Transient Receptor Potential Ion Channels Control Thermoregulatory Behaviour in Reptiles

Biological functions are governed by thermodynamics, and animals regulate their body temperature to optimise cellular performance and to avoid harmful extremes. The capacity to sense environmental and internal temperatures is a prerequisite for the evolution of thermoregulation. However, the mechanisms that enable ectothermic vertebrates to sense heat remain unknown. The recently discovered thermal characteristics of transient receptor potential ion channels (TRP) render these proteins suitable to act as temperature sensors. Here we test the hypothesis that TRPs are present in reptiles and function to control thermoregulatory behaviour. We show that the hot-sensing TRPV1 is expressed in a crocodile (Crocodylus porosus), an agamid (Amphibolurus muricatus) and a scincid (Pseudemoia entrecasteauxii) lizard, as well as in the quail and zebrafinch (Coturnix chinensis and Poephila guttata). The TRPV1 genes from all reptiles form a unique clade that is delineated from the mammalian and the ancestral Xenopus sequences by an insertion of two amino acids. TRPV1 and the cool-sensing TRPM8 are expressed in liver, muscle (transversospinalis complex), and heart tissues of the crocodile, and have the potential to act as internal thermometer and as external temperatures sensors. Inhibition of TRPV1 and TRPM8 in C. porosus abolishes the typically reptilian shuttling behaviour between cooling and heating environments, and leads to significantly altered body temperature patterns. Our results provide the proximate mechanism of thermal selection in terrestrial ectotherms, which heralds a fundamental change in interpretation, because TRPs provide the mechanism for a tissue-specific input into the animals' thermoregulatory response

Juvenile ribbontail stingray, Taeniura lymma (ForsskAyenl, 1775) (Chondrichthyes, Dasyatidae), demonstrate a unique suite of physiological adaptations to survive hyperthermic nursery conditions

Juvenile ribbontail stingrays, Taeniura lymma (Forsskål, 1775) of the tropical West Pacific inhabit mangal and seagrass nurseries that often experience rapid and extreme increases in water temperature. We hypothesized that juvenile rays possess a thermal strategy similar to other hyperthermic specialists, in which fish prefer high temperatures, are always prepared for thermal extremes regardless of previous thermal history, and exhibit low metabolic thermal sensitivity. Critical thermal methodology was used to determine the thermal niche, and a thermal gradient used to estimate stingray final preferendum. Temperature quotients (Q₁₀) were calculated from metabolic rates determined at three temperatures using flow-through respirometry. As predicted, juvenile rays showed a relatively small thermal niche dominated by intrinsic tolerance with limited capacity for acclimation. Thermal preference values were higher than those reported for other elasmobranch species. Interestingly, the temperature quotient for juvenile rays was higher than expected, suggesting that these fish may have the ability to exploit the thermal heterogeneity in their environment. Temperature likely acts as a directing factor in this species, separating warm tolerant juveniles from adults living in deeper, cooler waters