PACAP is essential for the adaptive thermogenic response of brown adipose tissue to cold exposure

Abdoulaye Diane, Nikolina Nikolic, Alexander P. Rudecki, Shannon M. King, Drew J. Bowie, Sarah L. Gray

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Pituitary adenylate cyclase-activating polypeptide (PACAP) is a widely distributed neuropeptide that acts as a neurotransmitter, neuromodulator, neurotropic factor, neuroprotectant, secretagogue, and neurohormone. Owing to its pleiotropic biological actions, knockout of Pacap (Adcyap1) has been shown to induce several abnormalities in mice such as impaired thermoregulation. However, the underlying physiological and molecular mechanisms remain unclear. A previous report has shown that cold-exposed Pacap null mice cannot supply appropriate levels of norepinephrine (NE) to brown adipocytes. Therefore, we hypothesized that exogenous NE would rescue the impaired thermogenic response of Pacap null mice during cold exposure. We compared the adaptive thermogenic capacity of Pacap-/- to Pacap+/+ mice in response to NE when housed at room temperature (24 °C) and after a 3.5-week cold exposure (4 °C). Biochemical parameters, expression of thermogenic genes, and morphological properties of brown adipose tissue (BAT) and white adipose tissue (WAT) were also characterized. Results showed that there was a significant effect of temperature, but no effect of genotype, on the resting metabolic rate in conscious, unrestrained mice. However, the normal cold-induced increase in the basal metabolic rate and NE-induced increase in thermogenesis were severely blunted in cold-exposed Pacap-/- mice. These changes were associated with altered substrate utilization, reduced β3-adrenergic receptor (β3-Ar (Adrb3)) and hormone-sensitive lipase (Hsl (Lipe)) gene expression, and increased fibroblast growth factor 2 (Fgf2) gene expression in BAT. Interestingly, Pacap-/-mice had depletedWAT depots, associated with upregulated uncoupling protein 1 expression in inguinal WATs. These results suggest that the impairment of adaptive thermogenesis in Pacap null mice cannot be rescued by exogenous NE perhaps in part due to decreased β3-Ar-mediated BAT activation.

Original languageEnglish
Pages (from-to)327-339
Number of pages13
JournalJournal of Endocrinology
Volume222
Issue number3
DOIs
Publication statusPublished - 1 Jan 2014
Externally publishedYes

Fingerprint

Pituitary Adenylate Cyclase-Activating Polypeptide
Brown Adipose Tissue
Norepinephrine
Neurotransmitter Agents
Basal Metabolism
Thermogenesis
Gene Expression
Brown Adipocytes
Sterol Esterase
White Adipose Tissue
Temperature
Groin
Body Temperature Regulation
Neuroprotective Agents
Fibroblast Growth Factor 2
Neuropeptides
Adrenergic Receptors
Genotype

Keywords

  • Cold
  • Gene expression
  • Mice
  • PACAP
  • Thermogenesis

ASJC Scopus subject areas

  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

Cite this

Diane, A., Nikolic, N., Rudecki, A. P., King, S. M., Bowie, D. J., & Gray, S. L. (2014). PACAP is essential for the adaptive thermogenic response of brown adipose tissue to cold exposure. Journal of Endocrinology, 222(3), 327-339. https://doi.org/10.1530/JOE-14-0316

PACAP is essential for the adaptive thermogenic response of brown adipose tissue to cold exposure. / Diane, Abdoulaye; Nikolic, Nikolina; Rudecki, Alexander P.; King, Shannon M.; Bowie, Drew J.; Gray, Sarah L.

In: Journal of Endocrinology, Vol. 222, No. 3, 01.01.2014, p. 327-339.

Research output: Contribution to journalArticle

Diane, A, Nikolic, N, Rudecki, AP, King, SM, Bowie, DJ & Gray, SL 2014, 'PACAP is essential for the adaptive thermogenic response of brown adipose tissue to cold exposure', Journal of Endocrinology, vol. 222, no. 3, pp. 327-339. https://doi.org/10.1530/JOE-14-0316
Diane, Abdoulaye ; Nikolic, Nikolina ; Rudecki, Alexander P. ; King, Shannon M. ; Bowie, Drew J. ; Gray, Sarah L. / PACAP is essential for the adaptive thermogenic response of brown adipose tissue to cold exposure. In: Journal of Endocrinology. 2014 ; Vol. 222, No. 3. pp. 327-339.
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