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多柔比星化学性肌切除术治疗颈部肌张力障碍:直接注射入胸锁乳突肌后的组织学评估

Doxorubicin chemomyectomy as a treatment for cervical dystonia: histological assessment after direct injection into the sternocleidomastoid muscle.

作者信息

McLoon L K, Falkenberg J H, Dykstra D, Iaizzo P A

机构信息

Department of Ophthalmology, University of Minnesota, Minneapolis 55455, USA.

出版信息

Muscle Nerve. 1998 Nov;21(11):1457-64. doi: 10.1002/(sici)1097-4598(199811)21:11<1457::aid-mus14>3.0.co;2-y.

Abstract

The sternocleidomastoid muscle (SCM) is one of the major muscles involved in producing abnormal head position in cervical dystonia patients. This study tested whether doxorubicin chemomyectomy, direct injection of doxorubicin into the SCM to permanently remove muscle fibers, has the potential to be a nonsurgical, permanent treatment for cervical dystonia. The right SCM of rabbits was injected with either 1 or 2 mg doxorubicin. Animals were sacrificed 1-2 months postinjection. The SCM was prepared for histological examination of muscle fiber loss and fiber type composition. In all cases, direct injection of doxorubicin resulted in significant decreases in total muscle cross-sectional areas ranging from 75% up to 98%. Individual myofiber cross-sectional areas were smaller than normal after 2 mg doxorubicin treatment, but similar to normal fiber size after 1 mg doxorubicin. There were increased numbers of myofibers that expressed slow and neonatal myosin heavy chain isoforms in these remaining muscle fibers compared to the untreated SCM on the contralateral side. Developmental myosin heavy chain (MHC) was also present in 53% of the remaining myofibers of the treated muscles. The fiber type composition of muscles contralateral to the doxorubicin injections was compared to the fiber type composition of SCM from normal, untreated controls; no difference was seen in the proportions of fast, slow, and neonatal MHC fiber types in these SCM muscles. In summary, the direct injection of doxorubicin into the SCM resulted in significant muscle loss. This supports the use of doxorubicin chemomyectomy as a potential permanent, nonsurgical treatment for cervical dystonia.

摘要

胸锁乳突肌(SCM)是导致颈部肌张力障碍患者头部姿势异常的主要肌肉之一。本研究测试了阿霉素化学去神经术,即将阿霉素直接注射到胸锁乳突肌中以永久性去除肌纤维,是否有可能成为一种治疗颈部肌张力障碍的非手术永久性疗法。给兔的右侧胸锁乳突肌注射1毫克或2毫克阿霉素。在注射后1至2个月处死动物。制备胸锁乳突肌用于肌纤维损失和纤维类型组成的组织学检查。在所有情况下,直接注射阿霉素导致总肌肉横截面积显著减少,减少幅度从75%到98%不等。在2毫克阿霉素治疗后,单个肌纤维横截面积小于正常,但在1毫克阿霉素治疗后与正常纤维大小相似。与对侧未治疗的胸锁乳突肌相比,这些剩余肌纤维中表达慢速和新生儿肌球蛋白重链异构体的肌纤维数量增加。发育型肌球蛋白重链(MHC)也存在于治疗肌肉剩余肌纤维的53%中。将注射阿霉素对侧肌肉的纤维类型组成与正常未治疗对照的胸锁乳突肌纤维类型组成进行比较;在这些胸锁乳突肌中,快速、慢速和新生儿MHC纤维类型的比例没有差异。总之,将阿霉素直接注射到胸锁乳突肌中导致显著的肌肉损失。这支持将阿霉素化学去神经术作为治疗颈部肌张力障碍的一种潜在的永久性非手术疗法。

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