Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

185 Serum-dependent and serum-independent effects of prolactin and progesterone during the completion of in vitro maturation on metaphase II chromosomes in bovine oocytes

I. Lebedeva A , G. Singina A , E. Shedova A and A. Lopukhov A
+ Author Affiliations
- Author Affiliations

L. K. Ernst Federal Science Center for Animal Husbandry, Podolsk, Russia

Reproduction, Fertility and Development 32(2) 220-221 https://doi.org/10.1071/RDv32n2Ab185
Published: 2 December 2019

Abstract

The final stages of IVM are of great importance for the developmental competence of mammalian oocytes. The goal of the present work was to study effects of prolactin (PRL) and progesterone (PG) during the completion of IVM in serum-containing and serum-free media on destructive and apoptotic changes of MII chromosomes in bovine oocytes. Cumulus-oocyte complexes (COCs) were matured for 16 h in TCM-199 containing 10% fetal calf serum (FCS), 10 μg mL−1 porcine FSH, and 10 μg mL−1 ovine LH at 38.5°C and 5% CO2. Thereafter, the COCs were transferred to and cultured for either 8 or 26 h in the following systems: TCM-199 containing 10% FCS (Control-1) and TCM-199 containing 3 mg mL−1 bovine serum albumin (BSA; Control-2). In both systems, the medium of experimental groups was supplemented with 50 ng mL−1 bovine PRL or 50 ng mL−1 PG. All treatments were repeated 4 to 5 times using 80 to 108 oocytes per group. The state of the oocyte nuclear material was evaluated by Tarkowski's method. Apoptosis in MII oocytes was detected using the terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) method. Arcsine-transformed data were analysed by ANOVA. At the end of culture, the rate of MII oocytes was similar in all the groups (83.4-93.9%). Following 8 h of IVM, the frequency of MII chromosome abnormalities (decondensation, adherence, clumping) was reduced (P < 0.01) in the PRL-1 and PG-1 groups compared with Control-1 (Table 1). This effect was still observed in the PG-1 group (P < 0.001) but disappeared in the PRL-1 group after 26 h of prolonged oocyte culture. In contrast, a decrease in the rate of MII oocytes with abnormal chromosomes occurred only in the PG-2 group by the end of 8 h of culture (P < 0.01), whereas the decrease was revealed in both the PG-2 and PRL-2 groups after 26 h of culture (P < 0.001). Furthermore, the rate of MII oocytes with apoptotic signs following 8 h was lower in the PRL-1 and PG-1 groups than in Control-1 (P < 0.05). During the 26-hculture, this rate increased in all groups, being higher in Control-1 than in the PG-1 group (P < 0.05). The rate of apoptotic oocytes was 2.8 times (8 h) and 1.8 times (26 h) lower in Control-2 than in Control-1 (P < 0.01). Neither PRL nor PG affected oocyte apoptosis in system 2. Thus, during the completion of IVM, PRL can exert a short-term and serum-dependent inhibitory effect on destructive changes of MII chromosomes in bovine oocytes, whereas the similar effect of PG is long-term and serum-independent. Anti-apoptotic effects of both PRL and P4 on the oocytes are determined by serum.


Table 1.  Effects of prolactin (PRL) and progesterone (PG) on MII chromosomes in bovine oocytes
Click to zoom

This study was supported by RFBR (No. 17-29-08035).