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Hypothalamic TRPV4 channels participate in the medial preoptic activation of warmth-defence responses in Wistar male rats

  • Neuroscience
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Abstract

Recently, we have described, in non-genetically modified rats, that peripheral transient receptor potential vanilloid-4 (TRPV4) channels are activated and trigger warmth-defence responses at ambient temperatures of 26–30 °C. Evidence points to the presence of TRPV4 in the medial preoptic area, a region described to be involved in the activation of thermoeffector pathways, including those involved in heat loss. Thus, we tested the hypothesis that TRPV4 in the medial preoptic area modulates thermoregulation under warm conditions. To this end, under two ambient temperatures (21 and 28 °C), body temperature was measured in rats following blockade of preoptic TRPV4 with two antagonists, HC-067047 and GSK 2193874. Oxygen consumption, heat loss index and preferred ambient temperature were also determined in order to assess thermoeffector activity. Antagonism of central TRPV4 caused an increase in body temperature in rats exposed to 28 °C, but not in those exposed to 21 °C. The body temperature increase at 28 °C was accompanied by an increase in oxygen consumption and an earlier reduction of the heat loss index. In behavioural experiments, control animals previously exposed to warm ambient temperatures (28–30 °C) for 2 h selected colder temperatures in a thermogradient compared to those injected with HC-067047. Our results support the idea that preoptic TRPV4 modulates thermoregulation in a warm environment by activating both autonomic and behavioural heat loss responses. Thus, according to the present study and to that published recently by our group, the activation of warmth-defence responses by TRPV4 seems to be dependent on the activity of both peripheral and central channels.

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References

  1. Aihara H, Okada Y, Tamaki N (2011) The effects of cooling and rewarming on the neuronal activity of pyramidal neurons in guinea pig hippocampal slices. Brain Res 893:36–45

    Article  Google Scholar 

  2. Almeida MC, Steiner AA, Branco LGS, Romanovsky AA (2006a) Cold-seeking behavior as a thermoregulatory strategy in systemic inflammation. Eur J Neurosci 23:3359–3367. https://doi.org/10.1111/j.1460-9568.2006.04854.x

    Article  PubMed  Google Scholar 

  3. Almeida MC, Steiner AA, Branco LGS, Romanovsky AA (2006b) Neural substrate of cold-seeking behavior in endotoxin shock. PLoS One 1(1):e1. https://doi.org/10.1371/journal.pone.0000001

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Bicego KC, Branco LGS (2002) Discrete electrolytic lesions of the preoptic area prevents LPS-induced behavioral fever in toads. J Exp Biol 205:3513–3518

    PubMed  Google Scholar 

  5. Blatteis CM (1998) Physiology and pathophysiology of temperature regulation. World Scentific, New Jersey

    Book  Google Scholar 

  6. Boulant JA (2000) Role of the preoptic-anterior hypothalamus in thermoregulation and fever. Clin Infect Dis 31:S157–S161

    Article  PubMed  Google Scholar 

  7. Boychuk CR, Zsombok A, Tasker JG, Smith BN (2013) Rapid glucocorticoid-induced activation of TRP and CB1 receptors causes biphasic modulation of glutamate release in gastric-related hypothalamic preautonomic neurons. Front Neurosci 7:3. https://doi.org/10.3389/fnins.2013.00003

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Caterina MJ (2007) Transient receptor potential ion channels as participants in thermosensation and thermoregulation. Am J Physiol Regul Integr Comp Physiol 292:R64–R76. https://doi.org/10.1152/ajpregu.00446.2006

    Article  CAS  PubMed  Google Scholar 

  9. Cheung M, Bao W, Behm DJ, Brooks CA, Bury MJ, Dowdell SE, Eidam HS, Fox RM, Goodman KB, Holt DA, Lee D, Roethke TJ, Willette RN, Xu X, Ye G, Thorneloe KS (2017) Discovery of GSK 2193874: an orally active, potent and selective blocker of transient receptor potential vanilloid 4. ACS Med Chem Lett 5:549–554. https://doi.org/10.1021/acsmedchemlett.7b00094

