TY - JOUR
T1 - Mating with seminal vesicle-excised male can affect the uterus phospholipid fatty-acids composition during implantation in an experimental mouse model
AU - Fattahi, Amir
AU - Latifi, Zeinab
AU - Darabi, Masoud
AU - Salmassi, Ali
AU - Farzadi, Laya
AU - Shaaker, Maghsood
AU - Mehdizadeh, Amir
AU - Ghasemnejad, Tohid
AU - Roshangar, Leila
AU - Nouri, Mohammad
N1 - Funding Information:
The study was financially supported by the Women’s Reproductive Health Research Center, Tabriz University of Medical Sciences (grant number of 949/14.07.15) and the paper was extracted from PhD dissertation of Amir Fattahi.
Funding Information:
The study was financially supported by the Women's Reproductive Health Research Center, Tabriz University of Medical Sciences (grant number of 949/14.07.15) and the paper was extracted from PhD dissertation of Amir Fattahi.
Publisher Copyright:
© 2019, Brazilian Society of Urology.
PY - 2019
Y1 - 2019
N2 - Purpose: No comprehensive information is available about uterus fatty acid (FA) change during implantation period and possible effects of the seminal vesicle secretion on it. Materials and Methods: In this study, we evaluated FA composition of uterus phospholipids during the implantation period in intact and seminal vesicle-excised (SVX) mated female mice. Forty NMRI female mice were divided into control (mated with intact male) and seminal vesicle excised (SVX)-mated (mated with SVX-male) groups. The phospholipid fatty acids composition was monitored during the first five days of pregnancy using gas chromatography and also implantation rate was evaluated on fifth day of pregnancy. Results: We found that levels of linoleic acid (LNA) and arachidonic acid (ARA) showed a decreasing trend from the first to the third day of pregnancy and then started to increase on the fourth day and peaked on the fifth day. In contrast, the level of saturated FA (SFA) increased on the second and third day of pregnancy compared to the first (p < 0.05) and then decreased on the fourth and fifth. We also found that the seminal vesicle secretion could affect the levels of LNA, ARA, SFA, and PUFA in uterine phospholipids especially on second and third day. Moreover, there was a positive correlation between ARA level and implantation rate in control but not SVX-mated groups. Conclusions: It can be concluded that several uterus FA that have important roles in early pregnancy could be affected by seminal vesicle secretion.
AB - Purpose: No comprehensive information is available about uterus fatty acid (FA) change during implantation period and possible effects of the seminal vesicle secretion on it. Materials and Methods: In this study, we evaluated FA composition of uterus phospholipids during the implantation period in intact and seminal vesicle-excised (SVX) mated female mice. Forty NMRI female mice were divided into control (mated with intact male) and seminal vesicle excised (SVX)-mated (mated with SVX-male) groups. The phospholipid fatty acids composition was monitored during the first five days of pregnancy using gas chromatography and also implantation rate was evaluated on fifth day of pregnancy. Results: We found that levels of linoleic acid (LNA) and arachidonic acid (ARA) showed a decreasing trend from the first to the third day of pregnancy and then started to increase on the fourth day and peaked on the fifth day. In contrast, the level of saturated FA (SFA) increased on the second and third day of pregnancy compared to the first (p < 0.05) and then decreased on the fourth and fifth. We also found that the seminal vesicle secretion could affect the levels of LNA, ARA, SFA, and PUFA in uterine phospholipids especially on second and third day. Moreover, there was a positive correlation between ARA level and implantation rate in control but not SVX-mated groups. Conclusions: It can be concluded that several uterus FA that have important roles in early pregnancy could be affected by seminal vesicle secretion.
UR - http://www.scopus.com/inward/record.url?scp=85071348669&partnerID=8YFLogxK
U2 - 10.1590/S1677-5538.IBJU.2018.0485
DO - 10.1590/S1677-5538.IBJU.2018.0485
M3 - Journal articles
C2 - 30901177
AN - SCOPUS:85071348669
SN - 1677-5538
VL - 45
SP - 825
EP - 833
JO - International Braz J Urol
JF - International Braz J Urol
IS - 4
ER -