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INTRODUCTION: Obesity is a global issue and a major metabolic disorder, leading to the development of serious diseases such as diabetes type 2 (DM2). Importantly, DM2 accounts for over 90 % of the diabetic cases in human. There are also sex‑specific differences in the development of obesity and DM2. The arcuate nucleus of the hypothalamus (ARC) is believed to be central to integration of peripheral and central anabolic and catabolic inputs and the maintenance of energy balance. Neuropeptide Y (NPY) neurons plays a role in the regulation of food intake and modulation of energy expenditure. In rat brain, NPY neurons are located in the ARC and send projections to numerous other hypothalamic regions. However, there is no data concerning the comparison of the role of diet-induced obesity and DM2 on these neurons in male and female rats. AIM(S): The aim of this project was to study the effects of obesity and DM2 on NPY-immunoreactivity in the ARC of the hypothalamus of male and female rats. METHOD(S): To induce obesity female and male Wistar rats were fed with a high fat diet (HFD). In order to mimic the DM2 condition, a subset of HFD animals were injected with streptozotocin (a toxin that destroys pancreatic cells). The control group received lab chow diet. Animals were sacrificed, perfused with paraformaldehyde, and blood and brains were collected for further analysis. Blood was used to assess the metabolic and hormonal status of the animals and brains were processed for immunohistochemistry. RESULTS: Analysis of metabolic and hormonal status confirmed induction of obesity and DM2 in animals. Preliminary data (n=3) indicate an increase in NPY‑immunostaining in the ARC of obese male and female rats compared to controls. Currently the remaining data are being analyzed. CONCLUSIONS: The preliminary data indicate that HFD-induced obesity may alter functions of NPY neurons in the ARC of male and female rats. FINANCIAL SUPPORT: Supported by OPUS NCN grant2015/17/B/NZ4/02021.
INTRODUCTION: There is a strong evidence that neurons co-expressing kisspeptin (KP), neurokinin B (NKB) and dynorphin (Dyn), so called KNDy neurons, are important factors governing the hypothalamic-pituitary-gonadal axis. These neurons are present in the arcuate nucleus of the hypothalamus (ARC), which is also a region involved in energy homeostasis. It was shown that expression of KP, NKB and Dyn is dependent on hormonal and metabolic status. We have previous found that type 2 diabetes but not diet-induced obesity increases number of KP-, NKB- and non-pregnant ewes and ewes euthanized at 30, 60, 90, 120 d of pregnancy (3 ewes/group). Real-time PCR was used to measure SOCS-3 mRNA abundance. RESULTS: Results showed that SOCS-3 transcript level increased in MBH at 30, 60 and 90 d of gestation in comparison with non-pregnant ewes (P<0.05). The greatest SOCS-3 transcript abundance was observed at 120 d of pregnancy in ARC and in AP. In ME, SOCS‑3 expression significantly decreased (P<0.05) during early- and mid-pregnancy (at 30 and 60 d of gestation) but during late-pregnancy (120 d of gestation) it increased to a level comparable to that of non-pregnant ewes. In the CP, SOCS-3 mRNA expression in first half of pregnancy was similar to that observed in non-pregnant females, but increased markedly in the second half of pregnancy (P<0.05). Interestingly, SOCS-3 expression decreased throughout pregnancy in the PG (P<0.05). CONCLUSIONS: The pattern of expression of SOCS-3 differs among brain locations and by stage of pregnancy within brain and AP locations and variation in SOCS-3 transcripts may be one of the factors in brain and AP that mediate homeorhetic adjustments in metabolism during gestation. FINANCIAL SUPPORT: Research supported by grant from Polish National Science Centre no 2013/09/B/NZ4/01532.
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