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Volume 73, Issue 2, Pages 177-183 (August 2009)


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Combined use of pregabalin and memantine in fibromyalgia syndrome treatment: A novel analgesic and neuroprotective strategy?

Jill M. ReclaabCorresponding Author Informationemail addressemail address, Constantine D. Sarantopouloscd

Received 7 January 2009; accepted 11 January 2009. published online 13 April 2009.

Summary 

Fibromyalgia syndrome (FMS) is a chronic widespread pain syndrome that is estimated to affect 4–8 million US adults. The exact molecular mechanisms underlying this illness remain unclear, rendering most clinical treatment and management techniques relatively ineffective. It is now known that abnormalities in both nociceptive and central pain processing systems are necessary (but perhaps not sufficient) to condition the onset and maintenance of FMS. These same systemic abnormalities are thought to be responsible for the loss of cephalic gray matter density observed in all FMS patients groups studied to date. The current scope of FMS treatment focuses largely on analgesia and does not clearly address potential neuroprotective strategies. This article proposes a combined treatment of pregabalin and memantine to decrease the pain and rate of gray matter atrophy associated with FMS. This dual-drug therapy targets the voltage-gated calcium ion channel (VGCC) and the N-methyl d-aspartate receptor (NMDAR) (respectively), two primary components of the human nociceptive and pain processing systems.

a IGERT Program in Functional Genomics, The University of Maine, Orono ME 04469, United States

b The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609, United States

c Clement J. Zablocki Veterans Affairs Medical Center, Pain Management Center, 5000 West National Avenue, Milwaukee, WI 53295, United States

d Medical College of Wisconsin, Department of Anesthesiology, 8701 Watertown Plank Road, Milwaukee, WI 53226, United States

Corresponding Author InformationCorresponding author. Address: The Jackson Laboratory, 600 Main Street, Bar Harbor, ME 04609, United States. Tel.: +1 207 288 6408.

PII: S0306-9877(09)00169-8

doi:10.1016/j.mehy.2009.01.052


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