Literature DB >> 19620654

Genetic strain and reproductive status affect endometrial fatty acid concentrations.

S Meier1, A J Peterson, M D Mitchell, M Littlejohn, C G Walker, J R Roche.   

Abstract

Poor reproductive performance limits cow longevity in seasonal, pasture-based dairy systems. Few differences in ovarian dynamics have been reported in different strains of Holstein-Friesian cows, implying that the uterine environment may be a key component determining reproductive success. To test the hypothesis that the uterine environment differs among genetic strains of the Holstein-Friesian cow, endometrial fatty acids (FA) were analyzed from New Zealand (NZ), and North American (NA) Holstein-Friesian cows. The effect of reproductive status was also investigated, with cows from both Holstein-Friesian strains slaughtered on either d 17 of the estrous cycle (termed cyclic) or d 17 of pregnancy (after embryo transfer; termed pregnant). Endometrial tissues were collected from 22 cows (NZ pregnant, n = 6; NZ cyclic, n = 4; NA pregnant, n = 6; NA cyclic, n = 6), and FA composition was analyzed. Daily plasma progesterone concentrations, milk production, milk FA composition, body weight, and body condition score were determined. Milk yield (4% fat-corrected milk) was similar for the NZ (28.5 kg/d) and NA (29.3 kg/d; SE 2.07 kg/d) cows, but NZ cows had a greater mean milk fat percentage. Mean plasma progesterone concentrations were significantly greater in NZ cows. Plasma progesterone concentrations were similar in the pregnant and cyclic groups. Mean length of the trophoblast recovered from the pregnant cows (NZ: 20.8 +/- 2.84 cm; NA: 27.9 +/- 10.23 cm) was not affected by genetic strain. Endometrial tissues from NZ cows contained greater concentrations of C17:0, C20:3n-3, and total polyunsaturated FA. The endometria from pregnant cows contained greater concentrations of C17:0, C20:2, and C20:3n-6, and less C20:1, C20:2, C20:5n-3. The observed changes in endometrial FA between Holstein-Friesian cows of different genetic origins or reproductive states may reflect differences in endometrial function and may affect reproductive function.

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Year:  2009        PMID: 19620654     DOI: 10.3168/jds.2009-2047

Source DB:  PubMed          Journal:  J Dairy Sci        ISSN: 0022-0302            Impact factor:   4.034


  4 in total

1.  Modulation of the maternal immune system by the pre-implantation embryo.

Authors:  Caroline G Walker; Susanne Meier; Mathew D Littlejohn; Klaus Lehnert; John R Roche; Murray D Mitchell
Journal:  BMC Genomics       Date:  2010-08-13       Impact factor: 3.969

2.  Mating with seminal vesicle-excised male can affect the uterus phospholipid fatty-acids composition during implantation in an experimental mouse model.

Authors:  Amir Fattahi; Zeinab Latifi; Masoud Darabi; Ali Salmassi; Laya Farzadi; Maghsood Shaaker; Amir Mehdizadeh; Tohid Ghasemnejad; Leila Roshangar; Mohammad Nouri
Journal:  Int Braz J Urol       Date:  2019 Jul-Aug       Impact factor: 1.541

3.  Physiological and cellular requirements for successful elongation of the preimplantation conceptus and the implications for fertility in lactating dairy cows.

Authors:  Eduardo de Souza Ribeiro; José Felipe Warmling Spricigo; Murilo Romulo Carvalho; Elvis Ticiani
Journal:  Anim Reprod       Date:  2018-08-03       Impact factor: 1.810

4.  Evaluation of real-time PCR endogenous control genes for analysis of gene expression in bovine endometrium.

Authors:  Caroline G Walker; Susanne Meier; Murray D Mitchell; John R Roche; Mathew Littlejohn
Journal:  BMC Mol Biol       Date:  2009-11-01       Impact factor: 2.946

  4 in total

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