    Article  CAS  Google Scholar 

  10. Cristina-Silva C, Martins V, Gargaglioni LH, Bicego KC (2017) Mu and kappa opioid receptors of the periaqueductal gray stimulate and inhibit thermogenesis, respectively, during psychological stress in rats. Pflugers Arch - Eur J Physiol 469:1151–1161. https://doi.org/10.1007/s00424-017-1966-2

    Article  CAS  Google Scholar 

  11. El-Brolosy MA, Stainier DYR (2017) Genetic compensation: a phenomenon in search of mechanisms. PLoS Genet 13(7):e1006780. https://doi.org/10.1371/journal.pgen.1006780

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Everaerts W, Zhen X, Ghosh D, Vriens J, Gevaert T, Gilbert JP, Hayward NJ, McNamara CR, Xue F, Moran MM, Strassmaier T, Uykal E, Owsianik G, Vennekens R, De Ridder D, Nilius B, Fanger CM, Voets T (2010) Inhibition of the cation channel TRPV4 improves bladder function in mice and rats with cyclophosphamide-induced cystitis. Proc Natl Acad Sci U S A 107:19084–19089. https://doi.org/10.1073/pnas.1005333107

    Article  PubMed  PubMed Central  Google Scholar 

  13. Güler AD, Lee H, Iida T, Shimizu I, Tominaga M, Caterina M (2002) Heat-evoked activation of the ion channel, TRPV4. J Neurosci 22:6408–6414

    Article  PubMed  PubMed Central  Google Scholar 

  14. Karlsson U, Sundgren-Andersson AK, Johansson S, Krupp JJ (2005) Capsaicin augments synaptic transmission in the rat medial preoptic nucleus. Brain Res 1043:1–11. https://doi.org/10.1016/j.brainres.2004.10.064

    Article  CAS  PubMed  Google Scholar 

  15. Koteja P (1996) Measuring energy metabolism with open-flow respirometric systems: which design to choose? Funct Ecol 10:675–677

    Article  Google Scholar 

  16. Kumar H, Lee SH, Kim KT, Zeng X, Han I (2018) TRPV4: a sensor for homeostasis and pathological events in the CNS. Mol Neurobiol 55(11):8695–8708. https://doi.org/10.1007/s12035-018-0998-8

    Article  CAS  PubMed  Google Scholar 

  17. Kusudo T, Wang Z, Mizuno A, Suzuki M, Yamashita H (2012) TRPV4 deficiency increases skeletal muscle metabolic capacity and resistance against diet-induced obesity. J Appl Physiol 7:1223–1232. https://doi.org/10.1152/japplphysiol.01070.2011

    Article  CAS  Google Scholar 

  18. Lee H, Iida T, Mizuno A, Suzuki M, Caterina MJ (2005) Altered thermal selection behavior in mice lacking transient receptor potential vanilloid 4. J Neurosci 25:1304–1310. https://doi.org/10.1523/JNEUROSCI.4745.04.2005

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Li L, Yin J, Jie PH, Lu ZH, Zhou LB, Chen L, Chen L (2013a) Transient receptor potential vanilloid 4 mediates hypotonicity-induced enhancement of synaptic transmission in hippocampal slices. CNS Neurosci Ther 19:854–862. https://doi.org/10.1111/cns.1214

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Li L, Qu W, Zhou L, Lu Z, Jie P, Chen L, Chen L (2013b) Activation of transient receptor potential vanilloid 4 increases NMDA-activated current in hippocampal pyramidal neurons. Front Cell Neurosci 7:1–10. https://doi.org/10.3389/fncel.2013.00017

    Article  CAS  Google Scholar 

  21. Liedtke W, Choe Y, Marti-Renom MA, Bell AM, Denis CS, Sali A, Hudspeth AJ, Friedman JM, Heller S (2000) Vanilloid receptor-related osmotically activated channel (VR-OAC), a candidate vertebrate osmoreceptor. Cell 103:525–535. https://doi.org/10.1016/S0092-8674(00)00143-4

