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Related Concept Videos

Parkinson's Disease: Treatment01:24

Parkinson's Disease: Treatment

Neurodegenerative disorders, such as Parkinson's Disease (PD), involve the gradual and irreversible destruction of neurons in particular brain areas. These disorders exhibit standard features like proteinopathies, selective vulnerability of some neurons, and an interaction of intrinsic properties, genetics, and environmental influences in neural injury.
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of its...
Antiepileptic Drugs: Potassium Channel Activators01:20

Antiepileptic Drugs: Potassium Channel Activators

Ezocgabine or retigabine, an antiepileptic drug of remarkable efficacy, has revolutionized the management of seizures. It is a potassium channel activator, explicitly targeting the family of Q subtype potassium channels. It enhances the transmembrane potassium currents, regulating neuronal excitability. This action stabilizes the resting membrane potential, a pivotal factor in mitigating the hyperexcitability that characterizes epilepsy.
Ezogabine has gained approval as an adjunctive treatment...
Parkinson Disease l: Introduction01:24

Parkinson Disease l: Introduction

Parkinson’s disease is a chronic, progressive neurodegenerative disorder that primarily affects movement. It is characterized by motor symptoms such as resting tremors, muscle rigidity, bradykinesia (slowness of movement), and postural instability. Patients may notice hand tremors at rest, stiffness during movement, or a shuffling gait. In addition to motor features, non-motor symptoms include sleep disturbances, mood and behavioral changes, constipation, and cognitive impairment, all of which...
Parkinson's Disease: Overview01:15

Parkinson's Disease: Overview

Neurodegenerative disorders are progressive diseases that cause irreversible damage and loss to neurons in specific brain areas. Examples of these disorders include Parkinson's disease, Alzheimer's disease, Multiple Sclerosis (MS), and Amyotrophic Lateral Sclerosis (ALS). These disorders share characteristics such as proteinopathies, selective neuronal vulnerability, and a complex interplay between genetic and environmental factors. The primary therapeutic goal for these conditions is to...
Parkinson Disease ll: Pathophysiology01:24

Parkinson Disease ll: Pathophysiology

Parkinson disease (PD) is a progressive neurodegenerative disorder primarily affecting movement, with additional non-motor features. Its pathophysiology involves complex interactions among genetic susceptibility, environmental exposures, and cellular dysfunction, including dopaminergic neuron loss, protein aggregation, and mitochondrial impairment.Selective NeurodegenerationA key feature is the degeneration of dopaminergic neurons in the substantia nigra pars compacta, leading to reduced...
Alterations in Muscle Tone lll01:11

Alterations in Muscle Tone lll

Rigidity and myotonia are distinct abnormalities of muscle tone that affect resistance and relaxation during movement. Although both involve altered muscle contraction, they arise from different neurological and muscular mechanisms.CharacteristicsRigidity is characterized by uniform resistance to passive movement across the entire range, independent of speed, affecting flexors and extensors equally. It may appear as lead-pipe rigidity (smooth, constant resistance) or cogwheel rigidity...

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Updated: Jul 17, 2026

A Novel Approach to Assess Motor Outcome of Deep Brain Stimulation Effects in the Hemiparkinsonian Rat: Staircase and Cylinder Test
07:14

A Novel Approach to Assess Motor Outcome of Deep Brain Stimulation Effects in the Hemiparkinsonian Rat: Staircase and Cylinder Test

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Zonisamide improves motor function in Parkinson disease: a randomized, double-blind study.

Miho Murata1, Kazuko Hasegawa, Ichiro Kanazawa

  • 1Department of Neurology, Musashi Hospital, National Center of Neurology and Psychiatry, 4-1-1 Ogawahigashimachi, Kodaira, Tokyo 187-8551, Japan. mihom@ncnp.go.jp

Neurology
|January 4, 2007
PubMed
Summary

Zonisamide (ZNS) effectively reduced Parkinson disease (PD) symptoms and "off" time when used with levodopa. Doses of 25-50 mg showed efficacy, with good safety profiles at 25-50 mg.

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Controlling Parkinson's Disease With Adaptive Deep Brain Stimulation
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Controlling Parkinson's Disease With Adaptive Deep Brain Stimulation

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Last Updated: Jul 17, 2026

A Novel Approach to Assess Motor Outcome of Deep Brain Stimulation Effects in the Hemiparkinsonian Rat: Staircase and Cylinder Test
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A Novel Approach to Assess Motor Outcome of Deep Brain Stimulation Effects in the Hemiparkinsonian Rat: Staircase and Cylinder Test

Published on: May 31, 2016

Controlling Parkinson's Disease With Adaptive Deep Brain Stimulation
11:12

Controlling Parkinson's Disease With Adaptive Deep Brain Stimulation

Published on: July 16, 2014

Area of Science:

  • Neurology
  • Pharmacology

Background:

  • Parkinson disease (PD) management often requires adjunctive therapies to levodopa.
  • Optimizing treatment for PD patients with insufficient levodopa response is crucial.

Purpose of the Study:

  • To assess the efficacy, safety, and tolerability of zonisamide (ZNS) as an add-on therapy in Parkinson disease (PD) patients.
  • Investigate the effects of daily zonisamide doses (25, 50, 100 mg) on PD symptoms and motor fluctuations.

Main Methods:

  • A multicenter, randomized, double-blind, placebo-controlled trial was conducted in Japan.
  • Patients received levodopa plus placebo or zonisamide (25, 50, 100 mg/day) for 12 weeks.
  • Primary endpoint: change in Unified Parkinson's Disease Rating Scale (UPDRS) Part III score; secondary endpoints included "off" time and UPDRS Parts I, II, IV, and Modified Hoehn and Yahr Scale.

Main Results:

  • Significant improvement in UPDRS Part III scores was observed in the 25-mg and 50-mg zonisamide groups compared to placebo.
  • Reduced daily "off" time was noted in the 50-mg and 100-mg zonisamide groups.
  • Zonisamide did not increase dyskinesia, and adverse event incidence was similar for 25-mg, 50-mg, and placebo groups, but higher in the 100-mg group.

Conclusions:

  • Zonisamide is a safe and effective adjunctive treatment for Parkinson disease (PD) at daily doses of 25 to 100 mg.
  • The drug is well-tolerated, offering benefits in motor symptom control and reducing "off" time in PD patients.
  • Zonisamide demonstrates a favorable risk-benefit profile for managing Parkinson disease symptoms.