Research Group in Animal Pharmacology of Quebec (GREPAQ), Faculty of Veterinary Medicine, Université de Montréal, C.P. 5000, Saint-Hyacinthe, QC, Canada J2S 7C6.
Evid Based Complement Alternat Med. 2012;2012:646191. doi: 10.1155/2012/646191. Epub 2012 Jul 15.
Objective. The aim of this randomized placebo-controlled trial was to evaluate the beneficial effect of a whole plant extract of Brachystemma calycinum D. Don (BCD) in naturally occurring osteoarthritis (OA) in dogs. Methods. Dogs had stifle/hip OA and poor limb loading based on the peak of the vertically oriented ground reaction force (PVF) measured using a force platform. At baseline, PVF and case-specific outcome measure of disability (CSOM) were recorded. Dogs (16 per group) were then assigned to receive BCD (200 mg/kg/day) or a placebo. The PVF was measured at week (W) 3 and W6. Locomotor activity was recorded throughout the study duration using collar-mounted accelerometer, and CSOM was assessed biweekly by the owner. Results. BCD-treated dogs had higher PVF at W3 and W6 when compared to Baseline (P < 0.001) and at W6 when compared to placebo-treated dogs (P = 0.040). Higher daily duration (P = 0.024) and intensity (P = 0.012) of locomotor activity were observed in BCD-treated dogs compared to baseline. No significant change was observed in either group for CSOM. Conclusions. Treatment with BCD improved the limb impairment and enhanced the locomotor activity in dogs afflicted by naturally-occurring OA. Those preclinical findings provide interesting and new information about the potential of BCD as an OA therapeutic.
本随机安慰剂对照试验的目的是评估 Brachystemma calycinum D. Don(BCD)全植物提取物对犬自然发生的骨关节炎(OA)的有益作用。
根据使用力平台测量的垂直地面反力(PVF)峰值,犬患有膝关节/髋关节 OA 和肢体负重不良。在基线时,记录 PVF 和特定于病例的残疾(CSOM)测量值。然后将狗(每组 16 只)分为 BCD(200mg/kg/天)或安慰剂组。在第 3 周和第 6 周测量 PVF。使用颈圈式加速度计在整个研究期间记录运动活动,主人每两周评估一次 CSOM。
与基线相比,BCD 治疗的犬在第 3 周和第 6 周时的 PVF 更高(P < 0.001),与安慰剂治疗的犬相比,在第 6 周时的 PVF 更高(P = 0.040)。与基线相比,BCD 治疗的犬的每日运动活动时间(P = 0.024)和强度(P = 0.012)更高。在两组中,CSOM 均未观察到显著变化。
BCD 治疗可改善患有自然发生的 OA 的犬的肢体功能障碍并增强其运动活动。这些临床前发现为 BCD 作为 OA 治疗剂的潜力提供了有趣的新信息。