Lee Jong In, Kim Hye Won, Rhee Won Ihl, Park Joo Hyun, Lim Seong Hoon, Im Sun, Ko Young Jin
Department of Rehabilitation Medicine, College of Medicine, The Catholic University of Korea, 505 Banpo-Dong, Seocho-Gu, Seoul 137-701, Korea.
Bone. 2006 Aug;39(2):377-82. doi: 10.1016/j.bone.2006.02.055. Epub 2006 Apr 3.
Changes of bone metabolism begin from the initial stages of stroke; therefore, early prevention of these changes has become important. The most appropriate target for preventive therapy is to restrict the profound increase in osteoclastic bone resorption that occur soon after stroke. Oral bisphosphonates, which selectively target osteoclasts and their precursors, are appropriate drugs, but dysphagia or drowsiness after acute stroke can make it difficult to easily administer these compounds to stroke patients. The intravenous (IV) administration of bisphosphonates is an alternative method that can overcome these limitations. In order to determine the effect of IV bisphosphonates at the initial stages of stroke for preventing bone loss, an experiment using ischemic stroke rats was conducted.
Female Sprague-Dawley rats (n = 100) were randomly divided into four separate groups; sham surgery and vehicle-treated group (sham-vehicle), stroke and vehicle-treated group (stroke-vehicle), stroke with low-dose zoledronic acid treatment group (stroke-low) and stroke with high-dose zoledronic acid treatment group (stroke-high). Permanent occlusion of the left middle cerebral artery was performed, resulting in right hemiplegia. The bone mineral density (BMD) of the 4th and 5th lumbar vertebrae and the femur on the stroke side were measured in vivo on the day before stroke and on the 10th and 21st day after stroke. The osteocalcin and carboxy-terminal telopeptide blood levels were measured on the 10th and 21st day after stroke. The BMD of the excised proximal tibia and the maximum load of femoral neck were measured on the 21st day after stroke.
After 21 days of stroke, the BMD of the lumbar vertebrae, femur, and excised tibia and the maximum load of the femoral neck in the sham-vehicle, stroke-low, and stroke-high groups were significantly higher than those in the stroke-vehicle group (P < 0.05). The carboxy-terminal telopeptide levels in the sham-vehicle and stroke-high groups were significantly lower than those in the stroke-vehicle group (P < 0.05).
The results suggest that IV zoledronic acid treatment might prevent bone loss during the initial stages of stroke.
骨代谢变化始于中风的初始阶段;因此,早期预防这些变化变得至关重要。预防性治疗最合适的靶点是限制中风后不久发生的破骨细胞骨吸收的大幅增加。口服双膦酸盐可选择性地作用于破骨细胞及其前体,是合适的药物,但急性中风后的吞咽困难或嗜睡会使向中风患者轻松给药这些化合物变得困难。双膦酸盐的静脉注射是一种可以克服这些限制的替代方法。为了确定静脉注射双膦酸盐在中风初始阶段对预防骨质流失的效果,进行了一项使用缺血性中风大鼠的实验。
将100只雌性Sprague-Dawley大鼠随机分为四组;假手术和溶剂处理组(假手术-溶剂)、中风和溶剂处理组(中风-溶剂)、中风低剂量唑来膦酸治疗组(中风-低)和中风高剂量唑来膦酸治疗组(中风-高)。对左侧大脑中动脉进行永久性闭塞,导致右侧偏瘫。在中风前一天以及中风后第10天和第21天,在体内测量中风侧第4和第5腰椎以及股骨的骨密度(BMD)。在中风后第10天和第21天测量骨钙素和羧基末端肽的血液水平。在中风后第21天测量切除的近端胫骨的BMD和股骨颈的最大负荷。
中风21天后,假手术-溶剂、中风-低和中风-高组的腰椎、股骨、切除胫骨的BMD以及股骨颈的最大负荷均显著高于中风-溶剂组(P<0.05)。假手术-溶剂组和中风-高组的羧基末端肽水平显著低于中风-溶剂组(P<0.05)。
结果表明,静脉注射唑来膦酸治疗可能预防中风初始阶段的骨质流失。