Literature DB >> 2630543

Annual changes in the number, testosterone content and ultrastructure of glandular tissue cells of the testis in the marbled newt Triturus marmoratus.

B Fraile1, R Paniagua, M C Rodríguez, F J Sáez, A Jimenez.   

Abstract

The testes of 8 specimens of Triturus marmoratus were collected during each month of 1987 and processed for electron microscopy and light microscopy demonstration of testosterone (T) following the ABC (avidin-biotin peroxidase complex) method. According to their staining affinity for anti-T antibodies, the glandular tissue cells were classified as T-, T+, T++, and T and the annual changes in the numbers of these cell populations, as well as in the volume occupied by the glandular tissue, were calculated. The volume occupied by the glandular tissue increases from September to December; it begins to decrease in April and disappears from June to August. The glandular tissue is formed from the interstitial cells that surround the lobules containing differentiating germ cells. During the spermatogenic process, the interstitial cells do not show staining affinity for anti-T antibodies. In August-September, the interstitial cells around the lobules that have completed spermatogenesis become positively stained (T+) and form the glandular tissue when the spermatozoa leave the testis. The numbers of intensely stained cells in the glandular tissue (T++ and T ) increase from September to November; begin to decrease in December; disappear in January-February; increase again in March and decrease again in April until they disappear in June-September. The interstitial cells, before their transformation in glandular tissue, are ultrastructurally similar to fibroblasts. After their transformation these cells increase in size and develop abundant smooth endoplasmic reticulum, mitochondria with tubular cristae and lipid droplets. This morphological pattern is maintained in the glandular tissue from September to April in spite of the changes in staining affinity during this period.

Entities:  

Mesh:

Substances:

Year:  1989        PMID: 2630543      PMCID: PMC1256822     

Source DB:  PubMed          Journal:  J Anat        ISSN: 0021-8782            Impact factor:   2.610


  11 in total

1.  [BIOCHEMICAL AND HISTOCHEMICAL DEMONSTRATION OF A DELTA 5-3-BETA-HYDROXYSTEROID DEHYDROGENASE IN THE TESTICLE OF THE TRITON PLEURODELES WALTLII MICHAH].

Authors:  P CERTAIN; G COLLENOT; A COLLENOT; R OZON
Journal:  C R Seances Soc Biol Fil       Date:  1964

2.  Hormonal requirements of the different cycles of the seminiferous epithelium during reinitiation of spermatogenesis in long-term hypophysectomized rats.

Authors:  R G Vernon; V L Go; I B Fritz
Journal:  J Reprod Fertil       Date:  1975-01

3.  In vitro metabolism of cholesterol-4- 14 C and testosterone-4- 14 C in testes and fat bodies of Triturus cristatus carnifex.

Authors:  C Lupo de Prisco; C Basile; G Delrio; G Chieffi
Journal:  Comp Biochem Physiol B       Date:  1972-01-15

4.  Long day photoperiods and temperature of 20 degrees C induce spermatogenesis in blinded and non-blinded marbled newts during the period of testicular quiescence.

Authors:  B Fraile; R Paniagua; M C Rodriguez
Journal:  Biol Reprod       Date:  1988-10       Impact factor: 4.285

5.  Paracrine regulation of Leydig cells by the seminiferous tubules.

Authors:  A Bergh
Journal:  Int J Androl       Date:  1983-02

6.  A fine-structural study of interstitial cell changes in the testes of Necturus maculosus during a portion of the annual cycle, and possible evidence for local feedback control by seminiferous epithelium.

Authors:  A A Ucci
Journal:  Am J Anat       Date:  1982-09

7.  Changes in surface area and number of Leydig cells in relation to the 6 stages of the cycle of the human seminiferous epithelium.

Authors:  R Paniagua; M C Rodríguez; M Nistal; B Fraile; J Regadera; P Amat
Journal:  Anat Embryol (Berl)       Date:  1988

8.  Morphometric studies on rat seminiferous tubules.

Authors:  T Y Wing; A K Christensen
Journal:  Am J Anat       Date:  1982-09

9.  Annual cycle of plasma androgens and testicular composition in the rough-skinned newt, Taricha granulosa.

Authors:  J L Specker; F L Moore
Journal:  Gen Comp Endocrinol       Date:  1980-11       Impact factor: 2.822

10.  Organization of interstitial tissue in the testis of the salamander Necturus maculosus (Caudata:Proteidae).

Authors:  J Pudney; G V Callard
Journal:  J Morphol       Date:  1984-07       Impact factor: 1.804

View more
  5 in total

Review 1.  Testicular structure and germ cells morphology in salamanders.

Authors:  Mari Carmen Uribe; Víctor Mejía-Roa
Journal:  Spermatogenesis       Date:  2015-03-12

2.  Testosterone-immunopositive primordial germ cells in the testis of the bullfrog, Rana catesbeiana.

Authors:  E Sasso-Cerri; E Freymüller; S M Miraglia
Journal:  J Anat       Date:  2005-06       Impact factor: 2.610

Review 3.  Influence of melatonin and photoperiod on animal and human reproduction.

Authors:  A Cagnacci; A Volpe
Journal:  J Endocrinol Invest       Date:  1996-06       Impact factor: 4.256

4.  Carbohydrate moieties of the interstitial and glandular tissues of the amphibian Pleurodeles waltl testis shown by lectin histochemistry.

Authors:  F J Sáez; J F Madrid; R Aparicio; F Hernández; E Alonso
Journal:  J Anat       Date:  2001-01       Impact factor: 2.610

5.  Lifelong testicular differentiation in Pleurodeles waltl (Amphibia, Caudata).

Authors:  Stéphane Flament; Hélène Dumond; Dominique Chardard; Amand Chesnel
Journal:  Reprod Biol Endocrinol       Date:  2009-03-05       Impact factor: 5.211

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.