Botulinum toxin injection in murine hindlimbs led to significant bone loss (16% lower cortical thickness and 66% lower trabecular bone volume fraction) and increased blood velocity.
Does botulinum toxin injection alter bone mass and blood flow in murine hindlimbs?
Botulinum toxin-induced paralysis in mice leads to significant bone loss while paradoxically increasing blood velocity in the femoral and popliteal arteries and decreasing vascular porosity.
Disuse-induced bone loss is a common consequence of spaceflight and prolonged bed rest. Intraosseous blood vessel volume and number are decreased in rodents after sciatic nerve resection, and femoral and tibial perfusion and blood flow to the femoral shaft and marrow are reduced after hindlimb unloading. However, it is unclear if alterations in the flow of blood contribute to botulinum toxin (BTX)-induced bone loss. The objective of this study was to assess patterns of tibial bone loss and alterations in blood flow in murine hindlimbs following BTX injection. We hypothesize that flow of blood to the affected hindlimb will diminish along with bone mass and structure. Skeletally mature C57Bl/6J female were injected with BTX (n = 15) or vehicle (n = 14). Paralysis was confirmed using digit abduction, wire hang tests, and activity analysis. In vivo microCT and ex vivo synchrotron tomography were used to assess bone mass, microstructure, (re)modeling, as well as vascular and lacunar porosity. Blood flow in the hindlimbs and cardiac structure/function was monitored by echocardiography. After 3 wk, BTX-injected tibiae had 16% lower cortical thickness and 66% lower trabecular bone volume fraction compared to baseline. MicroCT-based timelapse morphometry showed bone loss was predominantly at endocortical surfaces. Bone loss in the contralateral limb was coincident with reduced rearing capability of BTX-injected mice compared to vehicle controls. Bony vascular canal thickness and surface area were reduced, but there was no change in lacunar properties due to BTX. In vivo ultrasound demonstrated increased velocity time integral for blood flow due to BTX injection in femoral and popliteal but not in saphenous arteries. Thus, BTX led to significant bone loss in hindlimbs, while increasing blood velocity in the femoral popliteal arteries and decreasing vascular porosity. The vascular response to BTX differs from what has been observed in other hindlimb unloading models.
Moussa et al. (Wed,) conducted a other in Disuse-induced bone loss (n=29). Botulinum toxin (BTX) vs. Vehicle was evaluated on Patterns of tibial bone loss and alterations in blood flow. Botulinum toxin injection in murine hindlimbs led to significant bone loss (16% lower cortical thickness and 66% lower trabecular bone volume fraction) and increased blood velocity.