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During the latter stages of the luteal phase the corpus luteum begins to regress under the effect of PGF<sub>2α</sub>. Normally the concentration of PGF<sub>2α</sub> in arterial blood is relatively low due to extensive metabolism via the lungs. However there is a large concentration gradient from the uterine vein to the ovarian artery resulting in higher concentrations of PGF<sub>2α</sub> than in systemic circulation. If a pregnancy is to remain viable then luteolysis needs to be avoided and this is achieved where concentrations of PGF<sub>2α</sub> remain below a threshold level allowing the corpus luteum to continue to secrete prostaglandin. There are two main factors involved in the regulation of uterine secretions of PGF<sub>2α</sub>; oxytocin secretions from the corpus luteum and molecules secreted by the developing embryo that facilitate the maternal recognition of pregnancy.
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During the latter stages of the luteal phase the corpus luteum begins to regress under the effect of PGF<sub>2α</sub>. Normally the concentration of PGF<sub>2α</sub> in arterial blood is relatively low due to extensive metabolism via the lungs. However there is a large concentration gradient from the uterine vein to the [[Ovary_-_Anatomy_%26_Physiology#Arterial_Supply|ovarian artery]] resulting in higher concentrations of PGF<sub>2α</sub> than in systemic circulation. If a pregnancy is to remain viable then luteolysis needs to be avoided and this is achieved where concentrations of PGF<sub>2α</sub> remain below a threshold level allowing the corpus luteum to continue to secrete prostaglandin. There are two main factors involved in the regulation of uterine secretions of PGF<sub>2α</sub>; oxytocin secretions from the corpus luteum and molecules secreted by the developing embryo that facilitate the maternal recognition of pregnancy.
 
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Oxytocin secretion via the corpus luteum stimulates endometrial production of PGF<sub>2α</sub> and by the end of the luteal phase the concentration of oxytocin and the number of oxytocin recptors within the endometrium allow the production of enough PGF<sub>2α</sub> to breach the threshold level and cause luteolysis. During pregnancy the embryonically produced pregnancy recognition molecules inhibit the secretion of PGF<sub>2α</sub> from the endometrium ensuring that luteolysis cannot occur.
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Oxytocin secretion via the corpus luteum stimulates endometrial production of PGF<sub>2α</sub> and by the end of the luteal phase the concentration of oxytocin and the number of oxytocin recptors within the endometrium allow the production of enough PGF<sub>2α</sub> to breach the threshold level and cause luteolysis. During pregnancy the embryonically produced [[Maternal_Recognition_of_Pregnancy_-_Anatomy_%26_Physiology|pregnancy recognition]] molecules inhibit the secretion of PGF<sub>2α</sub> from the endometrium ensuring that luteolysis cannot occur.
    
===Prostaglandin (PGE<sub>2</sub>)===
 
===Prostaglandin (PGE<sub>2</sub>)===
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