Literature DB >> 3282246

Inhibin.

F H De Jong1.   

Abstract

Inhibin has been defined as a gonadal hormone that exerts a specific negative feedback action on the secretion of FSH from the gonadotropic cells of the pituitary gland. The existence of inhibin was postulated as early as 1923 (250). However, only after reliable and sensitive bioassay systems for the detection and estimation of inhibin had been developed and an ample source of inhibin was found in the form of ovarian follicular fluid has progress been made in the isolation and characterization of the hormone. It is apparent now that inhibin, which itself consists of a dimer of two different subunits, alpha and beta, is a member of a much larger family of (glyco)protein hormones and growth factors, which also includes Müllerian-inhibiting substance, transforming growth factor-beta, erythroid differentiation factor, an insect protein that plays an important role in differentiation, and the dimer of two inhibin beta-subunits, activin. The latter substance was reported to counteract the effects of inhibin in pituitary cells. Interactions between these regulatory substances will certainly be a field of major interest in the near future. Inhibin molecules, similar to those in the gonads, have been detected in placental tissue as well. The postulate of inhibin in seminal plasma, prostate, and gastric juice is apparently due to detection of substances that differ from gonadal inhibin. Most likely these substances, the amino acid sequences of which have been elucidated, have a biological function that differs from the suppression of peripheral levels of FSH in vivo. Inhibin is produced in the Sertoli cells in the testis and in the granulosa cells in the ovary. The production of inhibin is stimulated by FSH, but presently a lot of controversy exists about other factors that might play a role in the regulation of the production of inhibin. Because of the lack of reliable methods for estimation of peripheral levels of inhibin in humans and experimental animals, almost all evidence for the physiological importance of inhibin in the regulation of reproductive processes is derived from circumstantial evidence. From these indirect results, it appears likely that inhibin plays an important role in the feedback regulation of peripheral concentrations of FSH during the period in which Sertoli cells and granulosa cells, the target cells for FSH, divide, i.e., during puberty in male animals and during the development of ovarian follicles in female animals.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1988        PMID: 3282246     DOI: 10.1152/physrev.1988.68.2.555

Source DB:  PubMed          Journal:  Physiol Rev        ISSN: 0031-9333            Impact factor:   37.312


  16 in total

1.  Immunization against endogenous inhibin increases normal oocyte/embryo production in adult mice.

Authors:  Mohamed S Medan; Haibin Wang; Gen Watanabe; Akira K Suzuki; Kazuyoshi Taya
Journal:  Endocrine       Date:  2004-07       Impact factor: 3.633

Review 2.  Recent advances in the human physiology of inhibin secretion.

Authors:  D M de Kretser; D M Robertson; G P Risbridger
Journal:  J Endocrinol Invest       Date:  1990 Jul-Aug       Impact factor: 4.256

3.  Identification of transferrin and inhibin-like proteins in matrigel.

Authors:  G Dirami; V Papadopoulos; H K Kleinman; D C Defreese; N A Musto; M Dym
Journal:  In Vitro Cell Dev Biol Anim       Date:  1995-06       Impact factor: 2.416

4.  Human chorionic gonadotropin inhibits proliferation and induces expression of inhibin in human breast epithelial cells in vitro.

Authors:  M V Alvarado; N E Alvarado; J Russo; I H Russo
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-01       Impact factor: 2.416

5.  Placental activin A is required for follicular development during the second half of pregnancy in the golden hamster (Mesocricetus auratus).

Authors:  Chie Furuta; Sayoko Arakawa; Zhanquan Shi; Gen Watanabe; Kazuyoshi Taya
Journal:  Endocrine       Date:  2008-05-20       Impact factor: 3.633

6.  Follicle-stimulating hormone synthesis and fertility depend on SMAD4 and FOXL2.

Authors:  Jérôme Fortin; Ulrich Boehm; Chu-Xia Deng; Mathias Treier; Daniel J Bernard
Journal:  FASEB J       Date:  2014-04-16       Impact factor: 5.191

7.  Genetic evidence that SMAD2 is not required for gonadal tumor development in inhibin-deficient mice.

Authors:  Saneal Rajanahally; Julio E Agno; Roopa L Nalam; Michael B Weinstein; Kate L Loveland; Martin M Matzuk; Qinglei Li
Journal:  Reprod Biol Endocrinol       Date:  2010-06-21       Impact factor: 5.211

8.  CTNNB1 signaling in sertoli cells downregulates spermatogonial stem cell activity via WNT4.

Authors:  Alexandre Boyer; Jonathan R Yeh; Xiangfan Zhang; Marilène Paquet; Aurore Gaudin; Makoto C Nagano; Derek Boerboom
Journal:  PLoS One       Date:  2012-01-12       Impact factor: 3.240

9.  Superovulation using the combined administration of inhibin antiserum and equine chorionic gonadotropin increases the number of ovulated oocytes in C57BL/6 female mice.

Authors:  Toru Takeo; Naomi Nakagata
Journal:  PLoS One       Date:  2015-05-29       Impact factor: 3.240

10.  Human testicular germ cell tumours express inhibin subunits, activin receptors and follistatin mRNAs.

Authors:  R H van Schaik; C D Wierikx; L H Looijenga; J W Oosterhuis; F H de Jong
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

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