<span><b><span style="font-family:"">Aim: </span></b></span><span><span><span style="font-family:"">Beneficial effects of<b> &l...<span><b><span style="font-family:"">Aim: </span></b></span><span><span><span style="font-family:"">Beneficial effects of<b> </b>virgin coconut oil (VCO) consumption to improve cognition <span>in menopausal females<sup> </sup>remain inconclusive. This study examined the effect of VCO supplementation in aging cycling and non-cycling rodents to assess its impact on cognition. <b>Methods:</b> Sprague-Dawley rats (10</span></span></span></span><span><span><span style="font-family:""> </span></span></span><span><span><span style="font-family:"">-</span></span></span><span><span><span style="font-family:""> </span></span></span><span><span><span style="font-family:"">18 months) were randomly assigned to a supplemented VCO group (SVCO) that received oral doses of 1.42 mL/kg/day VCO (n = 10) and a non-supplemented (</span></span></span><span><span><span style="font-family:"">NVCO) group (n = 10). Their performance in a biased Y-maze discriminative learning paradigm was assessed over a 16-week period. Rats were initially allowed 3 minutes to explore the maze (</span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">habituated</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><span style="font-family:"">) and subsequently </span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">pre-trained</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><i><span style="font-family:""> </span></i></span></span><span><span><span style="font-family:"">in the non-preferred, white chamber to associate the presentation of a tone with a treat (reward). </span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">Training</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><span style="font-family:""> involved 4 daily trials initially for 3 weeks during which rats were rewarded if they entered the white arm within 15 sec after tone presentation. Time (days) to attain at least 75% correct responses (CR) determined acquisition latency (AL). Memory retention (MR1) of the learned task was assessed following a 1-week break from training and absence of supplementation (session T1). Following an additional 2-week break, supplementation of SVCO animals resumed and continued to week 16. In week 14, all animals <span>received </span></span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">re-training</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><span style="font-family:""> for 1 week (session T2) followed by another 1-week break and subsequent assessment of memory (MR2). Vaginal smear cytology determinations were performed throughout the study to identify cycling and non-cycling rats. Student’s t-test and ANOVA with Brown-Forsyt</span></span></span><span><span><span style="font-family:"">he and Tukey’s post-hoc tests were used to compare means. <b>Results: </b>C-<b>S</b>VCO rats attained lower AL, and higher CR and MR scores vs their NVCO counterparts (p < 0.05). At session T2, NC-SVCO rats out-performed other groups (p = 0.048, F = 2.64), attaining highest CR scores between sessions (p = 0.026). <b>Conclusion: </b>VCO supplementation attenuated cognitive decline with a more positive impact on non-cycling rodents suggesting a beneficial effect on brain health in females in menopausal transition.展开更多
文摘<span><b><span style="font-family:"">Aim: </span></b></span><span><span><span style="font-family:"">Beneficial effects of<b> </b>virgin coconut oil (VCO) consumption to improve cognition <span>in menopausal females<sup> </sup>remain inconclusive. This study examined the effect of VCO supplementation in aging cycling and non-cycling rodents to assess its impact on cognition. <b>Methods:</b> Sprague-Dawley rats (10</span></span></span></span><span><span><span style="font-family:""> </span></span></span><span><span><span style="font-family:"">-</span></span></span><span><span><span style="font-family:""> </span></span></span><span><span><span style="font-family:"">18 months) were randomly assigned to a supplemented VCO group (SVCO) that received oral doses of 1.42 mL/kg/day VCO (n = 10) and a non-supplemented (</span></span></span><span><span><span style="font-family:"">NVCO) group (n = 10). Their performance in a biased Y-maze discriminative learning paradigm was assessed over a 16-week period. Rats were initially allowed 3 minutes to explore the maze (</span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">habituated</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><span style="font-family:"">) and subsequently </span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">pre-trained</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><i><span style="font-family:""> </span></i></span></span><span><span><span style="font-family:"">in the non-preferred, white chamber to associate the presentation of a tone with a treat (reward). </span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">Training</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><span style="font-family:""> involved 4 daily trials initially for 3 weeks during which rats were rewarded if they entered the white arm within 15 sec after tone presentation. Time (days) to attain at least 75% correct responses (CR) determined acquisition latency (AL). Memory retention (MR1) of the learned task was assessed following a 1-week break from training and absence of supplementation (session T1). Following an additional 2-week break, supplementation of SVCO animals resumed and continued to week 16. In week 14, all animals <span>received </span></span></span></span><span><span><span style="font-family:""><i></span></span></span><span><span><i><span style="font-family:"">re-training</span></i></span></span><span><span><i><span style="font-family:""></i></span></i></span></span><span><span><span style="font-family:""> for 1 week (session T2) followed by another 1-week break and subsequent assessment of memory (MR2). Vaginal smear cytology determinations were performed throughout the study to identify cycling and non-cycling rats. Student’s t-test and ANOVA with Brown-Forsyt</span></span></span><span><span><span style="font-family:"">he and Tukey’s post-hoc tests were used to compare means. <b>Results: </b>C-<b>S</b>VCO rats attained lower AL, and higher CR and MR scores vs their NVCO counterparts (p < 0.05). At session T2, NC-SVCO rats out-performed other groups (p = 0.048, F = 2.64), attaining highest CR scores between sessions (p = 0.026). <b>Conclusion: </b>VCO supplementation attenuated cognitive decline with a more positive impact on non-cycling rodents suggesting a beneficial effect on brain health in females in menopausal transition.