Journal
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
Volume 315, Issue 1, Pages R134-R143Publisher
AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpregu.00049.2018
Keywords
dihydrocapsaicin; raphe pallidus; resiniferatoxin; sympathetic nerve activity; thermoregulation
Categories
Funding
- National Institutes of Health [R01-NS-091066, R01-DK-112198, R01-HL-133505]
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The sympathetic nerve activity (SNA) to brown adipose tissue (BAT) regulates BAT thermogenesis to defend body temperature in cold environments or to produce fever during immune responses. The vagus nerve contains afferents that inhibit the BAT SNA and BAT thermogenesis evoked by skin cooling. We sought to determine whether activation of transient receptor potential vanilloid 1 (TRPV1) channels in the nucleus tractus solitarius (NTS), which are prominently expressed in unmyelinated vagal afferents, would affect coldevoked BAT thermogenesis, cardiovascular parameters, or their vagal afferent-evoked responses. In urethane-chloralose-anesthetized rats, during skin cooling, nanoinjection of the TRPV 1 -agonist resiniferatoxin in NTS decreased BAT SNA (from 695 +/- 195% of baseline during cooling to 103 +/- 8% of baseline after resiniferatoxin), BAT temperature (-0.8 +/- 0.1 degrees C), expired CO2 (-0.3 +/- 0.04%), mean arterial pressure (MAP; -20 +/- 5 mmHg), and heart rate (-44 +/- 11 beats/min). Pretreatment of NTS with the TRPV1 antagonist capsazepine prevented these resiniferatoxin-medialed effects. Intravenous injection of the TRPV 1 agonist dihydrocapsaicin also decreased all the measured variables (except MAP). Bilateral cervical or subdiaphragmatic vagotomy attenuated the decreases in BAT SNA and thermogenesis evoked by nanoinjection of resiniferatoxin in NTS but did not prevent the decreases in BAT SNA and BAT thermogenesis evoked by intravenous dihydrocapsaicin. We conclude that activation of TRPVJ channels in the NTS of vagus nerve intact rats inhibits BAT SNA and decreases BAT metabolism, blood pressure, and heart rate. In contrast, the inhibition of BAT thermogenesis following systemic administration of dihydrocapsaicin does not require vagal afferent activity, consistent with a nonvagal pathway through which systemic TRPV1 agonists can inhibit BAT thermogenesis.
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