Effects of concanavalin A on the progesterone production by bovine steroidogenic luteal cells in vitro
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Destro, F. C.
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Univ Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, BrazilUniv Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, Brazil
Destro, F. C.
[1
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Martin, I.
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Univ Uberaba Uniube, Univ Uberaba, Uberaba, MG, BrazilUniv Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, Brazil
Martin, I.
[2
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Landim-Alvarenga, F. D. C.
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Univ Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, BrazilUniv Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, Brazil
Landim-Alvarenga, F. D. C.
[1
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Ferreira, J. C. P.
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Univ Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, BrazilUniv Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, Brazil
Ferreira, J. C. P.
[1
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Pate, J. L.
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Penn State Univ, Dept Anim Sci, University Pk, PA 16802 USAUniv Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, Brazil
Pate, J. L.
[3
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机构:
[1] Univ Estadual Paulista Julio de Mesquita Filho UN, FMVZ, Dept Anim Reprod & Vet Radiol, Sao Paulo, Brazil
[2] Univ Uberaba Uniube, Univ Uberaba, Uberaba, MG, Brazil
[3] Penn State Univ, Dept Anim Sci, University Pk, PA 16802 USA
The aim of this study was to evaluate the effects of concanavalin A (CONA) on the progesterone (P4) production by bovine steroidogenic luteal cells (LCs) in vitro. Luteal cells were collected during the mid-luteal stage (at 10-12 days following ovulation) and processed in the laboratory. Luteal cells were grown for 7 days in a humid atmosphere with 5% CO2, with or without 10% foetal bovine serum, and were subjected to the following treatments: control: no treatment; CONA (10 mu g/ml); LH (100 mu g/ml); CONA + LH; LH (100 mu g/ml) + prostaglandin F2 alpha (PGF2 alpha) (10 ng/ml); CONA + LH + PGF2 alpha. Samples of the culture media were collected on days 1 (D1) and 7 (D7) for P4 quantification. The cells were counted on D7 of culture. Differences between treatments were considered statistically significant at p <.05. Culture in the presence of CONA decreased the P4-secreting capacity of LCs on D7 of culture, particularly in the absence of serum. The cell numbers did not change between treatments.