4.5 Article

Expression of m1-Type Muscarinic Acetylcholine Receptors by Parvalbumin-Immunoreactive Neurons in the Primary Visual Cortex: A Comparative Study of Rat, Guinea Pig, Ferret, Macaque, and Human

期刊

JOURNAL OF COMPARATIVE NEUROLOGY
卷 522, 期 5, 页码 986-1003

出版社

WILEY
DOI: 10.1002/cne.23456

关键词

striate cortex; neuromodulation; quantitative; anatomy; immunofluorescence; calcium-binding proteins; parvalbumin

资金

  1. National Institutes of Health [K99 MH-93567, R01 EY-021827]
  2. National Eye Institute [P30 EY19005]
  3. Gatsby Charitable Foundation

向作者/读者索取更多资源

Cholinergic neuromodulation is a candidate mechanism for aspects of arousal and attention in mammals. We have reported previously that cholinergic modulation in the primary visual cortex (V1) of the macaque monkey is strongly targeted toward GABAergic interneurons, and in particular that the vast majority of parvalbumin-immunoreactive (PV) neurons in macaque V1 express the m1-type (pirenzepine-sensitive, Gq-coupled) muscarinic ACh receptor (m1AChR). In contrast, previous physiological data indicates that PV neurons in rats rarely express pirenzepine-sensitive muscarinic AChRs. To examine further this apparent species difference in the cholinergic effectors for the primary visual cortex, we have conducted a comparative study of the expression of m1AChRs by PV neurons in V1 of rats, guinea pigs, ferrets, macaques, and humans. We visualize PV- and mAChR-immunoreactive somata by dual-immunofluorescence confocal microscopy and find that the species differences are profound; the vast majority (>75%) of PV-ir neurons in macaques, humans, and guinea pigs express m1AChRs. In contrast, in rats only approximate to 25% of the PV population is immunoreactive for m1AChRs. Our data reveal that while they do so much less frequently than in primates, PV neurons in rats do express Gq-coupled muscarinic AChRs, which appear to have gone undetected in the previous in vitro studies. Data such as these are critical in determining the species that represent adequate models for the capacity of the cholinergic system to modulate inhibition in the primate cortex. J. Comp. Neurol. 522:986-1003, 2014. (c) 2013 Wiley Periodicals, Inc.

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