肉毒毒素和深度大脑刺激在dystonia
Julia Carvalhinho Carlos de Souza1, Ananda Carolina Moraes Falcone1, Renata Montes Garcia Barbosa1
1Movement Disorders Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo 05403-000, Brazil.
Toxins
|June 26, 2024
概括
深度大脑刺激 (DBS) 显著降低了对 dystonia 患者的毒素 (BoNT) 治疗的需要. 这项研究显示,DBS手术后BoNT剂量显著下降,改善了患者管理.
科学领域:
- 神经学 神经学
- 神经外科 神经外科
背景情况:
- 深度大脑刺激 (DBS) 是自2003年以来FDA批准的 dystonia 治疗方法.
- 推使用DBS治疗不对毒素 (BoNT) 等疗法产生反应的 dystonia.
- 长期研究证实了DBS在改善运动功能和生活质量的有效性.
研究的目的:
- 为了评估DBS手术对毒素 (BoNT) 剂量在 dystonia患者的影响.
- 为了确定DBS是否减少了整体BoNT治疗负担.
主要方法:
- 对23名 dystonia 患者的回顾性多中心图表审查.
- 在DBS手术前后对肉毒素 (BoNT) 总剂量和肌肉剂量的分析.
主要成果:
- 在DBS手术后观察到BoNT总剂量的中位数显著减少 (从800到700单位).
- 这种减少代表了中位数BoNT剂量下降12.5%.
- 基线和手术后的平均BoNT剂量差异在随访期间一致.
结论:
- DBS手术可以显著降低泛性 dystonia 患者的肉毒毒素 (BoNT) 剂量.
- 这些发现表明,在成功植入DBS后,对BoNT的依赖性降低了.
相关概念视频
Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin
671
Directly acting muscle relaxants like dantrolene and botulinum toxin (BoNT) have distinct mechanisms and applications. Dantrolene, a hydantoin derivative, acts on the ryanodine receptor (RYR1) in skeletal muscle cells. RYR1 are calcium channels present at the sarcoplasmic reticulum membrane. In response to excitation, they release calcium ions from the sarcoplasmic reticulum to the cytosol. Calcium promotes actin-myosin-mediated contraction of muscles.
The binding of dantrolene to the RYR1...
The binding of dantrolene to the RYR1...
671
Skeletal Muscle Relaxants: Therapeutic Uses
479
Skeletal muscle relaxants are used to relax muscle tone and alleviate painful muscle contractions. However, the choice of skeletal muscle relaxants depends on the duration of the surgical procedure in order to minimize potential side effects. Skeletal muscle relaxants like neuromuscular blocking agents [NMBAs] are commonly employed as adjuvants alongside general anesthetics in clinical settings. NMBAs are also used to maintain controlled ventilation during surgery of the larynx or pharynx...
479
Depolarizing Blockers: Mechanism of Action
1.5K
Depolarizing blockers act on skeletal muscle fibers' membranes and induce their depolarization. Most depolarizing blockers have two quaternary N+ atoms that bind the nicotinic acetylcholine receptors and cause neuromuscular blockade within minutes.
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because...
Succinylcholine is the most commonly used depolarizing blocker. Chemically, it constitutes two molecules of acetylcholine joined together by an acetate methyl group. They act on the receptors in the same way as acetylcholine. Because...
1.5K
Depolarizing Blockers: Pharmocokinetics
317
Depolarizing blockers are administered through intravenous injection. Succinylcholine is the most common choice of depolarizing blockers in emergency clinical practices. Although they have a rapid onset, they readily diffuse away from the motor end plate into the extracellular fluid. They are metabolized by enzymes such as liver butyrylcholinesterase and plasma pseudocholinesterases. This produces a short duration of action, typically 5-10 minutes long, unlike nondepolarizing blockers, which...
317
Classification of Skeletal Muscle Relaxants
2.4K
Skeletal muscle relaxants are a group of drugs that can reduce muscle stiffness and induce temporary paralysis to relieve pain. These agents can act centrally to reduce muscle tone or spasms in painful conditions such as multiple sclerosis (MS), amyotrophic lateral sclerosis (ALS), or spinal injuries; they are called antispasmodics or spasmolytics.
Peripherally acting skeletal muscle relaxants interfere with the neurotransmission at the neuromuscular end plate to induce paralysis during...
Peripherally acting skeletal muscle relaxants interfere with the neurotransmission at the neuromuscular end plate to induce paralysis during...
2.4K
Peripherally and Centrally Acting Muscle Relaxants: A Comparison
3.2K
Skeletal muscle relaxants can target the central nervous system [CNS] to reduce muscle tension or act directly at the neuromuscular junction to induce temporary paralysis. These two classes of muscle relaxants are called centrally acting muscle relaxants and peripherally acting muscle relaxants. They differ in their action, mechanism, administration route, and clinical uses.
Centrally acting muscle relaxants can be further divided into spasmolytic and antispasmodic drugs. Spasmolytic...
Centrally acting muscle relaxants can be further divided into spasmolytic and antispasmodic drugs. Spasmolytic...
3.2K


