Dendritic degeneration in neostriatal medium spiny neurons in Parkinson disease
S. Zaja-Milatovic, MS,
D. Milatovic, PhD,
A. M. Schantz, MEd,
J. Zhang, MD, PhD,
K. S. Montine, PhD,
A. Samii, MD,
A. Y. Deutch, PhD and
T. J. Montine, MD, PhD
From the Departments of Pathology (Drs. Milatovic, Zhang, K.S. Montine, and T.J. Montine, S. Zaja-Milatovic and A.M. Schantz) and Neurology (Dr. Samii), University of Washington School of Medicine, Seattle, WA; and Departments of Psychiatry and Pharmacology (Dr. Deutch), Vanderbilt University Medical Center, Nashville, TN.
Address correspondence and reprint requests to Dr. Thomas J. Montine, Department of Pathology, University of Washington, Harborview Medical Center, Box 359791, Seattle, WA 98104; e-mail: tmontine{at}u.washington.edu
Dysfunction of neostriatal medium spiny neurons (MSNs) is hypothesizedto underlie late-stage motor complications of Parkinson disease(PD). The authors demonstrate shortened dendrite length of MSNsthat was similar in four regions of neostriatum in late-stagePD. In contrast, MSN dendrite spine degeneration was unevenlydistributed with the greatest loss in caudal putamen. The authorspropose that these structural changes in MSN may contributeto late-stage motor complications of PD.
Supported by the Nancy and Ellsworth Alvord Endowment, the Cheng-MeiShaw Endowment, and P01 NS044282.
Received July 28, 2004. Accepted in final form September 30,2004.
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