Temperature- and capsaicin-sensitive nerve fibers in brown adipose tissue attenuate thermogenesis in the rat

• Published in: Pflügers Archiv Vol. 437; no. 1; pp. 36 - 42
• Main Authors: Osaka, T, Kobayashi, A, Namba, Y, Ezaki, O, Inoue, S, Kimura, S, Lee, T H
• Format: Journal Article
• Language: English
• Published: Germany Springer Nature B.V 01.12.1998
• Subjects: Adipocytes; Adipose Tissue, Brown - innervation; Animals; Body Temperature Regulation - physiology; Calcitonin Gene-Related Peptide - pharmacology; Capsaicin - pharmacology; Denervation; Female; Hot Temperature; Nerve Fibers - drug effects; Nerve Fibers - physiology; Norepinephrine - pharmacology; Rats; Rats, Sprague-Dawley; Rodents; Substance P - pharmacology; Temperature
• ISSN: 0031-6768; 1432-2013
• DOI: 10.1007/s004240050743

We examined the function of putative sensory fibers that are contained in intercostal nerves and innervate interscapular brown adipose tissue (IBAT) in urethane-anesthetized rats. Warming the IBAT to 40-44 degrees C with two small heaters placed bilaterally on the skin above it attenuated the subsequent noradrenaline-induced thermogenesis (NIT) of the IBAT. In this range of warming, higher IBAT temperatures resulted in more attenuation. Denervation of IBAT blocked the effect of thermal stimulation on the NIT. Thus, activation of nerve fibers in IBAT that are sensitive to warmth or to the nociceptive effects of heat probably attenuated the NIT. Since the putative sensory fibers in the IBAT contain calcitonin gene-related peptide (CGRP) and substance P, which are thought to act in peripheral tissues, we tested the effects of injection of these neuropeptides into the IBAT. Administration of 5.2 nmol CGRP but not substance P or vehicle saline mimicked the effect of thermal stimulation of IBAT. As the neuropeptide-containing primary sensory neurons are characterized by their sensitivity to capsaicin, we also tested its effects (1 mg/kg, s.c.) and found that it also attenuated the NIT. Denervation of the IBAT or pretreatment with capsazepine, a capsaicin receptor antagonist, blocked the effect of capsaicin. We propose that temperature- and capsaicin-sensitive nerve fibers release CGRP to attenuate the NIT of brown adipocytes.