METHODS: University students from Jiangsu Province participated in this study. Participants completed self-report surveys assessing emotion regulation strategies. It was conducted from May 2022 to July 2022. The study employed confirmatory factor analysis (CFA) to assess the two-factor model of ERQ-8 and measurement invariance across male and female samples.
RESULTS: The mean age of 1534 participants was 19.83 years (SD = 1.54), and the majority were female (70.4%). The initial ERQ-10 model with ten items demonstrated good fit for all indicators, CFI (Comparative Fit index) = 0.967, TLI (Tucker-Lewis Index) = 0.957, RMSEA (Root Mean Square Error of Approximation) = 0.043, SRMR (Standardised Root Mean Square Residual) = 0.029. However, to assess the fit of the previously proposed ERQ-8 model, two items (Q1 and Q3) were excluded. The fit of the ERQ-8 model was further improved (CFI = 0.989, TLI = 0.984, RMSEA = 0.029, SRMR = 0.021). All item loadings exceeded or were equal to 0.573. Internal consistency analysis based on the ERQ-8 model revealed Cronbach's alpha values of 0.840 for reappraisal and 0.745 for suppression, and corresponding composite reliability (CR) values of 0.846 and 0.747, respectively. Test-retest reliability, assessed using the intraclass correlation coefficient (ICC) (95% CI) within a one-week interval, ranged from 0.537 to 0.679. The correlation coefficient between the two factors was 0.084, significantly below 0.85, which suggested a low correlation between the two factors. The results of the invariance analysis across gender demonstrated that the values of ΔCFI and ΔTLI were both below 0.01. It was supported the gender invariance of the ERQ-8 among university students.
CONCLUSION: The eight-item ERQ demonstrated validity and reliability in evaluating emotion regulation strategies, and measurement invariance was observed across gender among university students. The ERQ-8 may prove to be a practical and cost-effective tool, particularly in time-constrained situations.
AIM: This study aimed to compare the protein profiles of seminal plasma and sperm in Bali and Wagyu cattle and evaluate their correlation with fresh semen quality.
METHODS: The study was conducted at the Singosari National Artificial Insemination Center using 3 Bali and 3 Wagyu superior bulls aged 5-12 years. Sperm motility parameters were analyzed using computer-assisted sperm analysis (IVOS-Hamilton). Sperm were extracted using the PRO-PREPTM Protein Extraction Solution. Sperm and seminal plasma protein concentrations were measured using the BCA protein assay, and 1D SDS-PAGE was used to analyze protein profiles. The gels were stained with Coomassie Brilliant Blue to visualize protein bands.
RESULTS: Comparative analysis of semen characteristics, motility parameters, and kinematic parameters between Wagyu and Bali bulls revealed no significant differences. The seminal plasma protein concentrations in Bali bulls and Wagyu did not show a statistically significant difference. The sperm protein concentration in Bali bulls was significantly higher compared to Wagyu. Seminal plasma analysis of Bali bulls showed a diverse protein profile and Wagyu semen plasma had fewer bands, reflecting breed-specific differences. In contrast, sperm analysis of Bali bulls and Wagyu consistently showed heavy protein bands on sperm function and viability.
CONCLUSION: Bali bulls showed greater variation in spermatozoa protein than Wagyu, with protein differences at molecular weights of 60-63 kDa, 35 kDa, and 18-20 kDa. In addition, a positive correlation was found between the number of motile spermatozoa and the number of straws per ejaculate.
MATERIALS AND METHODS: A bovine single nucleotide polymorphism (SNP) 50K BeadChip was used for the investigation. A total of 46. Sumatran native cattle of three colors as follows: Brown (36 animals), white (9 animals), and black (1 animal), were used as experimental animals.
RESULTS: Results showed that the SNP markers ARS-BFGL-NGS-75486 (p = 2.46 × 10-7) and BTB-01992588 (p = 1.06 × 10-5) were selected as two genetic markers for coat color variation in animals under study, which were located at the cytoplasmic FMR1-interacting protein 2 (CYFIP2) gene at BTA7 and small G protein signaling modulator 1(SGSM1) genes at BTA17, respectively. The polymorphic informative content values of both SNP markers were 0.33 (ARS-BFGL-NGS-75486) and 0.13 (BTB-01992588). In this study, a genetic marker for coat color patterns in Sumatran native cattle was obtained based on the haplotypes of both SNP markers.
CONCLUSION: It can be concluded that CYFIP2 and SGSM1 are two coloration genes that affect the phenotype characteristics of Sumatran native cattle.