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  22. Lighton JRB (2008) Flow-through respirometry: the equations. In: Lighton JRB (ed) Measuring metabolic rates. A manual for scientists. Oxford University Press, New York, pp 100–104

    Chapter  Google Scholar 

  23. Morrison SF (2016) Central control of body temperature. F1000 Res. https://doi.org/10.12688/f1000research.7958.1

  24. Morrison SF, Nakamura K (2011) Central neural pathways for thermoregulation. Front Biosci 16:74–104

    Article  CAS  PubMed Central  Google Scholar 

  25. Nakamura K (2011) Central circuitries for body temperature regulation and fever. Am J Physiol Regul Integr Comp Physiol 301:R1207–R1228. https://doi.org/10.1152/ajpregu.00109.2011

    Article  CAS  PubMed  Google Scholar 

  26. Nakamura K, Morrison SF (2007) Central efferent pathways mediating skin cooling-evoked sympathetic thermogenesis in brown adipose tissue. Am J Physiol Regul Integr Comp Physiol 292:R127–R136. https://doi.org/10.1152/ajpregu.00427.2006

    Article  CAS  PubMed  Google Scholar 

  27. Nakamura K, Morrison SF (2008) Preoptic mechanism for cold-defensive responses to skin cooling. J Physiol 586:2611–2620. https://doi.org/10.1113/jphysiol.2008.152686

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  28. Nakamura K, Morrison SF (2010) A thermosensory pathway mediating heat-defense responses. Proc Natl Acad Sci U S A 107:8848–8853. https://doi.org/10.1073/pnas.0913358107

    Article  PubMed  PubMed Central  Google Scholar 

  29. Patapoutian A, Peier AM, Story GM, Viswanath V (2005) ThermoTRP channels and beyond: mechanisms of temperature sensation. Nat Rev Neurosci 4:529–539. https://doi.org/10.1038/nrn1141

    Article  CAS  Google Scholar 

  30. Paxinos G, Watson C (2005) The rat brain in stereotaxic coordinates. Elsevier Academic Press, San Diego

    Google Scholar 

  31. Romanovsky AA, Simons CT, Kulchitsky VA (1998) “Biphasic” fevers often consist of more than two phases. Am J Physiol Regul Integr Comp Physiol 275:R323–R331

    Article  CAS  Google Scholar 

  32. Romanovsky AA, Ivanov AI, Shimansky YP (2002) Molecular biology of thermoregulation: selected contribution: ambient temperature for experiments in rats: a new method for determining the zone of thermal neutrality. J Appl Physiol 92:2667–2679

    Article  PubMed  Google Scholar 

  33. Scarpellini CS, Gargaglioni LH, Branco LGS, Bícego KC (2009) Role of preoptic opioid receptors in the body temperature reduction during hypoxia. Brain Res 1286:66–74. https://doi.org/10.1016/j.brainres.2009.06.039

    Article  CAS  Google Scholar 

  34. Shibasaki K, Suzuki M, Mizuno A, Tominaga A (2007) Effects of body temperature on neural activity in the hippocampus: regulation of resting membrane potentials by transient receptor potential vanilloid 4. J Neurosci 27:1566–1575. https://doi.org/10.1523/JNEUROSCI.4284-06.2007

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Shibasaki K, Ikenaka K, Tamalu F, Tominaga M, Ishizaki Y (2014) A novel subtype of astrocytes expressing TRPV4 (transient receptor potential vanilloid 4) regulates neuronal excitability via release of gliotransmitters. J Biol Chem 289:14470–14480. https://doi.org/10.1074/jbc.M114.557132

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  36. Shibasaki K, Sugio S, Takao K, Yamanaka A, Miyakawa T, Tominaga M, Ishizaki Y (2015) TRPV4 activation at the physiological temperature is a critical determinant of neuronal excitability and behaviour. Pflugers Arch 467:2495–2507. https://doi.org/10.1007/s00424-015-1726-0

