Abstract
Transient receptor potential vanilloid 4 (TRPV4), a cation channel responsive to hypotonicity, can also be activated by warm temperatures. Moreover, TRPV4-/- mice reportedly exhibit deficits in inflammation-induced thermal hyperalgesia. However, it is unknown whether TRPV4 or related transient receptor potential channels account for warmth perception under injury-free conditions. We therefore investigated the contribution of TRPV4 to thermosensation and thermoregulation in vivo. On a thermal gradient, TRPV4-/- mice selected warmer floor temperatures than wild-type littermates. In addition, whereas wild-type mice failed to discriminate between floor temperatures of 30 and 34 degrees C, TRPV4-/- mice exhibited a strong preference for 34 degrees C. TRPV4-/- mice also exhibited prolonged withdrawal latencies during acute tail heating. TRPV4-/- and wild-type mice exhibited similar changes in behavior on a thermal gradient after paw inflammation. Circadian body temperature fluctuations and thermoregulation in a warm environment were also indistinguishable between genotypes. These results demonstrate that TRPV4 is required for normal thermal responsiveness in vivo.
MeSH Terms
Animals
Arthritis, Experimental/physiopathology,psychology
Body Temperature Regulation
Cation Transport Proteins/deficiency,genetics,physiology
Circadian Rhythm
Freund's Adjuvant/toxicity
Genotype
Hot Temperature
Housing, Animal
Ion Channels/deficiency,genetics,physiology
Male
Mice
Mice, Inbred C57BL
Mice, Knockout
Perceptual Disorders/genetics,physiopathology
Phenotype
Reaction Time
TRPV Cation Channels
Chemicals
Cation Transport Proteins
Ion Channels
TRPV Cation Channels
Trpv4 protein, mouse
Freund's Adjuvant
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Lee Hyosang
Department of Biological Chemistry, Johns Hopkins School of Medicine, Baltimore, Maryland 21205, USA.
Iida Tohko
Mizuno Atsuko
Suzuki Makoto
Caterina Michael J
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