Literature DB >> 3612135

Postnatal development of cholinergic enzymes and receptors in mouse brain.

E P Fiedler, M J Marks, A C Collins.   

Abstract

The developmental profiles for the cholinergic enzymes acetylcholinesterase and choline acetyltransferase, and the muscarinic and nicotinic receptors were determined in whole mouse brain. The enzyme activities (per milligram of protein) increased steadily from birth, reaching adult levels at 20 days of age. These increases were primarily due to increases in Vmax. Muscarinic receptor numbers, measured by [3H]quinuclidinyl benzilate binding, also increased from birth to 25 days of age. Brain nicotinic receptors were measured with the ligands L-[3H]nicotine and alpha-[125I]-bungarotoxin. Neonatal mouse brain had approximately twice the number of alpha-bungarotoxin binding sites found in adult mouse brain. Binding site numbers rose slightly until 10 days of age, after which they decreased to adult values, which were reached at 25 days of age. The nicotine binding site was found in neonatal brain at concentrations comparable to those at the alpha-bungarotoxin site followed by a steady decline in nicotine binding until adult values were reached. Thus, brain nicotinic and muscarinic systems develop in totally different fashions; the quantity of muscarinic receptors increases with age, while the quantity of nicotinic receptors decreases. It is conceivable that nicotinic receptors play an important role in directing the development of the cholinergic system.

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Year:  1987        PMID: 3612135     DOI: 10.1111/j.1471-4159.1987.tb00990.x

Source DB:  PubMed          Journal:  J Neurochem        ISSN: 0022-3042            Impact factor:   5.372


  13 in total

1.  Developmental and regional quantitation of glycerophosphorylcholine phosphodiesterase activities in rat brain.

Authors:  J N Kanfer; D G McCartney
Journal:  Neurochem Res       Date:  1988-09       Impact factor: 3.996

2.  Pharmacology, distribution and development of muscarinic acetylcholine receptor subtypes in the optic tectum of Rana pipiens.

Authors:  C M Butt; J R Pauly; L H Wilkins; L P Dwoskin; E A Debski
Journal:  Neuroscience       Date:  2001       Impact factor: 3.590

3.  Dual recombinase fate mapping reveals a transient cholinergic phenotype in multiple populations of developing glutamatergic neurons.

Authors:  Nailyam Nasirova; Lely A Quina; Ibis M Agosto-Marlin; Jan-Marino Ramirez; Evelyn K Lambe; Eric E Turner
Journal:  J Comp Neurol       Date:  2019-08-22       Impact factor: 3.215

4.  Distribution and development of nicotinic acetylcholine receptor subtypes in the optic tectum of Rana pipiens.

Authors:  C M Butt; J R Pauly; E A Debski
Journal:  J Comp Neurol       Date:  2000-08-07       Impact factor: 3.215

5.  The developing cholinergic system as target for environmental toxicants, nicotine and polychlorinated biphenyls (PCBs): implications for neurotoxicological processes in mice.

Authors:  P Eriksson; E Ankarberg; H Viberg; A Fredriksson
Journal:  Neurotox Res       Date:  2001-01       Impact factor: 3.911

6.  Synchronized overproduction of neurotransmitter receptors in diverse regions of the primate cerebral cortex.

Authors:  M S Lidow; P S Goldman-Rakic; P Rakic
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-15       Impact factor: 11.205

7.  Nicotinic effects on excitatory field potentials recorded from the immature CA3 area of rat hippocampal slices.

Authors:  Caterina Psarropoulou; Melissa Boivin; Mark Anthony Laudadio
Journal:  Exp Brain Res       Date:  2003-07-26       Impact factor: 1.972

Review 8.  Thymopoietin, a thymic polypeptide, potently interacts at muscle and neuronal nicotinic alpha-bungarotoxin receptors.

Authors:  M Quik
Journal:  Mol Neurobiol       Date:  1992       Impact factor: 5.590

Review 9.  The dopamine hypothesis of schizophrenia: limbic interactions with serotonin and norepinephrine.

Authors:  J N Joyce
Journal:  Psychopharmacology (Berl)       Date:  1993       Impact factor: 4.530

10.  The development of the muscarinic acetylcholine receptor in normal and hyperphenylalaninemic rat cerebrum.

Authors:  K Matsuo; F A Hommes
Journal:  Neurochem Res       Date:  1988-09       Impact factor: 3.996

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