2014
DOI: 10.1016/j.neuroscience.2013.12.015
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Colocalization pattern of calbindin and cocaine- and amphetamine-regulated transcript in the mammillary body–anterior thalamic nuclei axis of the guinea pig

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Cited by 12 publications
(9 citation statements)
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“…Interestingly, and in stark contrast to our Nts -cre results, we observed highly specific labeling of the AV subdivision of the ATN, while sparing the AM and AD. These data are consistent with immunohistochemical evidence in guinea pig suggesting that CART (encoded by Cartpt ) and calbindin (encoded by Calb1 ) are co-localized in the ML region of the MB and calbindin-immunoreactive fibers are concentrated in the AV subdivision of the ATN ( Żakowski et al, 2014 ). Taken together, these anterograde tracing data suggest that not only are molecularly-defined subpopulations of MB neurons highly segregated within the anatomical subdivisions of the MB (MnM, MM, ML, and LM), but these subpopulations appear to project to distinct domains within the ATN, consistent with previous anterograde and retrograde tracing data without genetic specificity ( Aggleton et al, 2010 ; Shibata, 1992 ; Jankowski et al, 2013 ; Bubb et al, 2017 ; Seki and Zyo, 1984 ; Hayakawa and Zyo, 1989 ; Wright et al, 2013 ).…”
Section: Resultssupporting
confidence: 91%
“…Interestingly, and in stark contrast to our Nts -cre results, we observed highly specific labeling of the AV subdivision of the ATN, while sparing the AM and AD. These data are consistent with immunohistochemical evidence in guinea pig suggesting that CART (encoded by Cartpt ) and calbindin (encoded by Calb1 ) are co-localized in the ML region of the MB and calbindin-immunoreactive fibers are concentrated in the AV subdivision of the ATN ( Żakowski et al, 2014 ). Taken together, these anterograde tracing data suggest that not only are molecularly-defined subpopulations of MB neurons highly segregated within the anatomical subdivisions of the MB (MnM, MM, ML, and LM), but these subpopulations appear to project to distinct domains within the ATN, consistent with previous anterograde and retrograde tracing data without genetic specificity ( Aggleton et al, 2010 ; Shibata, 1992 ; Jankowski et al, 2013 ; Bubb et al, 2017 ; Seki and Zyo, 1984 ; Hayakawa and Zyo, 1989 ; Wright et al, 2013 ).…”
Section: Resultssupporting
confidence: 91%
“…a combination of intrinsic excitation (unit bursting) and extrinsic inhibition (parvalbumineric/GABAergic input) is thought to be one mechanism through which network theta activity in other theta-generating circuitry is generated ( Colgin, 2013 ; Hu et al, 2002 ; Hutcheon and Yarom, 2000 ; Stark et al, 2013 ). Accordingly, the medial MBs express genes promoting rhythmic firing behaviour such as T-type calcium channel receptor subunits ( Talley et al, 1999 ) as well as various calcium binding proteins, including parvalbumin, calbindin, calretinin and hippocalcin ( Bernstein et al, 2007 ; Celio, 1990 ; Fortin and Parent, 1997 ; Paterlini et al, 2000 ; Zakowski et al, 2014 ). In addition, the medial MBs are also subject to diverse neuromodulatory influences, which are likely to support oscillatory activity and, more broadly, their role in memory.…”
Section: Electrophysiological Propertiesmentioning
confidence: 99%
“…CB and PV serve as markers of postnatal stages during development of the guinea pig anterior thalamic and septum, respectively (Zakowski et al, ; Hermanowicz‐Sobieraj and Robak, ). These proteins precisely mark also two functionally differentiated subsystems within the mammillary body‐anterior thalamic nuclei system (Zakowski et al, ). Although CB, CR, and PV were used as excellent markers of important cell populations in multiple brain regions, still, little is known about populations expressing these proteins in the preoptic area of the hypothalamus.…”
Section: Introductionmentioning
confidence: 99%