Parallel Postnatal Development of Choline Acetyltransferase Activity and Muscarinic Acetylcholine Receptors in the Rat Olfactory Bulb

: The development of cholinergic synapses in the rat olfactory bulb was investigated by measuring changes in the activity of choline acetyltransferase (ChAT; EC 2.3.1.6.), a presynaptic cholinergic marker, and in the concentration of muscarinic receptors, components of cholinoceptive membranes. Thre...

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Veröffentlicht in:Journal of neurochemistry 1986-03, Vol.46 (3), p.671-680
Hauptverfasser: Large, Thomas H., Lambert, Mary P., Gremillion, Maureen A., Klein, William L.
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creator Large, Thomas H.
Lambert, Mary P.
Gremillion, Maureen A.
Klein, William L.
description : The development of cholinergic synapses in the rat olfactory bulb was investigated by measuring changes in the activity of choline acetyltransferase (ChAT; EC 2.3.1.6.), a presynaptic cholinergic marker, and in the concentration of muscarinic receptors, components of cholinoceptive membranes. Three biochemical properties of the muscarinic system also were examined for possible differentiation: ligand binding, molecular weight, and isoelectric point. Receptors from embryonic (day 18), neonatal (postnatal day 3), and adult rat olfactory bulbs exhibited identical complex binding (nH= 0.45) of the agonist carbachol. For each age, the relative proportions of high‐affinity (Ki= 1.0 μM) and low‐affinity (Ki= 100 μM) binding states were 60% and 40%, respectively. The antagonist pirenzepine also bound to high‐affinity (Ki= 0.15 μM, RH= 70%) and low‐affinity (Ki= 2.0 μM, RL= 30%) sites in neonatal and adult rats. Sodium dodecyl sulfate/urea‐polyacrylamide gel electrophoresis of [3H]propyibenzilylcholine mustard‐labeled receptors from neonatal and adult rats showed a single electrophoretic form with an apparent molecular weight of 65,000. In contrast, analytical isoelectric focusing indicated high pI (4.50) and low pI (4.00) receptor forms were present. Neonatal rats contained approximately equal proportions of the two receptor forms, whereas adult rats contained mainly the low pI form, indicating that molecular alteration of the receptor population had occurred during development. Comparison of postnatal changes in acetylcholine receptors and ChAT activity showed a striking correlation between the development of cholinergic terminals and muscarinic receptors. Throughout the first postnatal week, ChAT activity remained at 5% of adult levels; activity began to rise on postnatal day 6 and gradually reached adult levels (56 ± 4 μnol of [3H]acetylcholine/h/g) during the fourth week. Similarly, muscarinic receptor concentration was low (30–50 fmol/mg) throughout the first week, began to rise at postnatal day 7; and reached 90% of adult levels (317 ± 17 fmol/mg) by the fourth week. In contrast, there was little increase in the concentration of nicotinic acetylcholine receptors (30 fmol/mg) during this period. The parallel postnatal development of ChAT activity and muscarinic receptors suggests the existence of factors that couple the differentiation of presynaptic cholinergic terminals and postsynaptic cholinoceptive elements.
doi_str_mv 10.1111/j.1471-4159.1986.tb13024.x
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Three biochemical properties of the muscarinic system also were examined for possible differentiation: ligand binding, molecular weight, and isoelectric point. Receptors from embryonic (day 18), neonatal (postnatal day 3), and adult rat olfactory bulbs exhibited identical complex binding (nH= 0.45) of the agonist carbachol. For each age, the relative proportions of high‐affinity (Ki= 1.0 μM) and low‐affinity (Ki= 100 μM) binding states were 60% and 40%, respectively. The antagonist pirenzepine also bound to high‐affinity (Ki= 0.15 μM, RH= 70%) and low‐affinity (Ki= 2.0 μM, RL= 30%) sites in neonatal and adult rats. Sodium dodecyl sulfate/urea‐polyacrylamide gel electrophoresis of [3H]propyibenzilylcholine mustard‐labeled receptors from neonatal and adult rats showed a single electrophoretic form with an apparent molecular weight of 65,000. In contrast, analytical isoelectric focusing indicated high pI (4.50) and low pI (4.00) receptor forms were present. Neonatal rats contained approximately equal proportions of the two receptor forms, whereas adult rats contained mainly the low pI form, indicating that molecular alteration of the receptor population had occurred during development. Comparison of postnatal changes in acetylcholine receptors and ChAT activity showed a striking correlation between the development of cholinergic terminals and muscarinic receptors. Throughout the first postnatal week, ChAT activity remained at 5% of adult levels; activity began to rise on postnatal day 6 and gradually reached adult levels (56 ± 4 μnol of [3H]acetylcholine/h/g) during the fourth week. Similarly, muscarinic receptor concentration was low (30–50 fmol/mg) throughout the first week, began to rise at postnatal day 7; and reached 90% of adult levels (317 ± 17 fmol/mg) by the fourth week. In contrast, there was little increase in the concentration of nicotinic acetylcholine receptors (30 fmol/mg) during this period. The parallel postnatal development of ChAT activity and muscarinic receptors suggests the existence of factors that couple the differentiation of presynaptic cholinergic terminals and postsynaptic cholinoceptive elements.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1111/j.1471-4159.1986.tb13024.x</identifier><identifier>PMID: 3754001</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>acetylcholine ; Animals ; Animals, Newborn - metabolism ; Benzodiazepinones - metabolism ; Binding, Competitive ; Biological and medical sciences ; choline acetyltransferase ; Choline O-Acetyltransferase - metabolism ; Diagonal band ; Electrophoresis, Polyacrylamide Gel ; Fundamental and applied biological sciences. Psychology ; Guanylyl Imidodiphosphate - pharmacology ; Isoelectric focusing ; Isoelectric Point ; Molecular Weight ; N-Methylscopolamine ; olfactory bulb ; Olfactory Bulb - embryology ; Olfactory Bulb - growth &amp; development ; Olfactory Bulb - metabolism ; Olfactory system and olfaction. Gustatory system and gustation ; Pirenzepine ; Posttransla‐tional modification ; Propylbenzilylcholine Mustard - metabolism ; Quinuclidinyl Benzilate - metabolism ; Radioligand Assay ; Rats ; Receptors, Muscarinic - drug effects ; Receptors, Muscarinic - metabolism ; Receptors, Nicotinic - metabolism ; Scopolamine Derivatives - metabolism ; Synaptogenesis ; Trophic factors ; Vertebrates: nervous system and sense organs</subject><ispartof>Journal of neurochemistry, 1986-03, Vol.46 (3), p.671-680</ispartof><rights>1986 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4291-f518a933e2e538cd7b12402897e0273093722b4e81de68d085cd31e7cc3e7b853</citedby><cites>FETCH-LOGICAL-c4291-f518a933e2e538cd7b12402897e0273093722b4e81de68d085cd31e7cc3e7b853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-4159.1986.tb13024.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-4159.1986.tb13024.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27931,27932,45581,45582</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=8801377$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3754001$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Large, Thomas H.</creatorcontrib><creatorcontrib>Lambert, Mary P.</creatorcontrib><creatorcontrib>Gremillion, Maureen A.</creatorcontrib><creatorcontrib>Klein, William L.</creatorcontrib><title>Parallel Postnatal Development of Choline Acetyltransferase Activity and Muscarinic Acetylcholine Receptors in the Rat Olfactory Bulb</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>: The development of cholinergic synapses in the rat olfactory bulb was investigated by measuring changes in the activity of choline acetyltransferase (ChAT; EC 2.3.1.6.), a presynaptic cholinergic marker, and in the concentration of muscarinic receptors, components of cholinoceptive membranes. Three biochemical properties of the muscarinic system also were examined for possible differentiation: ligand binding, molecular weight, and isoelectric point. Receptors from embryonic (day 18), neonatal (postnatal day 3), and adult rat olfactory bulbs exhibited identical complex binding (nH= 0.45) of the agonist carbachol. For each age, the relative proportions of high‐affinity (Ki= 1.0 μM) and low‐affinity (Ki= 100 μM) binding states were 60% and 40%, respectively. The antagonist pirenzepine also bound to high‐affinity (Ki= 0.15 μM, RH= 70%) and low‐affinity (Ki= 2.0 μM, RL= 30%) sites in neonatal and adult rats. Sodium dodecyl sulfate/urea‐polyacrylamide gel electrophoresis of [3H]propyibenzilylcholine mustard‐labeled receptors from neonatal and adult rats showed a single electrophoretic form with an apparent molecular weight of 65,000. In contrast, analytical isoelectric focusing indicated high pI (4.50) and low pI (4.00) receptor forms were present. Neonatal rats contained approximately equal proportions of the two receptor forms, whereas adult rats contained mainly the low pI form, indicating that molecular alteration of the receptor population had occurred during development. Comparison of postnatal changes in acetylcholine receptors and ChAT activity showed a striking correlation between the development of cholinergic terminals and muscarinic receptors. Throughout the first postnatal week, ChAT activity remained at 5% of adult levels; activity began to rise on postnatal day 6 and gradually reached adult levels (56 ± 4 μnol of [3H]acetylcholine/h/g) during the fourth week. Similarly, muscarinic receptor concentration was low (30–50 fmol/mg) throughout the first week, began to rise at postnatal day 7; and reached 90% of adult levels (317 ± 17 fmol/mg) by the fourth week. In contrast, there was little increase in the concentration of nicotinic acetylcholine receptors (30 fmol/mg) during this period. The parallel postnatal development of ChAT activity and muscarinic receptors suggests the existence of factors that couple the differentiation of presynaptic cholinergic terminals and postsynaptic cholinoceptive elements.</description><subject>acetylcholine</subject><subject>Animals</subject><subject>Animals, Newborn - metabolism</subject><subject>Benzodiazepinones - metabolism</subject><subject>Binding, Competitive</subject><subject>Biological and medical sciences</subject><subject>choline acetyltransferase</subject><subject>Choline O-Acetyltransferase - metabolism</subject><subject>Diagonal band</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guanylyl Imidodiphosphate - pharmacology</subject><subject>Isoelectric focusing</subject><subject>Isoelectric Point</subject><subject>Molecular Weight</subject><subject>N-Methylscopolamine</subject><subject>olfactory bulb</subject><subject>Olfactory Bulb - embryology</subject><subject>Olfactory Bulb - growth &amp; development</subject><subject>Olfactory Bulb - metabolism</subject><subject>Olfactory system and olfaction. Gustatory system and gustation</subject><subject>Pirenzepine</subject><subject>Posttransla‐tional modification</subject><subject>Propylbenzilylcholine Mustard - metabolism</subject><subject>Quinuclidinyl Benzilate - metabolism</subject><subject>Radioligand Assay</subject><subject>Rats</subject><subject>Receptors, Muscarinic - drug effects</subject><subject>Receptors, Muscarinic - metabolism</subject><subject>Receptors, Nicotinic - metabolism</subject><subject>Scopolamine Derivatives - metabolism</subject><subject>Synaptogenesis</subject><subject>Trophic factors</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkd1u1DAQhS0EKkvhEZAshLhL8F9ihwuksvyr0ArBteU4E9Urb7LYTmkegPfGYaO9RfjG8jnfzFhzEHpGSUnzebkrqZC0ELRqStqoukwt5YSJ8u4e2pys-2hDCGMFJ4I9RI9i3BFCa1HTM3TGZSXya4N-X5tgvAePr8eYBpOMx2_hFvx42MOQ8Njj7c3o3QD4wkKafQpmiD0EExcluVuXZmyGDn-ZojXBDc6upF3rvoGFQxpDxG7A6SYLJuEr3xubxRm_mXz7GD3ojY_wZL3P0Y_3775vPxaXVx8-bS8uCytYQ4u-oso0nAODiivbyZYyQZhqJBAmOWm4ZKwVoGgHteqIqmzHKUhrOchWVfwcvTj2PYTx5wQx6b2LFrw3A4xT1LKWrJI1-ydIBRdU_O346gjaMMYYoNeH4PYmzJoSvYSld3pJRC-J6CUsvYal73Lx03XK1O6hO5Wu6WT_-eqbvFvf59VbF0-YUpmRMmOvj9gv52H-jw_oz1-3taT8D1uvslI</recordid><startdate>198603</startdate><enddate>198603</enddate><creator>Large, Thomas H.</creator><creator>Lambert, Mary P.</creator><creator>Gremillion, Maureen A.</creator><creator>Klein, William L.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>198603</creationdate><title>Parallel Postnatal Development of Choline Acetyltransferase Activity and Muscarinic Acetylcholine Receptors in the Rat Olfactory Bulb</title><author>Large, Thomas H. ; Lambert, Mary P. ; Gremillion, Maureen A. ; Klein, William L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4291-f518a933e2e538cd7b12402897e0273093722b4e81de68d085cd31e7cc3e7b853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>acetylcholine</topic><topic>Animals</topic><topic>Animals, Newborn - metabolism</topic><topic>Benzodiazepinones - metabolism</topic><topic>Binding, Competitive</topic><topic>Biological and medical sciences</topic><topic>choline acetyltransferase</topic><topic>Choline O-Acetyltransferase - metabolism</topic><topic>Diagonal band</topic><topic>Electrophoresis, Polyacrylamide Gel</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Guanylyl Imidodiphosphate - pharmacology</topic><topic>Isoelectric focusing</topic><topic>Isoelectric Point</topic><topic>Molecular Weight</topic><topic>N-Methylscopolamine</topic><topic>olfactory bulb</topic><topic>Olfactory Bulb - embryology</topic><topic>Olfactory Bulb - growth &amp; development</topic><topic>Olfactory Bulb - metabolism</topic><topic>Olfactory system and olfaction. Gustatory system and gustation</topic><topic>Pirenzepine</topic><topic>Posttransla‐tional modification</topic><topic>Propylbenzilylcholine Mustard - metabolism</topic><topic>Quinuclidinyl Benzilate - metabolism</topic><topic>Radioligand Assay</topic><topic>Rats</topic><topic>Receptors, Muscarinic - drug effects</topic><topic>Receptors, Muscarinic - metabolism</topic><topic>Receptors, Nicotinic - metabolism</topic><topic>Scopolamine Derivatives - metabolism</topic><topic>Synaptogenesis</topic><topic>Trophic factors</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Large, Thomas H.</creatorcontrib><creatorcontrib>Lambert, Mary P.</creatorcontrib><creatorcontrib>Gremillion, Maureen A.</creatorcontrib><creatorcontrib>Klein, William L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Large, Thomas H.</au><au>Lambert, Mary P.</au><au>Gremillion, Maureen A.</au><au>Klein, William L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Parallel Postnatal Development of Choline Acetyltransferase Activity and Muscarinic Acetylcholine Receptors in the Rat Olfactory Bulb</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1986-03</date><risdate>1986</risdate><volume>46</volume><issue>3</issue><spage>671</spage><epage>680</epage><pages>671-680</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: The development of cholinergic synapses in the rat olfactory bulb was investigated by measuring changes in the activity of choline acetyltransferase (ChAT; EC 2.3.1.6.), a presynaptic cholinergic marker, and in the concentration of muscarinic receptors, components of cholinoceptive membranes. Three biochemical properties of the muscarinic system also were examined for possible differentiation: ligand binding, molecular weight, and isoelectric point. Receptors from embryonic (day 18), neonatal (postnatal day 3), and adult rat olfactory bulbs exhibited identical complex binding (nH= 0.45) of the agonist carbachol. For each age, the relative proportions of high‐affinity (Ki= 1.0 μM) and low‐affinity (Ki= 100 μM) binding states were 60% and 40%, respectively. The antagonist pirenzepine also bound to high‐affinity (Ki= 0.15 μM, RH= 70%) and low‐affinity (Ki= 2.0 μM, RL= 30%) sites in neonatal and adult rats. Sodium dodecyl sulfate/urea‐polyacrylamide gel electrophoresis of [3H]propyibenzilylcholine mustard‐labeled receptors from neonatal and adult rats showed a single electrophoretic form with an apparent molecular weight of 65,000. In contrast, analytical isoelectric focusing indicated high pI (4.50) and low pI (4.00) receptor forms were present. Neonatal rats contained approximately equal proportions of the two receptor forms, whereas adult rats contained mainly the low pI form, indicating that molecular alteration of the receptor population had occurred during development. Comparison of postnatal changes in acetylcholine receptors and ChAT activity showed a striking correlation between the development of cholinergic terminals and muscarinic receptors. Throughout the first postnatal week, ChAT activity remained at 5% of adult levels; activity began to rise on postnatal day 6 and gradually reached adult levels (56 ± 4 μnol of [3H]acetylcholine/h/g) during the fourth week. Similarly, muscarinic receptor concentration was low (30–50 fmol/mg) throughout the first week, began to rise at postnatal day 7; and reached 90% of adult levels (317 ± 17 fmol/mg) by the fourth week. In contrast, there was little increase in the concentration of nicotinic acetylcholine receptors (30 fmol/mg) during this period. The parallel postnatal development of ChAT activity and muscarinic receptors suggests the existence of factors that couple the differentiation of presynaptic cholinergic terminals and postsynaptic cholinoceptive elements.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>3754001</pmid><doi>10.1111/j.1471-4159.1986.tb13024.x</doi><tpages>10</tpages></addata></record>
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ispartof Journal of neurochemistry, 1986-03, Vol.46 (3), p.671-680
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1471-4159
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subjects acetylcholine
Animals
Animals, Newborn - metabolism
Benzodiazepinones - metabolism
Binding, Competitive
Biological and medical sciences
choline acetyltransferase
Choline O-Acetyltransferase - metabolism
Diagonal band
Electrophoresis, Polyacrylamide Gel
Fundamental and applied biological sciences. Psychology
Guanylyl Imidodiphosphate - pharmacology
Isoelectric focusing
Isoelectric Point
Molecular Weight
N-Methylscopolamine
olfactory bulb
Olfactory Bulb - embryology
Olfactory Bulb - growth & development
Olfactory Bulb - metabolism
Olfactory system and olfaction. Gustatory system and gustation
Pirenzepine
Posttransla‐tional modification
Propylbenzilylcholine Mustard - metabolism
Quinuclidinyl Benzilate - metabolism
Radioligand Assay
Rats
Receptors, Muscarinic - drug effects
Receptors, Muscarinic - metabolism
Receptors, Nicotinic - metabolism
Scopolamine Derivatives - metabolism
Synaptogenesis
Trophic factors
Vertebrates: nervous system and sense organs
title Parallel Postnatal Development of Choline Acetyltransferase Activity and Muscarinic Acetylcholine Receptors in the Rat Olfactory Bulb
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