Evidence that inositol 1-phosphate in brain of lithium-treated rats results mainly from phosphatidylinositol metabolism
- PMID: 3036092
- PMCID: PMC1147736
- DOI: 10.1042/bj2420517
Evidence that inositol 1-phosphate in brain of lithium-treated rats results mainly from phosphatidylinositol metabolism
Abstract
In cerebral cortex of rats treated with increasing doses of LiCl, the relative concentrations of Ins(1)P, Ins(4)P and Ins(5)P (when InsP is a myo-inositol phosphate) are approx. 10:1:0.2 at all doses. In rats treated with LiCl followed by increasing doses of pilocarpine a similar relationship occurs. myo-Inositol-1-phosphatase (InsP1ase) from bovine brain hydrolyses Ins(1)P, Ins(4)P and Ins(5)P at comparable rates, and these substrates have similar Km values. The hydrolysis of Ins(4)P is inhibited by Li+ to a greater degree than is hydrolysis of Ins(1)P and Ins(5)P. D-Ins(1,4,5)P3 and D-Ins(1,4)P2 are neither substrates nor inhibitors of InsP1ase. A dialysed high-speed supernatant of rat brain showed a greater rate of hydrolysis of Ins(1)P than of D-Ins(1,4)P2 and a lower sensitivity of the bisphosphate hydrolysis to LiCl, as compared with the monophosphate. That enzyme preparation produced Ins(4)P at a greater rate than Ins(1)P when D-Ins(1,4)P2 was the substrate. The amount of D-Ins(3)P [i.e. L-Ins(1)P, possibly from D-Ins(1,3,4)P3] is only 11% of that of D-Ins(1)P on stimulation with pilocarpine in the presence of Li+. DL-Ins(1,4)P2 was hydrolysed by InsP1ase to the extent of about 50%; both Ins(4)P and Ins(1)P are products, the former being produced more rapidly than the latter; apparently L-Ins(1,4)P2 is a substrate for InsP1ase. Li+, but not Ins(2)P, inhibited the hydrolysis of L-Ins(1,4)P2. The following were neither substrates nor inhibitors of InsP1ase; Ins(1,6)P2, Ins(1,2)P2, Ins(1,2,5,6)P4, Ins(1,2,4,5,6)P5, Ins(1,3,4,5,6)P5 and phytic acid. myo-Inositol 1,2-cyclic phosphate was neither substrate nor inhibitor of InsP1ase. We conclude that the 10-fold greater tissue contents of Ins(1)P relative to Ins(4)P in both stimulated and non-stimulated rat brain in vivo are the consequence of a much larger amount of PtdIns metabolism than polyphosphoinositide metabolism under these conditions.
Similar articles
-
The dephosphorylation pathway of D-myo-inositol 1,3,4,5-tetrakisphosphate in rat brain.Biochem J. 1987 Nov 1;247(3):635-9. doi: 10.1042/bj2470635. Biochem J. 1987. PMID: 2827634 Free PMC article.
-
Enzymic dephosphorylation of D-myo-inositol 1,4-bisphosphate in rat brain.Biochem J. 1987 Feb 15;242(1):193-8. doi: 10.1042/bj2420193. Biochem J. 1987. PMID: 3036085 Free PMC article.
-
Angiotensin-stimulated production of inositol trisphosphate isomers and rapid metabolism through inositol 4-monophosphate in adrenal glomerulosa cells.Proc Natl Acad Sci U S A. 1986 Dec;83(24):9323-7. doi: 10.1073/pnas.83.24.9323. Proc Natl Acad Sci U S A. 1986. PMID: 3025836 Free PMC article.
-
Toward a crystal-clear view of lithium's site of action.Proc Natl Acad Sci U S A. 1994 Jun 21;91(13):5738-9. doi: 10.1073/pnas.91.13.5738. Proc Natl Acad Sci U S A. 1994. PMID: 8016061 Free PMC article. Review. No abstract available.
-
Polyphosphoinositide metabolism in excitable membranes. Review.Biosci Rep. 1983 Oct;3(10):887-904. doi: 10.1007/BF01140658. Biosci Rep. 1983. PMID: 6317077 Review. No abstract available.
Cited by
-
Inhibition of agonist-stimulated inositol lipid metabolism by the anticonvulsant carbamazepine in rat hippocampus.Br J Pharmacol. 1989 Oct;98(2):581-9. doi: 10.1111/j.1476-5381.1989.tb12632.x. Br J Pharmacol. 1989. PMID: 2555014 Free PMC article.
-
Lithium-induced decrease of brain inositol and increase of brain inositol-1-phosphate is transient.Neurochem Res. 1991 Aug;16(8):905-11. doi: 10.1007/BF00965540. Neurochem Res. 1991. PMID: 1664916
-
The purification and properties of myo-inositol monophosphatase from bovine brain.Biochem J. 1988 Feb 1;249(3):883-9. doi: 10.1042/bj2490883. Biochem J. 1988. PMID: 2833231 Free PMC article.
-
Two G-proteins act in series to control stimulus-secretion coupling in mast cells: use of neomycin to distinguish between G-proteins controlling polyphosphoinositide phosphodiesterase and exocytosis.J Cell Biol. 1987 Dec;105(6 Pt 1):2745-50. doi: 10.1083/jcb.105.6.2745. J Cell Biol. 1987. PMID: 2447099 Free PMC article.
-
Subcellular localization of the enzymes that dephosphorylate myo-inositol polyphosphates in human platelets.Biochem J. 1988 Nov 1;255(3):795-800. doi: 10.1042/bj2550795. Biochem J. 1988. PMID: 2850797 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous