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

被引:47
作者
Lee, Kendall H. [1 ]
Blaha, Charles D. [2 ]
Garris, Paul A. [3 ]
Mohseni, Pedram [4 ]
Horne, April E. [5 ]
Bennet, Kevin E. [5 ]
Agnesi, Filippo [6 ]
Bledsoe, Jonathan M. [1 ]
Lester, Deranda B. [2 ]
Kimble, Chris [5 ]
Min, Hoon-Ki [7 ]
Kim, Young-Bo [7 ]
Cho, Zang-Hee [7 ]
机构
[1] Mayo Clin, Dept Neurosurg & Physiol & Biomed Engn, Rochester, MN 55905 USA
[2] Univ Memphis, Dept Psychol, Memphis, TN 38152 USA
[3] Illinois State Univ, Dept Biol Sci, Normal, IL 61761 USA
[4] Case Western Reserve Univ, Dept Elect Engn & Comp Sci, Cleveland, OH 44106 USA
[5] Mayo Clin, Div Engn, Rochester, MN 55905 USA
[6] Mayo Clin, Dept Physiol & Biomed Engn, Rochester, MN 55905 USA
[7] Gachon Univ Med & Sci, Neurosci Res Inst, Inchon, South Korea
来源
NEUROMODULATION | 2009年 / 12卷 / 02期
关键词
Deep brain stimulation; Parkinson disease; subthalamic nucleus; voltammetry; wireless integrated circuit; HIGH-FREQUENCY STIMULATION; INTRACRANIAL SELF-STIMULATION; STRIATAL DOPAMINERGIC METABOLISM; SUBTHALAMIC NUCLEUS STIMULATION; OBSESSIVE-COMPULSIVE DISORDER; CARBON-FIBER MICROELECTRODE; VENTRAL TEGMENTAL AREA; NIGRA PARS RETICULATA; RAT CAUDATE-PUTAMEN; PARKINSONS-DISEASE;
D O I
10.1111/j.1525-1403.2009.00199.x
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:85 / 103
页数:19
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