Literature DB >> 9048626

Leptin treatment rescues the sterility of genetically obese ob/ob males.

K Mounzih1, R Lu, F F Chehab.   

Abstract

Leptin, a hormone secreted from white adipose tissue, has been shown to normalize the body weight of ob/ob but not db/db mice as postulated by Coleman in his classical parabiosis experiments. The major effect of leptin is therefore to decrease food intake, thus resulting in a breakdown of fat stores. Recently, we have suggested that leptin plays a role in reproductive physiology based on the observation that leptin treatment but not food restriction rescues the sterility of ob/ob females. In the present communication, we treated sterile ob/ob males with leptin and asked whether fertility could be induced, thus selecting their reproductive ability as the endpoint of the experiment. Our results show that all food-restricted ob/ob males are unable to impregnate normal C57BL/6J females. However, all leptin-treated ob/ob males fertilized normal females mice that carried out normal pregnancies and deliveries, demonstrating that the reproductive capacity of ob/ob males was corrected only with leptin treatment. Furthermore, reproductive indices such as testicular weight and histology are normalized in leptin-treated animals. Therefore, as in ob/ob females, leptin plays a significant role in the male mouse reproductive pathways.

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Year:  1997        PMID: 9048626     DOI: 10.1210/endo.138.3.5024

Source DB:  PubMed          Journal:  Endocrinology        ISSN: 0013-7227            Impact factor:   4.736


  87 in total

1.  Leptin and puberty.

Authors:  P E Clayton; J A Trueman
Journal:  Arch Dis Child       Date:  2000-07       Impact factor: 3.791

Review 2.  Metabolic regulation is important for spermatogenesis.

Authors:  Luís Rato; Marco G Alves; Sílvia Socorro; Ana I Duarte; José E Cavaco; Pedro F Oliveira
Journal:  Nat Rev Urol       Date:  2012-05-01       Impact factor: 14.432

3.  Mammary ductal growth is impaired in mice lacking leptin-dependent signal transducer and activator of transcription 3 signaling.

Authors:  Stephanie R Thorn; Sarah L Giesy; Martin G Myers; Yves R Boisclair
Journal:  Endocrinology       Date:  2010-05-25       Impact factor: 4.736

4.  Leptin's effect on puberty in mice is relayed by the ventral premammillary nucleus and does not require signaling in Kiss1 neurons.

Authors:  Jose Donato; Roberta M Cravo; Renata Frazão; Laurent Gautron; Michael M Scott; Jennifer Lachey; Inar A Castro; Lisandra O Margatho; Syann Lee; Charlotte Lee; James A Richardson; Jeffrey Friedman; Streamson Chua; Roberto Coppari; Jeffrey M Zigman; Joel K Elmquist; Carol F Elias
Journal:  J Clin Invest       Date:  2010-12-22       Impact factor: 14.808

Review 5.  Hypothalamic pathways linking energy balance and reproduction.

Authors:  Jennifer W Hill; Joel K Elmquist; Carol F Elias
Journal:  Am J Physiol Endocrinol Metab       Date:  2008-02-19       Impact factor: 4.310

Review 6.  A critical view of the use of genetic tools to unveil neural circuits: the case of leptin action in reproduction.

Authors:  Carol F Elias
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2013-11-06       Impact factor: 3.619

7.  Lack of AR in LepRb Cells Disrupts Ambulatory Activity and Neuroendocrine Axes in a Sex-Specific Manner in Mice.

Authors:  Alexandra L Cara; Martin G Myers; Carol F Elias
Journal:  Endocrinology       Date:  2020-08-01       Impact factor: 4.736

8.  Leptin signaling regulates glucose homeostasis, but not adipostasis, in the zebrafish.

Authors:  Maximilian Michel; Patrick S Page-McCaw; Wenbiao Chen; Roger D Cone
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-22       Impact factor: 11.205

9.  Androgen receptor antagonism and an insulin sensitizer block the advancement of vaginal opening by high-fat diet in mice.

Authors:  Diana S Brill; Suzanne M Moenter
Journal:  Biol Reprod       Date:  2009-07-15       Impact factor: 4.285

10.  Central Leptin Regulation of Obesity and Fertility.

Authors:  Qingchun Tong; Yong Xu
Journal:  Curr Obes Rep       Date:  2012-12-01
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