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dc.contributor.authorNameni, G
dc.contributor.authorHajiluian, G
dc.contributor.authorShahabi, P
dc.contributor.authorFarhangi, MA
dc.contributor.authorMesgari-Abbasi, M
dc.contributor.authorHemmati, MR
dc.contributor.authorVatandoust, SM
dc.date.accessioned2018-08-26T07:20:39Z
dc.date.available2018-08-26T07:20:39Z
dc.date.issued2017
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/45954
dc.description.abstractThere is growing evidence that obesity can lead to neurodegeneration induced by pro-inflammatory cytokines such as tumor necrosis factor (TNF-alpha). Moreover, obesity is associated with reduced transport of insulin through the blood-brain barrier (BBB). Insulin deficiency in the brain especially in the hypothalamus region has neurodegenerative and obesity-promoting effects. Because of the anti-inflammatory and neuroprotective effects of vitamin D, in the current experimental study, we aimed to investigate the effects of vitamin D supplementation on neurodegeneration, TNF-a concentration in the hypothalamus, and cerebrospinal fluid (CSF) to serum ratio of insulin in high-fat-diet-induced obese rats. At the first phase of the study, the rats were divided into two groups: (1) normal diet (ND, 10% fat) and (2) high-fat diet (HFD, 59% fat) and were fed for 16 weeks. In the second phase, each group was subdivided into four groups including the following: ND, normal diet + vitamin D, HFD, and HFD + vitamin D. Weight was measured and recorded weekly. Vitamin D supplementation for 5 weeks at 500 IU/kg dosage was used. One week after vitamin D supplementation, daily food intake was recorded. At week 22, blood was collected to determine fasting serum glucose, vitamin D, and insulin concentrations, and the homeostasis model assessment of insulin resistance (HOMA-IR) was calculated. CSF samples were also collected to measure insulin concentrations, and the hypothalamus was dissected to determine TNF-a concentration. HFD significantly increased TNF-a concentrations and degenerated neurons in the hypothalamus (P = 0.02). We also observed a significant reduction of CSF-to-serum ratio of insulin in HFD group (P = 0.03). The HOMA-IR test indicated significant increment of insulin resistance in HFD-fed rats (P = 0.006). Vitamin D supplementation in HFD group significantly reduced weight (P = 0.001) and food intake (P = 0.008) and increased CSF-to-serum ratio of insulin (P = 0.01). Furthermore, vitaminD decreased insulin resistance in the HFD group (P = 0.008). Vitamin D had no significant effect on degenerated neurons and TNF-a concentration in the hypothalamus. According to our findings, vitamin D improved brain insulin homeostasis and modulated food intake and body weight in high-fat-dietinduced obese rats. Further studies are needed to better clarify the underlying mechanisms.
dc.language.isoEnglish
dc.relation.ispartofJOURNAL OF MOLECULAR NEUROSCIENCE
dc.subjectNeurodegeneration
dc.subjectTNF-alpha
dc.subjectInsulin
dc.subjectVitamin D
dc.subjectObesity
dc.titleThe Impact of Vitamin D Supplementation on Neurodegeneration, TNF-alpha Concentration in Hypothalamus, and CSF-to-Plasma Ratio of Insulin in High-Fat-Diet-Induced Obese Rats
dc.typeArticle
dc.citation.volume61
dc.citation.issue2
dc.citation.spage247
dc.citation.epage255
dc.citation.indexWeb of science
dc.identifier.DOIhttps://doi.org/10.1007/s12031-016-0864-y


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