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Progesterone receptor-mediated inhibition of apoptosis in granulosa cells isolated from rats treated with human chorionic gonadotropin.

Svensson, Eva Ch (author)
Gothenburg University,Göteborgs universitet,Institutionen för fysiologi och farmakologi,Institute of Physiology and Pharmacology
Markström, Emilia (author)
Gothenburg University,Göteborgs universitet,Institutionen för fysiologi och farmakologi, Avdelningen för fysiologi,Institute of Physiology and Pharmacology, Dept of Physiology
Andersson, M (author)
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Billig, Håkan, 1955 (author)
Gothenburg University,Göteborgs universitet,Institutionen för fysiologi och farmakologi, Avdelningen för fysiologi,Institute of Physiology and Pharmacology, Dept of Physiology
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 (creator_code:org_t)
2000
2000
English.
In: Biology of reproduction. - 0006-3363. ; 63:5, s. 1457-64
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Almost all ovarian follicles undergo atresia during follicular development. However, the number of corpora lutea roughly equals the number of preovulatory follicles in the ovary. Because apoptosis is the cellular mechanism behind follicle and luteal cell demise, this suggests a change in apoptosis susceptibility during the periovulatory period. Sex steroids are important regulators of follicular cell survival and apoptosis. The aim of the present work was to study the role of progesterone receptor-mediated effects in the regulation of granulosa cell apoptosis. The levels of internucleosomal DNA fragmentation were evaluated in rat granulosa cells before and after induction of the nuclear progesterone receptor, using hCG treatment to eCG-primed rats to mimic the naturally occurring LH surge. Granulosa cells isolated from hCG-treated rats showed a several-fold increase in the expression of progesterone receptor mRNA and a 47% decrease (P < 0.01) in DNA fragmentation after 24 h incubation in serum-free medium compared to granulosa cells isolated from rats treated with eCG only. The effect of hCG treatment in vivo was dose-dependently reversed in vitro by addition of antiprogestins (Org 31710 or RU 486) to the culture medium, demonstrated by increased DNA fragmentation as well as increased caspase-3 activity. Addition of antiprogestins to granulosa cells isolated from immature or eCG-treated rats did not result in increased DNA fragmentation. The results suggest that progesterone receptor-mediated effects are involved in regulating the susceptibility to apoptosis in LH receptor-stimulated preovulatory rat granulosa cells.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Fysiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Physiology (hsv//eng)

Keyword

Animals
Apoptosis
physiology
Caspase 3
Caspases
antagonists & inhibitors
metabolism
Cell Differentiation
drug effects
physiology
Cells
Cultured
Chorionic Gonadotropin
pharmacology
DNA Fragmentation
drug effects
Electrophoresis
Polyacrylamide Gel
Enzyme Inhibitors
pharmacology
Female
GABA Antagonists
pharmacology
Granulosa Cells
physiology
Humans
Ovulation
physiology
Rats
Rats
Sprague-Dawley
Receptors
GABA
drug effects
Receptors
LH
drug effects
Receptors
Progesterone
physiology
Reverse Transcriptase Polymerase Chain Reaction

Publication and Content Type

ref (subject category)
art (subject category)

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Svensson, Eva Ch
Markström, Emili ...
Andersson, M
Billig, Håkan, 1 ...
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MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Physiology
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Biology of repro ...
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University of Gothenburg

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