Serveur d'exploration sur la maladie de Parkinson

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Evolution of Deep Brain Stimulation: Human Electrometer and Smart Devices Supporting the Next Generation of Therapy

Identifieur interne : 000A94 ( Main/Exploration ); précédent : 000A93; suivant : 000A95

Evolution of Deep Brain Stimulation: Human Electrometer and Smart Devices Supporting the Next Generation of Therapy

Auteurs : Kendall H. Lee [États-Unis] ; Charles D. Blaha [États-Unis] ; Paul A. Garris [États-Unis] ; Pedram Mohseni [États-Unis] ; April E. Horne [États-Unis] ; Kevin E. Bennet [États-Unis] ; Filippo Agnesi [États-Unis] ; Jonathan M. Bledsoe [États-Unis] ; Deranda B. Lester [États-Unis] ; Chris Kimble [États-Unis] ; Hoon-Ki Min [Corée du Sud] ; Young-Bo Kim [Corée du Sud] ; Zang-Hee Cho [Corée du Sud]

Source :

RBID : ISTEX:0667351BE39B46F7AF2D5CE4790751E870DEE15A

English descriptors

Abstract

Deep brain stimulation (DBS) provides therapeutic benefit for several neuropathologies, including Parkinson disease (PD), epilepsy, chronic pain, and depression. Despite well‐established clinical efficacy, the mechanism of DBS remains poorly understood. In this review, we begin by summarizing the current understanding of the DBS mechanism. Using this knowledge as a framework, we then explore a specific hypothesis regarding DBS of the subthalamic nucleus (STN) for the treatment of PD. This hypothesis states that therapeutic benefit is provided, at least in part, by activation of surviving nigrostriatal dopaminergic neurons, subsequent striatal dopamine release, and resumption of striatal target cell control by dopamine. While highly controversial, we present preliminary data that are consistent with specific predications testing this hypothesis. We additionally propose that developing new technologies (e.g., human electrometer and closed‐loop smart devices) for monitoring dopaminergic neurotransmission during STN DBS will further advance this treatment approach.

Url:
DOI: 10.1111/j.1525-1403.2009.00199.x


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">Deep brain stimulation (DBS) provides therapeutic benefit for several neuropathologies, including Parkinson disease (PD), epilepsy, chronic pain, and depression. Despite well‐established clinical efficacy, the mechanism of DBS remains poorly understood. In this review, we begin by summarizing the current understanding of the DBS mechanism. Using this knowledge as a framework, we then explore a specific hypothesis regarding DBS of the subthalamic nucleus (STN) for the treatment of PD. This hypothesis states that therapeutic benefit is provided, at least in part, by activation of surviving nigrostriatal dopaminergic neurons, subsequent striatal dopamine release, and resumption of striatal target cell control by dopamine. While highly controversial, we present preliminary data that are consistent with specific predications testing this hypothesis. We additionally propose that developing new technologies (e.g., human electrometer and closed‐loop smart devices) for monitoring dopaminergic neurotransmission during STN DBS will further advance this treatment approach.</div>
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