Regular ArticleBioactive Lysophospholipids and Their G Protein-Coupled Receptors
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2017, TheriogenologyCitation Excerpt :In addition, DP (LPA2R) or OMPT (LPA3R) agonists did not inhibit progesterone secretion by ovine luteal tissue in vitro reported herein indicating that LPA2R or LPA3R agonists are not involved in luteolysis. This is in contrast to reports that luteal mRNA expression of LPA2R increased transiently in bovine and that LPA inhibited LH-stimulated progesterone secretion by these cells in vitro via inhibition of cAMP production [29–31]. Instead, DP (LPA2R) may enhance luteal function, since the LPA2R agonist in vivo increased luteal mRNA expression of LHR, and OMPT the LPA3R agonist did not alter luteal mRNA expression of LHR.
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