Literature DB >> 21677310

Role of the double luteinizing hormone peak, luteinizing follicles, and the secretion of inhibin for dominant follicle selection in Asian elephants (Elephas maximus).

Imke Lueders1, Kazuyoshi Taya, Gen Watanabe, Yuki Yamamoto, Tatsuya Yamamoto, Saroch Kaewmanee, Cheryl Niemuller, Charlie Gray, Wolf Jürgen Streich, Thomas B Hildebrandt.   

Abstract

Elephants express two luteinizing hormone (LH) peaks timed 3 wk apart during the follicular phase. This is in marked contrast with the classic mammalian estrous cycle model with its single, ovulation-inducing LH peak. It is not clear why ovulation and a rise in progesterone only occur after the second LH peak in elephants. However, by combining ovarian ultrasound and hormone measurements in five Asian elephants (Elephas maximus), we have found a novel strategy for dominant follicle selection and luteal tissue accumulation. Two distinct waves of follicles develop during the follicular phase, each of which is terminated by an LH peak. At the first (anovulatory) LH surge, the largest follicles measure between 10 and 19.0 mm. At 7 ± 2.4 days before the second (ovulatory) LH surge, luteinization of these large follicles occurs. Simultaneously with luteinized follicle (LUF) formation, immunoreactive (ir) inhibin concentrations rise and stay elevated for 41.8 ± 5.8 days after ovulation and the subsequent rise in progesterone. We have found a significant relationship between LUF diameter and serum ir-inhibin level (r(2) = 0.82, P < 0.001). The results indicate that circulating ir-inhibin concentrations are derived from the luteinized granulosa cells of LUFs. Therefore, it appears that the development of LUFs is a precondition for inhibin secretion, which in turn impacts the selection of the ovulatory follicle. Only now, a single dominant follicle may deviate from the second follicular wave and ovulate after the second LH peak. Thus, elephants have evolved a different strategy for corpus luteum formation and selection of the ovulatory follicle as compared with other mammals.

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Year:  2011        PMID: 21677310     DOI: 10.1095/biolreprod.110.090167

Source DB:  PubMed          Journal:  Biol Reprod        ISSN: 0006-3363            Impact factor:   4.285


  5 in total

1.  Gestating for 22 months: luteal development and pregnancy maintenance in elephants.

Authors:  Imke Lueders; Cheryl Niemuller; Peter Rich; Charlie Gray; Robert Hermes; Frank Goeritz; Thomas B Hildebrandt
Journal:  Proc Biol Sci       Date:  2012-06-20       Impact factor: 5.349

2.  Placentation in the African Elephant (Loxodonta africana).

Authors:  W R Twink Allen; Fiona J Stansfield
Journal:  Adv Anat Embryol Cell Biol       Date:  2021       Impact factor: 1.231

3.  Chlorpromazine-Induced Hyperprolactinemia on Rat's Uterus.

Authors:  Zahra Zamani; Samad Zare; Rajabali Sadrkhanlou; Abbas Ahmadi; Elham Movahed
Journal:  Iran Biomed J       Date:  2015-08-04

4.  Cyclic changes in cortisol across the estrous cycle in parous and nulliparous Asian elephants.

Authors:  Kerry V Fanson; Tamara Keeley; Benjamin G Fanson
Journal:  Endocr Connect       Date:  2014-04-15       Impact factor: 3.335

5.  Immunohistochemical localization of inhibin/activin subunits in adult Asian elephant (Elephas maximus) testes.

Authors:  Sirinart Chaichanathong; Kasuyoshi Taya; Gen Watanabe; Kentaro Nagaoka; Worawidh Wajjwalku; Apichaya Sudsukh; Nikorn Thongtip
Journal:  J Vet Med Sci       Date:  2018-01-29       Impact factor: 1.267

  5 in total

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