Nowak Beata, Matuszewska Agnieszka, Filipiak Jarosław, Nikodem Anna, Merwid-Ląd Anna, Pieśniewska Małgorzata, Fereniec-Gołębiewska Lidia, Kwiatkowska Joanna, Szeląg Adam
Department of Pharmacology, Wroclaw Medical University, Wrocław, Poland.
Department of Pharmacology, Wroclaw Medical University, Wrocław, Poland.
Adv Med Sci. 2016 Mar;61(1):85-9. doi: 10.1016/j.advms.2015.09.001. Epub 2015 Sep 25.
The purpose of this study was to investigate the influence of selective agonists of the retinoid receptor X (RXR) and the retinoid acid receptor (RAR) on bone metabolism in rats.
Thirty six male Wistar rats were divided into three groups: receiving bexarotene, or tazarotene, or to control group. Serum biochemical markers of bone turnover (osteocalcin - OC, tartrate resistant acid phosphatase 5 - TRACP5b and osteoprotegerin - OPG) and mechanical properties of bones were analyzed.
There was a significant decrease in the femur index value in groups receiving tazarotene and bexarotene on Day 14 (8% and 20% respectively, p=0.0039). On Day 28, 14 days after discontinuation of tazarotene and bexarotene, the difference in femur indexes was still significant (4% for T1-6 and B1-6, p=0.0270). In the bexarotene group an increase in mean plasma osteocalcin level and mean plasma TRACP5b level was detected. In the tazarotene group the mean osteocalcin level remained unchanged and the mean plasma TRACP5b level decreased. An increased yield stress was detected in groups receiving retinoids comparing to controls after 14 days of tazarotene and bexarotene administration.
Although bexarotene and tazarotene administration caused decrease in the femur index, mechanisms responsible for that effect seem to be different. Our results suggest that bexaroten increases bone turnover. On the contrary, tazaroten seems to have inhibitory effect on bone turnover. A counter influence of selective RAR and RXR agonists on the bone turnover might be the reason for inconsistency in results from published research concerning the influence of retinoids on bone metabolism.
本研究旨在探讨维甲酸X受体(RXR)和维甲酸受体(RAR)的选择性激动剂对大鼠骨代谢的影响。
将36只雄性Wistar大鼠分为三组:分别给予贝沙罗汀、他扎罗汀或作为对照组。分析骨转换的血清生化标志物(骨钙素 - OC、抗酒石酸酸性磷酸酶5 - TRACP5b和骨保护素 - OPG)以及骨骼的力学性能。
在第14天,接受他扎罗汀和贝沙罗汀的组中股骨指数值显著降低(分别为8%和20%,p = 0.0039)。在第28天,即停止给予他扎罗汀和贝沙罗汀14天后,股骨指数的差异仍然显著(T1 - 6和B1 - 6组为4%,p = 0.0270)。在贝沙罗汀组中,检测到平均血浆骨钙素水平和平均血浆TRACP5b水平升高。在他扎罗汀组中,平均骨钙素水平保持不变,而平均血浆TRACP5b水平降低。在给予他扎罗汀和贝沙罗汀14天后,与对照组相比,接受维甲酸的组检测到屈服应力增加。
虽然给予贝沙罗汀和他扎罗汀导致股骨指数降低,但其作用机制似乎不同。我们的结果表明,贝沙罗汀增加骨转换。相反,他扎罗汀似乎对骨转换有抑制作用。选择性RAR和RXR激动剂对骨转换的相反影响可能是已发表的关于维甲酸对骨代谢影响的研究结果不一致的原因。