Polyamine transport, accumulation, and release in brain
- PMID: 12558981
- DOI: 10.1046/j.1471-4159.2003.01558.x
Polyamine transport, accumulation, and release in brain
Abstract
Cycling of polyamines (spermine and spermidine) in the brain was examined by measuring polyamine transport in synaptic vesicles, synaptosomes and glial cells, and the release of spermine from hippocampal slices. It was found that membrane potential-dependent polyamine transport systems exist in synaptosomes and glial cells, and a proton gradient-dependent polyamine transport system exists in synaptic vesicles. The glial cell transporter had high affinities for both spermine and spermidine, whereas the transporters in synaptosomes and synaptic vesicles had a much higher affinity for spermine than for spermidine. Polyamine transport by synaptosomes was inhibited by putrescine, agmatine, histidine, and histamine. Transport by glial cells was also inhibited by these four compounds and additionally by norepinephrine. On the other hand, polyamine transport by synaptic vesicles was inhibited only by putrescine and histamine. These results suggest that the polyamine transporters present in glial cells, neurons, and synaptic vesicles each have different properties and are, presumably, different molecular entities. Spermine was found to be accumulated in synaptic vesicles and was released from rat hippocampal slices by depolarization using a high concentration of KCl. Polyamines, in particular spermine, may function as neuromodulators in the brain.
Similar articles
-
Polyamine uptake, binding and release in rat brain.Eur J Pharmacol. 1991 Jan 25;193(1):41-6. doi: 10.1016/0014-2999(91)90198-y. Eur J Pharmacol. 1991. PMID: 2050191
-
Polyamine uptake across the basolateral membrane of the enterocyte is mediated by a high-affinity carrier: a study using isolated basolateral membrane vesicles.Digestion. 1998;59(1):60-8. doi: 10.1159/000007468. Digestion. 1998. PMID: 9468100
-
Polyamine catabolism is enhanced after traumatic brain injury.J Neurotrauma. 2010 Mar;27(3):515-25. doi: 10.1089/neu.2009.1097. J Neurotrauma. 2010. PMID: 19968558 Free PMC article.
-
Polyamine metabolism.Digestion. 1990;46 Suppl 2:319-30. doi: 10.1159/000200405. Digestion. 1990. PMID: 2262065 Review.
-
Catabolism of polyamines.Amino Acids. 2004 Jun;26(3):217-33. doi: 10.1007/s00726-004-0070-z. Epub 2004 Apr 20. Amino Acids. 2004. PMID: 15221502 Review.
Cited by
-
Targets of polyamine dysregulation in major depression and suicide: Activity-dependent feedback, excitability, and neurotransmission.Neurosci Biobehav Rev. 2016 Jul;66:80-91. doi: 10.1016/j.neubiorev.2016.04.010. Epub 2016 Apr 22. Neurosci Biobehav Rev. 2016. PMID: 27108532 Free PMC article. Review.
-
A New Transgenic Mouse Model for Studying the Neurotoxicity of Spermine Oxidase Dosage in the Response to Excitotoxic Injury.PLoS One. 2013 Jun 19;8(6):e64810. doi: 10.1371/journal.pone.0064810. Print 2013. PLoS One. 2013. PMID: 23840306 Free PMC article.
-
Transport of polyamines in Drosophila S2 cells: kinetics, pharmacology and dependence on the plasma membrane proton gradient.Biochem J. 2006 Jan 15;393(Pt 2):583-9. doi: 10.1042/BJ20050981. Biochem J. 2006. PMID: 16248856 Free PMC article.
-
Myosin Va interacts with the exosomal protein spermine synthase.Biosci Rep. 2019 Mar 1;39(3):BSR20182189. doi: 10.1042/BSR20182189. Print 2019 Mar 29. Biosci Rep. 2019. PMID: 30733278 Free PMC article.
-
Ablation of polyamine catabolic enzymes provokes Purkinje cell damage, neuroinflammation, and severe ataxia.J Neuroinflammation. 2020 Oct 14;17(1):301. doi: 10.1186/s12974-020-01955-6. J Neuroinflammation. 2020. PMID: 33054763 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources