1989
DOI: 10.1016/0167-0115(89)90251-6
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Ontogeny of the novel tachykinins neurokinin A, neurokinin B and neuropeptide K in the rat central nervous system

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Cited by 24 publications
(9 citation statements)
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“…and 5-HT systems in the brain has been obtained by using different methodological approaches such as fluorescence histochemistry, immunocytochemistry of enzymes, amine uptake, radioenzymatic assays, and HPLC (Pares-Herbute et al, 1989, and references cited therein). Similarly, isolated reports of the ontogenetic development of enkephalin and tachykinin neurons using immunocytochemistry or radioimmunoassay for the determination of peptide levels, ligand binding studies for receptors, and Northern blot analysis or in situ hybridization histochemistry for the determination of the abundance of peptide-encoding mRNAs are available (Bayon et al, 1979;Patey et al, 1980;Inagaki et al, 1982;Palmer et al, 1982;Pickel et al, 1982;Tsang et a]., 1982;McDowell and Kitchen, 1987;Schwartz and Simatov, 1988;Yoshikawa and Aizawa, 1988;Diez-Guerra et al, 1989;Tecott et al, 1989;Haverstick et al, 1990). The peptide measurements in the ontogenetic studies were by and large done with immunocytochemical methods, which have the advantage of demonstrating the topographical and structural distribution.…”
Section: General Considerationsmentioning
confidence: 99%
“…and 5-HT systems in the brain has been obtained by using different methodological approaches such as fluorescence histochemistry, immunocytochemistry of enzymes, amine uptake, radioenzymatic assays, and HPLC (Pares-Herbute et al, 1989, and references cited therein). Similarly, isolated reports of the ontogenetic development of enkephalin and tachykinin neurons using immunocytochemistry or radioimmunoassay for the determination of peptide levels, ligand binding studies for receptors, and Northern blot analysis or in situ hybridization histochemistry for the determination of the abundance of peptide-encoding mRNAs are available (Bayon et al, 1979;Patey et al, 1980;Inagaki et al, 1982;Palmer et al, 1982;Pickel et al, 1982;Tsang et a]., 1982;McDowell and Kitchen, 1987;Schwartz and Simatov, 1988;Yoshikawa and Aizawa, 1988;Diez-Guerra et al, 1989;Tecott et al, 1989;Haverstick et al, 1990). The peptide measurements in the ontogenetic studies were by and large done with immunocytochemical methods, which have the advantage of demonstrating the topographical and structural distribution.…”
Section: General Considerationsmentioning
confidence: 99%
“…Therefore these data suggest that unknown maturational factors selectively promote SP expression in growing neurons. Strikingly, tachykinins neurokinin A, neurokinin B, and neuropeptide K have the same ontogenic development as SP (Diez-Guerra et al, 1989). Two different genes encode for these tachykinins (Carter and Krause, 1990;Kotani et al, 1986).…”
Section: Discussionmentioning
confidence: 99%
“…The somatodendritic phenotypes of medium tachykinin neurons in feline neostriatum match tachykinin cells of unknown somatodendritic phenotypes commonly reported in mammals [1,2,3,6,7,8,9]. Principal and minor variants of medium spiny tachykinin neurons are identical to medium spiny neurons with unknown neuromodulator signatures shown by Golgi impregnation, which constitute approximately 95% of neurons in adult feline neostriatum [19].…”
Section: Discussionmentioning
confidence: 99%
“…In immature rats and cats, tachykinins show a pattern of early, progressive expression in numerous small to medium neurons in the neostriatum (caudate nucleus, putamen and, when separate, their intervening cell bridges) during middle and late fetal periods, prior to their perinatal establishment of significant synaptic connectivity via local axon collaterals or descending (i.e. striatonigral) axon projections [1,2]. The morphogenetic properties of these cells are largely uncharted, and their characterization is the first objective of the present study.…”
Section: Introductionmentioning
confidence: 99%