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@ARTICLE{Herold:14230,
      author       = {Herold, C. and Palomero-Gallagher, N. and Hellmann, B. and
                      Kröner, S. and Theiss, C. and Güntükün, O. and Zilles,
                      K.},
      title        = {{T}he receptor architecture of the pigeons' nidopallium
                      caudolaterale: an avian analogue to the mammalian prefrontal
                      cortex},
      journal      = {Brain structure $\&$ function},
      volume       = {216},
      issn         = {1863-2653},
      address      = {Berlin},
      publisher    = {Springer},
      reportid     = {PreJuSER-14230},
      pages        = {239 - 254},
      year         = {2011},
      note         = {Supported by a grant from the BMBF through the Bernstein
                      Focus Group "Varying Tunes'' to O.G.},
      abstract     = {The avian nidopallium caudolaterale is a multimodal area in
                      the caudal telencephalon that is apparently not homologous
                      to the mammalian prefrontal cortex but serves comparable
                      functions. Here we analyzed binding-site densities of
                      glutamatergic AMPA, NMDA and kainate receptors, GABAergic
                      GABA(A), muscarinic M(1), M(2) and nicotinic (nACh)
                      receptors, noradrenergic α(1) and α(2), serotonergic
                      5-HT(1A) and dopaminergic D(1)-like receptors using
                      quantitative in vitro receptor autoradiography. We compared
                      the receptor architecture of the pigeons' nidopallial
                      structures, in particular the NCL, with cortical areas Fr2
                      and Cg1 in rats and prefrontal area BA10 in humans. Our
                      results confirmed that the relative ratios of multiple
                      receptor densities across different nidopallial structures
                      (their "receptor fingerprints") were very similar in shape;
                      however, the absolute binding densities (the "size" of the
                      fingerprints) differed significantly. This finding enables a
                      delineation of the avian NCL from surrounding structures and
                      a further parcellation into a medial and a lateral part as
                      revealed by differences in densities of nACh, M(2), kainate,
                      and 5-HT(1A) receptors. Comparisons of the NCL with the rat
                      and human frontal structures showed differences in the
                      receptor distribution, particularly of the glutamate
                      receptors, but also revealed highly conserved features like
                      the identical densities of GABA(A), M(2), nACh and D(1)-like
                      receptors. Assuming a convergent evolution of avian and
                      mammalian prefrontal areas, our results support the
                      hypothesis that specific neurochemical traits provide the
                      molecular background for higher order processes such as
                      executive functions. The differences in glutamate receptor
                      distributions may reflect species-specific adaptations.},
      keywords     = {Animals / Autoradiography / Columbidae: anatomy $\&$
                      histology / Columbidae: metabolism / Densitometry / Humans /
                      Image Processing, Computer-Assisted / Rats / Receptor,
                      Muscarinic M1: metabolism / Receptor, Muscarinic M2:
                      metabolism / Receptor, Serotonin, 5-HT1A: metabolism /
                      Receptors, AMPA: metabolism / Receptors, Adrenergic:
                      metabolism / Receptors, Dopamine D1: metabolism / Receptors,
                      GABA-A: metabolism / Receptors, Kainic Acid: metabolism /
                      Receptors, N-Methyl-D-Aspartate: metabolism / Receptors,
                      Neurotransmitter: metabolism / Receptors, Nicotinic:
                      metabolism / Species Specificity / Telencephalon: anatomy
                      $\&$ histology / Telencephalon: metabolism / Receptor,
                      Muscarinic M1 (NLM Chemicals) / Receptor, Muscarinic M2 (NLM
                      Chemicals) / Receptors, AMPA (NLM Chemicals) / Receptors,
                      Adrenergic (NLM Chemicals) / Receptors, Dopamine D1 (NLM
                      Chemicals) / Receptors, GABA-A (NLM Chemicals) / Receptors,
                      Kainic Acid (NLM Chemicals) / Receptors,
                      N-Methyl-D-Aspartate (NLM Chemicals) / Receptors,
                      Neurotransmitter (NLM Chemicals) / Receptors, Nicotinic (NLM
                      Chemicals) / Receptor, Serotonin, 5-HT1A (NLM Chemicals) / J
                      (WoSType)},
      cin          = {INM-2},
      ddc          = {610},
      cid          = {I:(DE-Juel1)INM-2-20090406},
      pnm          = {Funktion und Dysfunktion des Nervensystems (FUEK409) /
                      89571 - Connectivity and Activity (POF2-89571)},
      pid          = {G:(DE-Juel1)FUEK409 / G:(DE-HGF)POF2-89571},
      shelfmark    = {Anatomy $\&$ Morphology / Neurosciences},
      typ          = {PUB:(DE-HGF)16},
      pubmed       = {pmid:21293877},
      UT           = {WOS:000293924300007},
      doi          = {10.1007/s00429-011-0301-5},
      url          = {https://juser.fz-juelich.de/record/14230},
}