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Publication : Multiple hypothalamic cell populations encoding distinct visual information.

First Author  Brown TM Year  2011
Journal  J Physiol Volume  589
Issue  Pt 5 Pages  1173-94
PubMed ID  21224225 Mgi Jnum  J:183136
Mgi Id  MGI:5317520 Doi  10.1113/jphysiol.2010.199877
Citation  Brown TM, et al. (2011) Multiple hypothalamic cell populations encoding distinct visual information. J Physiol 589(Pt 5):1173-94
abstractText  Environmental illumination profoundly influences mammalian physiology and behaviour through actions on a master circadian oscillator in the suprachiasmatic nuclei (SCN) and other hypothalamic nuclei. The retinal and central mechanisms that shape daily patterns of light-evoked and spontaneous activity in this network of hypothalamic cells are still largely unclear. Similarly, the exact nature of the sensory information conveyed by such cells is unresolved. Here we set out to address these issues, through multielectrode recordings from the hypothalamus of red cone knockin mice (Opn1mwR). With this powerful mouse model, the photoreceptive origins of any response can be readily identified on the basis of their relative sensitivity to short and long wavelength light. Our experiments revealed that the firing pattern of many hypothalamic cells was influenced by changes in light levels and/or according to the steady state level of illumination. These 'contrast' and 'irradiance' responses were driven primarily by cone and melanopsin photoreceptors respectively, with rods exhibiting a much more subtle influence. Individual hypothalamic neurons differentially sampled from these information streams, giving rise to four distinct response types. The most common response phenotype in the SCN itself was sustained activation. Cells with this behaviour responded to all three photoreceptor classes in a manner consistent with their distinct contributions to circadian photoentrainment. These 'sustained' cells were also unique in our sample in expressing circadian firing patterns with highest activity during the mid projected day. Surprisingly, we also found a minority of SCN neurons that lacked the melanopsin-derived irradiance signal and responded only to light transitions, allowing for the possibility that rod-cone contrast signals may be routed to SCN output targets without influencing neighbouring circadian oscillators. Finally, an array of cells extending throughout the periventricular hypothalamus and ventral thalamus were excited or inhibited solely according to the activity of melanopsin. These cells appeared to convey a filtered version of the visual signal, suitable for modulating physiology/behaviour purely according to environmental irradiance. In summary, these findings reveal unexpectedly widespread hypothalamic cell populations encoding distinct qualities of visual information.
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