Literature DB >> 16352410

Recent female mouse models displaying advanced reproductive aging.

Natalia Danilovich1, M Ram Sairam.   

Abstract

Reproductive senescence occurs in all female mammals with resultant changes in numerous body functional systems and several important features may be species-specific. Those features that appear to parallel human menopause and aging include general similarity of hormone profiles across the menopausal transition, progression to cycle termination through irregular cycles, declining fertility with age, disturbances in thermogenesis, age-related gains in body weight, fat distribution and disposition towards metabolic syndrome. Structural and hormonal changes in the brain and ovary play a critical role in determining the onset of reproductive senescence. The short life span of rodents such as mice (compared to humans) and the ability to generate specific and timed gene deletions, provide powerful experimental paradigms to understand the molecular and functional changes that precede and follow the loss of reproductive capacity. In theory, any manipulation that compromises ovarian function either partly or totally would impact reproductive events at various levels followed by other dysfunctions. In this article, we provide an overview of three mouse models for the study of female reproductive aging. They are derived from different strategies and their age related phenotypes have been characterized to varying degrees. The follitropin receptor knockout (FORKO) mouse, in its null and haploinsufficient state as well as the dioxin/aryl hydrocarbon receptor (AhR) knockout mouse, serve as two examples of single gene deletions. A third model, using administration of a chemical toxicant such as 4-vinylcyclohexene diepoxide (VCD) in the adult state, produces ovarian deficiencies accompanied by aging changes. These will serve as useful alternatives to previously used radical ovariectomy in young adults. It is anticipated that these new models and more that will be forthcoming will extend opportunities to understand reproductive aging and resolve controversies that abound on issues related to benefits and risks of hormone replacement therapy or other modalities for improving quality of life.

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Year:  2005        PMID: 16352410     DOI: 10.1016/j.exger.2005.10.010

Source DB:  PubMed          Journal:  Exp Gerontol        ISSN: 0531-5565            Impact factor:   4.032


  15 in total

1.  Modeling perimenopause in Sprague-Dawley rats by chemical manipulation of the transition to ovarian failure.

Authors:  Jennifer B Frye; Ashley L Lukefahr; Laura E Wright; Sam L Marion; Patricia B Hoyer; Janet L Funk
Journal:  Comp Med       Date:  2012-06       Impact factor: 0.982

Review 2.  Early reproductive experiences in females make differences in cognitive function later in life.

Authors:  Rena Li; Jie Cui; Balaji Jothishankar; Juliet Shen; Ping He; Yong Shen
Journal:  J Alzheimers Dis       Date:  2013       Impact factor: 4.472

3.  Estradiol treatment, physical activity, and muscle function in ovarian-senescent mice.

Authors:  Sarah M Greising; Ryan S Carey; Jennifer E Blackford; Laurin E Dalton; Allison M Kosir; Dawn A Lowe
Journal:  Exp Gerontol       Date:  2011-05-04       Impact factor: 4.032

4.  Prediction of ovarian aging using ovarian expression of BMP15, GDF9, and C-KIT.

Authors:  Min Jung Park; Jun-Woo Ahn; Ki Hyung Kim; Junghee Bang; Seung Chul Kim; Jae Yi Jeong; Ye Eun Choi; Chang-Woon Kim; Bo Sun Joo
Journal:  Exp Biol Med (Maywood)       Date:  2020-03-29

5.  Accelerated ovarian aging in mice by treatment of busulfan and cyclophosphamide.

Authors:  Yan Jiang; Jing Zhao; Hui-jing Qi; Xiao-lin Li; Shi-rong Zhang; Daniel W Song; Chi-yang Yu; Jian-gang Gao
Journal:  J Zhejiang Univ Sci B       Date:  2013-04       Impact factor: 3.066

6.  Epab and Pabpc1 are differentially expressed in the postnatal mouse ovaries.

Authors:  Saffet Ozturk; Berna Sozen; Necdet Demir
Journal:  J Assist Reprod Genet       Date:  2014-11-05       Impact factor: 3.412

Review 7.  Accelerated ovarian failure: a novel, chemically induced animal model of menopause.

Authors:  Tracey A Van Kempen; Teresa A Milner; Elizabeth M Waters
Journal:  Brain Res       Date:  2011-01-04       Impact factor: 3.252

8.  White spotting variant mouse as an experimental model for ovarian aging and menopausal biology.

Authors:  Elizabeth R Smith; Toni Yeasky; Jain Qin Wei; Roberto A Miki; Kathy Q Cai; Jennifer L Smedberg; Wan-Lin Yang; Xiang-Xi Xu
Journal:  Menopause       Date:  2012-05       Impact factor: 2.953

9.  The presence of the ovary prevents hepatic mitochondrial oxidative stress in young and aged female mice through glutathione peroxidase 1.

Authors:  Ana P Valencia; Anna E Schappal; E Matthew Morris; John P Thyfault; Dawn A Lowe; Espen E Spangenburg
Journal:  Exp Gerontol       Date:  2015-12-01       Impact factor: 4.032

10.  Daily exercise prevents diastolic dysfunction and oxidative stress in a female mouse model of western diet induced obesity by maintaining cardiac heme oxygenase-1 levels.

Authors:  Brian Bostick; Annayya R Aroor; Javad Habibi; William Durante; Lixin Ma; Vincent G DeMarco; Mona Garro; Melvin R Hayden; Frank W Booth; James R Sowers
Journal:  Metabolism       Date:  2016-09-22       Impact factor: 8.694

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