1990
DOI: 10.1002/cne.903000107
|View full text |Cite
|
Sign up to set email alerts
|

Distribution of cholecystokinin‐like‐immunoreactive neurons in the guinea pig forebrain

Abstract: The distribution of cholecystokinin (CCK)-immunoreactive nerve fibers and cell bodies was studied in the forebrain of control and colchicine-treated guinea pigs by using an antiserum directed against the carboxyterminus of CCK octapeptide (CCK-8) in the indirect immunoperoxidase technique. Virtually all forebrain areas examined contained immunoreactive nerve fibers. A dense innervation was visualized in; neocortical layers II-III, piriform cortex, the medial amygdala, the medial preoptic area, a circumventricu… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

2
18
0

Year Published

2010
2010
2017
2017

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 24 publications
(20 citation statements)
references
References 162 publications
2
18
0
Order By: Relevance
“…The specificity controls performed by immunocytochemistry and radioimmunoassay of the cholecystokinin (CCK) antiserum IS-15/8 show the expected crossreaction with gastrin (Ciofi and Tramu, 1990). CCK labeling is mainly found in large somata at the EPL/GL border (presumably in medium-sized tufted cells), as also reported using a mouse monoclonal antibody Kosaka and Kosaka, 2007b).…”
Section: Antibodies Characterizationsupporting
confidence: 65%
“…The specificity controls performed by immunocytochemistry and radioimmunoassay of the cholecystokinin (CCK) antiserum IS-15/8 show the expected crossreaction with gastrin (Ciofi and Tramu, 1990). CCK labeling is mainly found in large somata at the EPL/GL border (presumably in medium-sized tufted cells), as also reported using a mouse monoclonal antibody Kosaka and Kosaka, 2007b).…”
Section: Antibodies Characterizationsupporting
confidence: 65%
“…Labeling is abolished in the rodent brain by preadsorption with porcine galanin but not by porcine neuropeptide Y (NPY), GnRH, or vasopressin (Gasman et al, 1996;Ciofi and Tramu, unpublished observations Characterization by radioimmunoassay showed cross-reactivity with CCK-33 and gastrin but no cross-reactivity with substance P, Leu-or Met-enkephalin, b-endorphin, or FMRFamide (Studler et al, 1984). Immunocytochemical labeling is abolished in rodent brain by preadsorption with 10 À6 M CCK-8 and gastrin 1, but not by neurotensin, human growth hormone-releasing hormone (GHRH), porcine NPY, substance P, or leu-or Met-enkephalin (Ciofi and Tramu, 1990). The distribution of CCK-immunoreactive cell bodies reported here matches the mapping of CCK mRNA expression in mouse brain (Allen Institute Brain Atlas).…”
Section: Antibody Characterizationmentioning
confidence: 89%
“…The following antisera were used: anti-KP (#AC024, 1:5000, from A. Caraty, INRA, Nouzilly, France), anti-galanin (# IS-42; 1:2000, Interchim Cat# AP101500, RRID: AB_2314518), anti-CCK-8 (# IS-15/8 RRID: AB_2314186, 1:1000, from P. Ciofi, National Institute of Health and Medical Research, Bordeaux, France) and anti-tyrosine hydroxylase (TH) (#TYH, 1:1000; Aves Labs Inc., Tigard, OR, USA). The characterization and specificity of the primary antibodies have been published elsewhere (Ciofi and Tramu, 1990; Porteous et al, 2011), the pre-absorption of the antibodies or their omission from the staining resulted in immunonegative sections. Cy3-conjugated secondary antibodies (Jackson Immunoresearch Europe Ltd, Suffolk, UK) were diluted in PBS containing 2% NHS (1:500) and applied on the sections for 4 h at RT.…”
Section: Methodsmentioning
confidence: 99%