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  • 11-ketotestosterone  (2)
  • Fast atom bombardment mass spectrometry  (2)
Collection
Keywords
Publisher
Years
  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 1193 (1994), S. 41-47 
    ISSN: 0005-2736
    Keywords: Archaebacterium ; Fast atom bombardment mass spectrometry ; Liposome ; Membrane morphology ; NMR, ^1H- ; Surfactant
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Lipids and Lipid Metabolism 1003 (1989), S. 151-160 
    ISSN: 0005-2760
    Keywords: Archaebacterium ; Fast atom bombardment mass spectrometry ; Liposome ; Membrane morphology ; NMR, ^1H-
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-5168
    Keywords: Bester ; hybrid sturgeon ; testis ; ovary ; steroidogenesis ; 11-ketotestosterone ; 17β-estradial ; 17α ; 20β-dihydroxy-4-pregnen-3-one
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In this study, developmental changes in the steroidogenic capacity of testicular fragments and isolated ovarian follicles of a hybrid sturgeon, Bester, at a variety stage of developments were examined. Testicular fragments or isolated ovarian follicles were incubated in L-15 medium in the presence or absence of different concentrations of five preparations; forskolin, human chorionic gonadotropin (HCG), pregnenolone (P5), 17α-hydroxyprogesterone (17αOHP) and testosterone (T) for 18 h at 15 °C. After incubation, concentrations of 11-ketotestosterone (11 KT) (testis) and, 17β-estradiol (E2) (ovarian follicles) and 17α,20β-dihydroxy-4-pregnen-3-one (DHP) (testis and ovarian follicles) were measured. 11KT was detected in the media following incubation with P5, 17αOHP and T. Its concentration was higher during late spermatogenesis and prespermiation and lower at the degeneration stage. Both P5 and 17αOHP were converted to DHP during the prespermiation stage. Forskolin had little stimulatory effect on the synthesis of 11KT and DHP and HCG did not induce the production of these steroids. E2 was detected in the medium following incubation of follicles with P5, 17αOHP and T at all stages of oocyte development. The concentration of E2 in the medium increased during vitellogenesis with the peak production occurring at the tertiary yolk stage. In contrast, the potencies of follicles to produce steroids shifted to the production of DHP during migratory nucleus stage. Forskolin and HCG had little effect on the synthesis of E2 and DHP. These results demonstrated that the failure of spontaneous spermiation or ovulation is not due to the insufficient synthesis of DHP, but may due to the lack of availability of precursors.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-5168
    Keywords: gonad ; testicular differentiation ; Leydig cell ; Sertoli cell ; human chorionic gonadotropin ; spermatogenesis ; 11-ketotestosterone ; eel ; steroid producing cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The initial appearance and the development of Leydig cells (LCs), the sites of steroid hormone production in the testis, were investigated ultrastructurally during testicular differentiation in the Japanese eel, Anguilla japonica. In addition, the effects of a single injection of human chorionic gonadotropin (HCG; 5 IU g body weight-1) on histological changes of the testes and serum 11-ketotestosterone (11-KT) were examined at various stages (15–18, 20–23, 26–29, 32–35, 38–41 and 46–50 cm body length (BL)) of testicular differentiation. Testicular differentiation was morphologically characterized by the development of loose connective tissue on the medial side in animals 18–29 cm in BL. Ultrastructurally, LCs were first identified in the loose connective tissue of the testis of the 23 cm fish. In the testes of fish over 32 cm, clusters of LCs were distributed throughout the interstitial region accompanying the increase in number of spermatogonia. In fish larger than 32 cm, spermatogenesis was induced by administration of HCG; serum 11-KT levels were also raised. On the other hand, there was no effect on spermatogenesis or serum 11-KT levels in fish less than 29 cm, or in the controls. These result suggests that morphological differentiation of LCs occurs in testis of the 23 cm eel, and subsequently, the testes of eels of BL more than 32 cm acquire the capability to produce steroid hormones.
    Type of Medium: Electronic Resource
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