Botulinum toxin (A)-induced bone loss is associated with increased blood velocity and reduced vascular bone porosity.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2025 Vol.40(12) p. 1370-1384

Moussa MS, de Vet T, Lebcir N, Zaslansky P, Chalifour LE, Willie BM, Komarova SV

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Abstract

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.

추출된 의학 개체 (NER)

유형영어 표현한국어 / 풀이UMLS CUI출처등장
시술 botulinum toxin 보툴리눔독소 주사 dict 2
해부 bone scispacy 1
해부 blood scispacy 1
해부 femoral scispacy 1
해부 tibial scispacy 1
해부 hindlimb scispacy 1
해부 hindlimbs scispacy 1
해부 cardiac scispacy 1
해부 BTX-injected tibiae scispacy 1
해부 endocortical scispacy 1
해부 limb scispacy 1
합병증 femoral shaft scispacy 1
합병증 lacunar scispacy 1
합병증 hindlimbs scispacy 1
약물 BTX scispacy 1
질환 bone loss C0029453
Osteopenia
scispacy 1
질환 Disuse-induced bone loss scispacy 1
질환 digit abduction scispacy 1
질환 BTX scispacy 1
기타 vascular bone scispacy 1
기타 blood vessel scispacy 1
기타 sciatic nerve scispacy 1
기타 marrow scispacy 1
기타 murine hindlimbs scispacy 1
기타 BTX scispacy 1
기타 C57Bl/6J female scispacy 1
기타 vascular scispacy 1
기타 cortical scispacy 1
기타 trabecular bone scispacy 1
기타 mice scispacy 1
기타 vascular canal scispacy 1
기타 popliteal scispacy 1
기타 saphenous arteries scispacy 1
기타 femoral popliteal arteries scispacy 1

MeSH Terms

Animals; Female; Porosity; Mice, Inbred C57BL; Mice; Tibia; Blood Flow Velocity; Botulinum Toxins, Type A; X-Ray Microtomography; Hindlimb; Bone Resorption; Bone and Bones

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