期刊
JOURNAL OF NEUROENDOCRINOLOGY
卷 25, 期 6, 页码 580-589出版社
WILEY
DOI: 10.1111/jne.12033
关键词
obesity; NPY; IL-6 receptor; IL-6 knockout; IL-1R1 knockout
资金
- Swedish Research Council [K2007/54X/09894/16/3, 521-2003-5116, 521-2003-4312, k2007-54x-20328-013]
- Novo Nordisk Foundation (GeA/AIR)
- Stiftelsen Thornspiran
- Royal Society of Arts and Sciences in Goteborg
- Swedish Medical Society
- Swedish Society for Medical Research
- Lars Hierta Memorial Foundation
- ALF Goteborg [SU7601]
- Swedish Foundation for Strategic Research [A305-188]
- European Union [266408]
Interleukin (IL)-1 and IL-6 are immune modulating cytokines that also affect metabolic function because both IL-1 receptor I deficient (IL-1RI-/-) and IL-6 deficient (IL-6-/-) mice develop late-onset obesity and leptin resistance. Both IL-1 and IL-6 appear to target the central nervous system (CNS) to increase energy expenditure. The hypothalamic arcuate nucleus (ARC) is a major relay between the periphery and CNS in body fat regulation (e.g. by being a target of leptin). The present study aimed to investigate the possible mechanisms responsible for the effects exerted by endogenous IL-1 and IL-6 on body fat at the level of the ARC, as well as possible interactions between IL-1 and IL-6. Therefore, we measured the gene expression of neuropeptides of the ARC involved in energy balance in IL-1RI-/- and IL-6-/- mice. We also investigated the interactions between expression of IL-1 and IL-6 in these mice, and mapped IL-6 receptor (IL-6R) in the ARC. The expression of the obesity promoting peptide neuropeptide Y (NPY), found in the ARC, was increased in IL-1RI-/- mice. The expression of NPY and agouti-related peptide (AgRP), known to be co-expressed with NPY in ARC neurones, was increased in cold exposed IL-6-/- mice. IL-6R immunoreactivity was densely localised in the ARC, especially in the medial part, and was partly found in NPY positive cell bodies and also -melanocyte-stimulating hormone positive cell bodies. The expression of hypothalamic IL-6 was decreased in IL-1RI-/- mice, whereas IL-1 ss expression was increased in IL-6-/- mice. The results of the present study indicate that depletion of the activity of the fat suppressing cytokines IL-1 and IL-6 in knockout mice can increase the expression of the obesity promoting neuropeptide NPY in the ARC. Depletion of IL-1 activity suppresses IL-6 expression, and IL-6R-like immunoreactivity is present in neurones in the medial ARC, including neurones containing NPY. Therefore, IL-6, IL-1 and NPY/AgRP could interact at the level of the hypothalamic ARC in the regulation of body fat.
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