositol and inulin. Moreover, a portion of the inositol cleared from the CSF entered brain by a saturable mechanism. In vitro, choroid plexuses, isolated from rabbits and incubated in artificial CSF, accumulated [3-H-labeled myo-inositol against a concentration gradient by a specific, active, saturable process with a K-t of 0.2 mM inositol. These results were interpreted as showing that the entry of inositol into the central nervous system from blood is regulated by a saturable transport system, and that the locus of this system may be, in part, in the choroid plexus.
Similar articles
-
Thiamine transport in the central nervous system.Am J Physiol. 1976 Apr;230(4):1101-7. doi: 10.1152/ajplegacy.1976.230.4.1101. Am J Physiol. 1976. PMID: 1267006
-
The transport of gentamicin in the choroid plexus and cerebrospinal fluid.J Pharmacol Exp Ther. 1975 Jul;194(1):82-8. J Pharmacol Exp Ther. 1975. PMID: 1151757
-
Riboflavin homeostasis in the central nervous system.J Neurochem. 1980 Jul;35(1):202-9. doi: 10.1111/j.1471-4159.1980.tb12507.x. J Neurochem. 1980. PMID: 7452254
-
Usefulness and limitation of primary cultured porcine choroid plexus epithelial cells as an in vitro model to study drug transport at the blood-CSF barrier.Adv Drug Deliv Rev. 2004 Oct 14;56(12):1859-73. doi: 10.1016/j.addr.2004.07.012. Adv Drug Deliv Rev. 2004. PMID: 15381337 Review.
-
Micronutrient and urate transport in choroid plexus and kidney: implications for drug therapy.Pharm Res. 2006 Nov;23(11):2515-24. doi: 10.1007/s11095-006-9091-5. Epub 2006 Oct 18. Pharm Res. 2006. PMID: 17048121 Review.
Cited by
-
Regulated inositol synthesis is critical for balanced metabolism and development in Drosophila melanogaster.Biol Open. 2021 Oct 15;10(10):bio058833. doi: 10.1242/bio.058833. Epub 2021 Oct 28. Biol Open. 2021. PMID: 34710213 Free PMC article.
-
Myo-inositol homeostasis in foetal rabbit lung.Biochem J. 1982 Jul 15;206(1):43-52. doi: 10.1042/bj2060043. Biochem J. 1982. PMID: 7126195 Free PMC article.
-
Two major inositol transporters and their role in cryptococcal virulence.Eukaryot Cell. 2011 May;10(5):618-28. doi: 10.1128/EC.00327-10. Epub 2011 Mar 11. Eukaryot Cell. 2011. PMID: 21398509 Free PMC article.
-
Polyol profiles in Down syndrome. myo-Inositol, specifically, is elevated in the cerebrospinal fluid.J Clin Invest. 1995 Feb;95(2):542-6. doi: 10.1172/JCI117696. J Clin Invest. 1995. PMID: 7860736 Free PMC article. Clinical Trial.
-
Restoration of brain myo-inositol levels in rats increases latency to lithium-pilocarpine seizures.Psychopharmacology (Berl). 1993;110(1-2):229-34. doi: 10.1007/BF02246978. Psychopharmacology (Berl). 1993. PMID: 7870890
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources