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Reproductive BiologyVolume 17, Issue 1, 1 March 2017, Pages 19-24

Metabolic state defines the response of rabbit ovarian cells to leptin(Article)

  • aZoology Department, College of Science, King Saud University, Riyadh, Saudi Arabia
  • bCenter for Genomic Medicine, Copenhagen University Hospital, Copenhagen, Denmark
  • cDepartment of Zoology and Anthropology, Constantine the Philosopher University, Nitra, Slovakia
  • dDepartment of Genetics and Reproduction, Research Institute of Animal Production, Lužianky, Slovakia
  • eDepartment of Biotechnology, University of SS. Cyril and Methodius, Trnava, Slovakia

Abstract

Leptin is a hormone that mediates the effect of the metabolic state on several biological functions, including reproduction. Leptin affects reproductive functions via alterations in the release of hormonal regulators. However, the extent to which caloric restriction (CR) can affect the complex processes of reproduction by other mechanisms, such as altering ovarian functions via direct binding/response to leptin, is unknown. Therefore, the aim of the present study was to show basic ovarian cell functions and CR on the response of ovarian cells to leptin. Female rabbits were subjected to 50% CR restriction for 10 days before ovulation. On the day of ovulation, both control and CR animals were sacrificed. Isolated granulosa cells were cultured for 2 days with and without leptin (100 ng/ml), and the accumulation of various markers was evaluated using immunocytochemistry; i.e., cell proliferation (PCNA and cyclin B1), apoptosis (bax), MAP/ERK1,2 kinase (MAPK), protein kinase A (PKA), and IGF-I. In addition, the release of IGF-I and estradiol (E2) by cells cultured with and without leptin (1, 10, 100, 1000, or 10,000 ng/ml) was assessed by radioimmunoassay (RIA). In the granulosa cells of control animals, leptin promoted cyclin B1, MAPK, and PKA accumulation, but not that of PCNA, and reduced bax and IGF-I accumulation. These cells responded to leptin by increased IGF-I, but not E2 release. In cells of CR animals, leptin increased cyclin B1 accumulation, but decreased PCNA, MAPK, and IGF-I expression. Bax and PKA were not affected. Leptin resulted in a decrease in IGF-I release. CR modulated the influence of leptin on E2 release dose dependently, i.e., E2 increased at 10 and decreased at 10,000 ng/ml. Therefore, CR modified the influence of leptin on PCNA, E2, bax, PKA, MAPK, and IGF-I release, but it did not change the effect of leptin on cyclin B1 and IGF-I accumulation within the cells. Our data showed that leptin directly affected proliferation, apoptosis, and hormone release by ovarian cells, probably via PKA- and MAPK-dependent pathways. Furthermore, it was demonstrated that nutrition could influence reproduction by affecting the response of ovarian cells to leptin. © 2016 Society for Biology of Reproduction & the Institute of Animal Reproduction and Food Research of Polish Academy of Sciences in Olsztyn

Author keywords

  • Apoptosis
  • Caloric restriction
  • Hormones
  • Leptin
  • Ovary
  • Proliferation
  • Rabbit

Indexed keywords

EMTREE drug terms:biological markercyclic AMP dependent protein kinaseestradiolleptinrecombinant proteinsomatomedin C
EMTREE medical terms:adverse effectsanimalapoptosiscaloric restrictioncell culturecell proliferationcytologyfemalegeneticsgranulosa cellhumankineticsmetabolismovaryovulation inductionrabbits and haresrandomizationsecretion (process)signal transduction
MeSH:AnimalsApoptosisBiomarkersCaloric RestrictionCell ProliferationCells, CulturedCyclic AMP-Dependent Protein KinasesEstradiolFemaleGranulosa CellsHumansInsulin-Like Growth Factor IKineticsLeptinMAP Kinase Signaling SystemOvaryOvulation InductionRabbitsRandom AllocationRecombinant Proteins

Chemicals and CAS Registry Numbers:

cyclic AMP dependent protein kinase; estradiol, 50-28-2; somatomedin C, 67763-96-6;

Biomarkers; Cyclic AMP-Dependent Protein Kinases; Estradiol; Insulin-Like Growth Factor I; Leptin; Recombinant Proteins

Funding details

Funding numberFunding sponsorAcronym
0013King Saud UniversityKSU
VEGA 1/0327/16Agentúra na Podporu Výskumu a VývojaAPVV
RUVVR 07-13Ministry of Agriculture of the People's Republic of ChinaMOA

Funding text

The authors thank Ing. ? Kuklov?, Mrs K Tothov? and Ing. Ondru?ka for technical assistance and Mrs. G. Neuhaus for kind help in cell photography. This work was supported by Slovak Research and Development Agency under the contract No. APVV-14-0001 and was co-funded by the projects VEGA 1/0022/15, VEGA 1/0327/16, KEGA 001UKF-4/2016, and the Ministry of Agriculture of the Slovak Republic, project RUVVR 07-13. The authors would also like to extend their appreciation to the International Scientific Partnership Program ISPP at King Saud University for funding this research work through ISPP# 0013.

  • ISSN: 1642431X
  • Source Type: Journal
  • Original language: English
  • DOI: 10.1016/j.repbio.2016.11.002
  • PubMed ID: 27894742
  • Document Type: Article
  • Publisher: Elsevier B.V.

  Sirotkin, A.V.; Department of Zoology and Anthropology, Constantine the Philosopher University, Nitra, Slovakia;
© Copyright 2017 Elsevier B.V., All rights reserved.

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