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Peripheral sensory neurons expressing melanopsin respond to light

Matynia, Anna (author)
University of California, Los Angeles
Nguyen, Eileen (author)
University of California, Los Angeles
Sun, Xiaoping (author)
University of California, Los Angeles
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Blixt, Frank W. (author)
Lund University,Lunds universitet,Experimentell kärlforskning,Forskargrupper vid Lunds universitet,Experimental Vascular Research,Lund University Research Groups
Parikh, Sachin (author)
University of California, Los Angeles
Kessler, Jason (author)
University of California, Los Angeles
de Sevilla Müller, Luis Pérez (author)
University of California, Los Angeles
Habib, Samer (author)
University of California, Los Angeles
Kim, Paul (author)
University of California, Los Angeles
Wang, Zhe Z. (author)
University of California, Los Angeles
Rodriguez, Allen (author)
University of California, Los Angeles
Charles, Andrew (author)
University of California, Los Angeles
Nusinowitz, Steven (author)
University of California, Los Angeles
Edvinsson, Lars (author)
Lund University,Lunds universitet,Experimentell kärlforskning,Forskargrupper vid Lunds universitet,Experimental Vascular Research,Lund University Research Groups
Barnes, Steven (author)
University of California, Los Angeles,Dalhousie University
Brecha, Nicholas C. (author)
U.S. Department of Veterans Affairs,University of California, Los Angeles
Gorin, Michael B. (author)
University of California, Los Angeles
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 (creator_code:org_t)
2016-08-10
2016
English.
In: Frontiers in Neural Circuits. - : Frontiers Media SA. - 1662-5110. ; 10:AUG
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The ability of light to cause pain is paradoxical. The retina detects light but is devoid of nociceptors while the trigeminal sensory ganglia (TG) contain nociceptors but not photoreceptors. Melanopsin-expressing intrinsically photosensitive retinal ganglion cells (ipRGCs) are thought to mediate light-induced pain but recent evidence raises the possibility of an alternative light responsive pathway independent of the retina and optic nerve. Here, we show that melanopsin is expressed in both human and mouse TG neurons. In mice, they represent 3% of small TG neurons that are preferentially localized in the ophthalmic branch of the trigeminal nerve and are likely nociceptive C fibers and high-threshold mechanoreceptor Aδ fibers based on a strong size-function association. These isolated neurons respond to blue light stimuli with a delayed onset and sustained firing, similar to the melanopsin-dependent intrinsic photosensitivity observed in ipRGCs. Mice with severe bilateral optic nerve crush exhibit no light-induced responses including behavioral light aversion until treated with nitroglycerin, an inducer of migraine in people and migraine-like symptoms in mice. With nitroglycerin, these same mice with optic nerve crush exhibit significant light aversion. Furthermore, this retained light aversion remains dependent on melanopsin-expressing neurons. Our results demonstrate a novel light-responsive neural function independent of the optic nerve that may originate in the peripheral nervous system to provide the first direct mechanism for an alternative light detection pathway that influences motivated behavior.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Oftalmologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Ophthalmology (hsv//eng)

Keyword

Choroid
Cornea
IpRGC
Migraine
Optic nerve injury
Sensory ganglion

Publication and Content Type

art (subject category)
ref (subject category)

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