Role of Candidate Genes Regulating Uterine Prostaglandins Biosynthesis for Maternal Recognition of Pregnancy in Domestic Animals

Author:

Kumar Rohit12,Ramteke P. W.1,Nath Amar3,Pramod R. Kumar2,Singh Satyendra P.4,Sharma Sanjeev Kumar2,Kumar Sandeep5

Affiliation:

1. Sam Higginbottom Institute of Agriculture, Technology & Sciences, Allahabad 211007, India

2. Animal Genetics Division, Indian Veterinary Research Institute, Izatnagar, Bareilly 243122, India

3. Division of Surgery, Indian Veterinary Research Institute, Izatnagar, Bareilly 243122, India

4. Department of Animal Genetics and Breeding, College of Veterinary Science and Animal Husbandry, DUVASU, Mathura 281001, India

5. Animal Nutrition Division, Indian Veterinary Research Institute, Izatnagar, Bareilly 243122, India

Abstract

The survivability and opportunity of successful development of an embryo are influenced directly or indirectly by factors controlling uterine microenvironment. Out of all factors, hormones such as prostaglandins (PGs) released during the preimplantation period influence molecular interactions involved in maintenance of pregnancy through reciprocal interactions between the conceptus and endometrium. PGs are important regulators of female reproductive functions, namely, ovulation, uterine receptivity, implantation, and parturition. Among different classes of PGs, prostaglandin F2α (PGF2α) and prostaglandin E2 (PGE2) are main prostanoids produced by human and bovine endometrium for successful growth and development of the posthatching blastocyst. In ruminants, PGF2α produced by endometrium is the major luteolytic agent, whereas PGE2 has luteoprotective and antiluteolytic properties. Therefore, the development and maintenance of the corpus luteum (CL), as well as establishment of pregnancy, depend on the balance of luteolytic PGF2α and luteotropic PGE2. In this review, we discussed the expression and function of genes which predominantly regulate the synthesis and their secretion of PGF2α and PGES, namely, PGFS (AKR1B5/AKR1C3), PGES, PGFR, and COX-2.

Publisher

Hindawi Limited

Subject

General Medicine

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