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Age-specific mortality and fecundity of a spider mite under diet restriction and delayed mating

Insect Science 2022年第3期29卷 889-899页

作者： Guang-Yun Li Zhi-Qiang Zhang Centre for Biodiversity and Biosecurity School of Biological SciencesUniversity of AucklandAucklandNew Zealand Manaaki Whenua-Landcare Research AucklandNew Zealand Key Laboratory of Entomology and Pest Control Engineering College of Plant ProtectionSouthwest UniversityChongqingChina

Numerous experimental life-history studies on aging are mainly baised on two classical models—fruit fly Drosophila melanogaster(Meigen)and nematode Caenorhab-ditis elegans(Maupas)—with relatively little attention given to other organisms with different life-history characters.Two-spotted spider mite Tetranychus urticae Koch(Acari:Tetranychidae)differs from many other arthropods in that the females continue their growth in the early adult stage and can reproduce sexually and asexually.In this study,the influences of dietary restriction and delayed mating on the aging patterns of the spider mite were examined with the prevailing survival and reproduction trade-off hypothesis of aging being tested.Significant sex-specific responses of the spider mites were found.The females showed longevity extension on diet restriction(fasting for 2 days in every 4 days)compared with their counterparts being fed ad libitum,and after delayed mating for 9 days,while the males displayed a decrease in lifespan when experiencing diet restriction but were not significantly influenced by delayed mating.Path analysis was used to investigate the relationship between mite survival and reproduction traits,including longevity,female lifetime reproduction,age at first reproduction,early reproductive efforts and late reproductive efforts,yielding no evidence for trade-offs between these life-history traits.The additive effects of dietary restriction and delayed mating in lifespan extension of female spider mites were confirmed,proving that diet restriction is a robust anti-aging intervention,and that later onset of reproduction can prolong adult lifespan in females.

关键词： age-specific mortality delayed mating diet restriction reproduction sex difference trade-off

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Low Expression of FGF23 and Its Effect on Rats with Intrauterine Growth Retardation

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Maternal-Fetal Medicine 2020年第4期2卷 211-216页

作者： Gui Shun-Ping Zou Heng Bai Yi Liu Min Wang Tao Zhou Rong Department of Obstetrics and Gynecology West China Second University HospitalSichuan UniversityChengduSichuan 610041China Key Laboratory of Birth Defects and Related Diseases of Women and Children(Sichuan University)of Ministry of Education ChengduSichuan 610041China Laboratory of Molecular and Translational Medicine West China Second University HospitalSichuan UniversityChengduSichuan 610041China

Objective:To explore the levels of fibroblast growth factor 23(FGF23)during pregnancy and its relationship with intrauterine growth restriction(IUGR).Methods:Pregnant rats were classified into an ad libitum rat chow group(ad libitum rat chow,AD group,n=25)and an undernutrition group(50%of their daily food requirement,UN group,n=25).The levels of maternal serum FGF23,tissue homogenate FGF23,and bone gla protein in fetal rats,and placental FGF23 mRNA and protein expression were examined by enzyme-linked immunosorbent assay,real-time qPCR analysis respectively.Finally,the effect of recombinant FGF23 on the viability of MG-63 cells was determined by cell proliferation assay.Data were analyzed with independent two-tailed t test and one-way analysis of variance.Spearman rank-order correlation coefficients(continuous variables)was performed to determine the relationship of results.Results:The diet restriction induced IUGR in rat offsprings,and the UN group exhibited a significantly lower FGF23 level(P<0.05,n=5).The FGF23 level was increased and peaked in maternal serum on gestation day(GD)15,but peaked in fetal and placenta on GD20.Moreover,the tissue homogenate levels of FGF23 and bone gla protein in fetal rats in both groups were positively correlated(r=0.923,P<0.05;r=0.925,P<0.05,respectively,n=15),FGF23 was localized to both decidual and labyrinth zones,with remarkably higher expression on GD20,P<0.05,n=5.In vitro,recombinant human FGF23 enhanced MG-63 cell viability,P<0.05,n=5.Conclusion:Prenatal undernutrition could decrease the FGF23 expression in fetal rats caused by the mother through the placenta,and induced the IUGR and hindered the ossification.And the FGF23 levels are peaked on GD15 mother but peaked on GD20 placenta and fetuses,these might be associated with the over compensation of maternal placenta on GD20.

关键词： Fetal growth retardation FGF23 BGP diet restriction Rats

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