Chanet Audrey, Salles Jérôme, Guillet Christelle, Giraudet Christophe, Berry Alexandre, Patrac Véronique, Domingues-Faria Carla, Tagliaferri Camille, Bouton Katia, Bertrand-Michel Justine, Van Dijk Miriam, Jourdan Marion, Luiking Yvette, Verlaan Sjors, Pouyet Corinne, Denis Philippe, Boirie Yves, Walrand Stéphane
Université Clermont Auvergne, INRA, UNH, CRNH Auvergne, F-63000 Clermont-Ferrand, France.
IFR30, Inserm U563, CHU Purpan, Toulouse F-31024, France.
J Nutr Biochem. 2017 Aug;46:30-38. doi: 10.1016/j.jnutbio.2017.02.024. Epub 2017 Apr 8.
We investigated the impact of vitamin D deficiency and repletion on muscle anabolism in old rats. Animals were fed a control (1 IU vitamin D/g, ctrl, n=20) or a vitamin D-depleted diet (VDD; 0 IU, n=30) for 6 months. A subset was thereafter sacrificed in the control (ctrl6) and depleted groups (VDD6). Remaining control animals were kept for 3 additional months on the same diet (ctrl9), while a part of VDD rats continued on a depleted diet (VDD9) and another part was supplemented with vitamin D (5 IU, VDS9). The ctr16 and VDD6 rats and the ctr19, VDD9 and VDS9 rats were 21 and 24 months old, respectively. Vitamin D status, body weight and composition, muscle strength, weight and lipid content were evaluated. Muscle protein synthesis rate (fractional synthesis rate; FSR) and the activation of controlling pathways were measured. VDD reduced plasma 25(OH)-vitamin D, reaching deficiency (<25 nM), while 25(OH)-vitamin D increased to 118 nM in the VDS group (P<.0001). VDD animals gained weight (P<.05) with no corresponding changes in lean mass or muscle strength. Weight gain was associated with an increase in fat mass (+63%, P<.05), intramyocellular lipids (+75%, P<.05) and a trend toward a decreased plantaris weight (-19%, P=.12). Muscle FSR decreased by 40% in the VDD group (P<.001), but was restored by vitamin D supplementation (+70%, P<.0001). Such changes were linked to an over-phosphorylation of eIF2α. In conclusion, vitamin D deficiency in old rats increases adiposity and leads to reduced muscle protein synthesis through activation of eIF2α. These disorders are restored by vitamin D supplementation.
我们研究了维生素D缺乏和补充对老年大鼠肌肉合成代谢的影响。将动物分为两组,一组喂食对照饮食(每克含1 IU维生素D,对照组,n = 20),另一组喂食维生素D缺乏饮食(VDD组;每克含0 IU,n = 30),持续6个月。之后,处死对照组(ctrl6)和VDD组中的一部分动物。其余对照动物继续在相同饮食下饲养3个月(ctrl9),而一部分VDD大鼠继续喂食缺乏维生素D的饮食(VDD9),另一部分则补充维生素D(5 IU,VDS9)。ctrl6和VDD6组大鼠以及ctrl9、VDD9和VDS9组大鼠分别为21和24月龄。评估了维生素D状态、体重和组成、肌肉力量、重量和脂质含量。测量了肌肉蛋白质合成率(分数合成率;FSR)以及调控途径的激活情况。VDD组降低了血浆25(OH)-维生素D水平,达到缺乏状态(<25 nM),而VDS组的25(OH)-维生素D水平增加到118 nM(P<0.0001)。VDD组动物体重增加(P<0.05),但瘦体重或肌肉力量无相应变化。体重增加与脂肪量增加(+63%,P<0.05)、肌内脂质增加(+75%,P<0.05)以及比目鱼肌重量下降趋势(-19%,P = 0.12)有关。VDD组肌肉FSR下降了40%(P<0.001),但补充维生素D后得以恢复(+70%,P<0.0001)。这些变化与eIF2α的过度磷酸化有关。总之,老年大鼠维生素D缺乏会增加肥胖,并通过激活eIF2α导致肌肉蛋白质合成减少。补充维生素D可恢复这些紊乱。