PMID- 27879456 OWN - NLM STAT- MEDLINE DCOM- 20171219 LR - 20181113 IS - 1573-4935 (Electronic) IS - 0144-8463 (Print) IS - 0144-8463 (Linking) VI - 36 IP - 6 DP - 2016 Dec TI - Hindlimb spasticity after unilateral motor cortex lesion in rats is reduced by contralateral nerve root transfer. LID - 10.1042/BSR20160412 [doi] LID - e00430 AB - Lower extremity spasticity is a common sequela among patients with acquired brain injury. The optimum treatment remains controversial. The aim of our study was to test the feasibility and effectiveness of contralateral nerve root transfer in reducing post stroke spasticity of the affected hindlimb muscles in rats. In our study, we for the first time created a novel animal hindlimb spastic hemiplegia model in rats with photothrombotic lesion of unilateral motor cortex and we established a novel surgical procedure in reducing motor cortex lesion-induced hindlimb spastic hemiplegia in rats. Thirty six rats were randomized into three groups. In group A, rats received sham operation. In group B, rats underwent unilateral hindlimb motor cortex lesion. In group C, rats underwent unilateral hindlimb cortex lesion followed by contralateral L4 ventral root transfer to L5 ventral root of the affected side. Footprint analysis, Hoffmann reflex (H-reflex), cholera toxin subunit B (CTB) retrograde tracing of gastrocnemius muscle (GM) motoneurons and immunofluorescent staining of vesicle glutamate transporter 1 (VGLUT1) on CTB-labelled motoneurons were used to assess spasticity of the affected hindlimb. Sixteen weeks postoperatively, toe spread and stride length recovered significantly in group C compared with group B (P<0.001). H(max) (H-wave maximum amplitude)/M(max) (M-wave maximum amplitude) ratio of gastrocnemius and plantaris muscles (PMs) significantly reduced in group C (P<0.01). Average VGLUT1 positive boutons per CTB-labelled motoneurons significantly reduced in group C (P<0.001). We demonstrated for the first time that contralateral L4 ventral root transfer to L5 ventral root of the affected side was effective in relieving unilateral motor cortex lesion-induced hindlimb spasticity in rats. Our data indicated that this could be an alternative treatment for unilateral lower extremity spasticity after brain injury. Therefore, contralateral neurotization may exert a potential therapeutic candidate to improve the function of lower extremity in patients with spastic hemiplegia. CI - (c) 2016 The Author(s). FAU - Zong, Haiyang AU - Zong H AD - Department of Orthopedic Surgery, Changzheng Hospital, The Second Military Medical University, Shanghai 200003, China. FAU - Ma, Fenfen AU - Ma F AD - Department of Pharmacy, Pudong Hospital, Fudan University, Shanghai 201399, China. FAU - Zhang, Laiyin AU - Zhang L AD - Department of Pharmacy, Linyi People's Hospital, Linyi 276000, China. FAU - Lu, Huiping AU - Lu H AD - Department of Pharmacy, Pudong Hospital, Fudan University, Shanghai 201399, China. FAU - Gong, Jingru AU - Gong J AD - Department of Pharmacy, Pudong Hospital, Fudan University, Shanghai 201399, China. FAU - Cai, Min AU - Cai M AD - Department of Pharmacy, Pudong Hospital, Fudan University, Shanghai 201399, China. FAU - Lin, Haodong AU - Lin H AD - Department of Orthopedic Surgery, Changzheng Hospital, The Second Military Medical University, Shanghai 200003, China. FAU - Zhu, Yizhun AU - Zhu Y AD - Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China zhuyz@fudan.edu.cn yzzhu@must.edu.mo chunlinhou@126.com. AD - State Key Laboratory of Quality Research in Chinese Medicine, Macau University of Science and Technology, Avenida Wai Long, Taipa Macau 999078, China. FAU - Hou, Chunlin AU - Hou C AD - Department of Orthopedic Surgery, Changzheng Hospital, The Second Military Medical University, Shanghai 200003, China zhuyz@fudan.edu.cn yzzhu@must.edu.mo chunlinhou@126.com. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20161223 PL - England TA - Biosci Rep JT - Bioscience reports JID - 8102797 RN - 0 (Slc17a7 protein, rat) RN - 0 (Vesicular Glutamate Transport Protein 1) SB - IM MH - Animals MH - Brain Injuries/chemically induced/*complications MH - Disease Models, Animal MH - Hemiplegia/*etiology/*surgery MH - Hindlimb/*innervation MH - Humans MH - Motor Cortex/*injuries MH - Motor Neurons/physiology MH - Muscle Spasticity/etiology/surgery MH - Muscle, Skeletal/physiology MH - Nerve Regeneration/physiology MH - Rats MH - Rats, Sprague-Dawley MH - Reflex, Abnormal/physiology MH - Spinal Nerve Roots/*surgery MH - Vesicular Glutamate Transport Protein 1/analysis PMC - PMC5180250 OTO - NOTNLM OT - hindlimb OT - motor cortex OT - nerve transfer OT - spasticity EDAT- 2016/11/24 06:00 MHDA- 2017/12/20 06:00 PMCR- 2016/12/01 CRDT- 2016/11/24 06:00 PHST- 2016/09/22 00:00 [received] PHST- 2016/11/21 00:00 [revised] PHST- 2016/11/22 00:00 [accepted] PHST- 2016/11/24 06:00 [pubmed] PHST- 2017/12/20 06:00 [medline] PHST- 2016/11/24 06:00 [entrez] PHST- 2016/12/01 00:00 [pmc-release] AID - BSR20160412 [pii] AID - e00430 [pii] AID - 10.1042/BSR20160412 [doi] PST - epublish SO - Biosci Rep. 2016 Dec 23;36(6):e00430. doi: 10.1042/BSR20160412. Print 2016 Dec.