    Article  CAS  PubMed  Google Scholar 

  37. Steiner AA, Rocha MJA, Branco LGS (2002a) A neurochemical mechanism for hypoxia-induced anapyrexia. Am J Physiol Regul Integr Comp Physiol 283:1412–1422. https://doi.org/10.1152/ajpregu.00328.2002

    Article  Google Scholar 

  38. Steiner AA, Rodrigues JA, Branco LG (2002b) Role of preoptic second messenger systems (cAMP and cGMP) in the febrile response. Brain Res 944:135–145

    Article  CAS  PubMed  Google Scholar 

  39. Steiner AA, Rodrigues JA, McCann SM, Branco LG (2002c) Antipyretic role of the NO-cGMP pathway in the anteroventral preoptic region of the rat brain. Am J Physiol Regul Integr Comp Physiol 282:584–593. https://doi.org/10.1152/ajpregu.00391.2001

    Article  Google Scholar 

  40. Vizin RCL, Scarpellini CS, Ishikawa DT, Correa GM, Souza C, Gargaglioni LH, Carretiero DC, Bícego KC, Almeida MC (2015) TRPV4 activates autonomic and behavioural warmth defence responses in Wistar rats. Acta Physiol (Oxf) 214:275–289. https://doi.org/10.1111/apha.12477

    Article  CAS  Google Scholar 

  41. Watanabe H, Vriens J, Suh SH, Benham CD, Droogmans G, Nilius B (2002) Heat-evoked activation of TRPV4 channels in a HEK293 cell expression system and in native mouse aorta endothelial cells. J Biol Chem 277:47044–47051. https://doi.org/10.1074/jbc.M208277200

    Article  CAS  PubMed  Google Scholar 

  42. Wechselberger M, Wright CL, Bishop GA, Boulant JA (2006) Ionic channels and conductance-based models for hypothalamic neuronal thermosensitivity. Am J Physiol Regul Integr Comp Physiol 291:R518–R529. https://doi.org/10.1152/ajpregu.00039.2006

    Article  CAS  PubMed  Google Scholar 

  43. Zhou YD (2018) Glial regulation of energy metabolism. In: Wu Q., Zheng R. (eds) Neural regulation of metabolism. Advances in experimental medicine and biology. Springer, Singapore, pp 105–121

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Acknowledgments

This study was part of the activities developed by C.S.S. for obtaining a Ph.D degree at the Joint Graduate Program in Physiological Sciences (PIPGCF) from UFSCar/UNESP. We thank Euclides Roberto Secato for his technical assistance.

Funding

This work was financially supported by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP: Grant 15/04849-6 to K.C.B.; Grant 15/02991-0 to M.C.A; Ph.D. fellowship 2011/19131-2 to C.S.S.; Ph.D. fellowship 2017/17278-2 to C.C-S; Ph.D. fellowship 2012/15298-2 to V.B.) and Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq: Grant 442560/2014-1 to L.H.G).

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Contributions

C.S.S., K.C.B. and M.C.A.—conception and design

K.C.B., M.C.A. and L.H.G.—financial support

C.S.S., C.C-S. and V.B.—collection and assembly of data

C.S.S., C.C-S, V.B., K.C.B. and M.C.A.—data analysis and interpretation

C.S.S., C.C-S, V.B., K.C.B., L.H.G. and M.C.A.—manuscript writing

Corresponding authors

Correspondence to Carolina da Silveira Scarpellini or Kênia Cardoso Bícego.

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All procedures were approved by the local Animal Care and Use Committee of São Paulo State University (CEUA/FCAV, Protocol Number 019288/14).

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Scarpellini, C.d., Cristina-Silva, C., Biancardi, V. et al. Hypothalamic TRPV4 channels participate in the medial preoptic activation of warmth-defence responses in Wistar male rats. Pflugers Arch - Eur J Physiol 471, 1191–1203 (2019). https://doi.org/10.1007/s00424-019-02303-1

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