Peran Cytidine 5'-diphosphocoline dalam Penatalaksanaan Nyeri Neuropatik
Abstract
Abstrak. Riview terhadap mekanisme nyeri neuropatik ini adaJah berdasarkan respon yang sangat kompleks terhadap injuri saraf perifer. Terdapat berbagai kemungkinan mekanise yang mendasari terjadinya nyeri neuropatik tennasuk keterlibatan saraf perifer, medulla spinalis, bahkan otak. Penelitian selanjutnya terhadap mekanisme nyeri neuropatik akan membantu kita dalam mengembangkan obat-obat baru yang bekerja pada target tertentu berdasarkan mekanisme yang terjadi. Sehingga prinsip pengobatan yang bersifat simtomatik akan berubah menjadi pengobatan yang bedasarkan mekanisme atau patobiologinya. Dengan dasar pemikiran tersebut saat ini kita sedang mencoba mengembangkan tentang peran Cytidine 5 '-dipbosphocoline dalam penatalaksanaan nyeri neuropatik._(JKS2010; 1:51-62)
Kata kunci: nyeri neuropatik, mekanisme nyeri neuropatik, penatalaksanaan, Cytidine 5 '- diphosphocoline
Abstract. This brief overview of the known mechanisms of neuropathic pain outlines the complex nature of the responses to a peripheral nerve injury. A unifying hypothesis of a single mechanism of all neuropathic pain is most unlikely to be proven and it is probable that an inter-related portfolio of mechanisms contribute to the generation of neuropathic pain in any given patient, with peripheral, spinal and brain events possibly all playing a role. Further elucidation of mechanisms underlying neuropathy will assist in developing novel targets for drug therapy. It may be possible to improve the ethos of clinical management protocols so that there will be a move away from the current disease based treatment towards symptom or, ultimately, mechanism based therapies. It is a clinical challenge to determine which mechanisms may be operating and hence responsible for individual symptomology in each patient. Mechanism based therapy will require a better understanding of mechanisms involved in neuropathic pain and reliable convenient tools for their assessment in the clinic. According to the established mechanisms, we are trying to elaborate the role ofCytidine 5'-diphosphocoline for the treatment ofneuropathic pain. (JKS 2010; 1:51-62)
Keywords: neuropathic pain, NP mechanism, mechanisms based treatment, Cytidine 5'- diphosphocoline
Keywords
References
Daftar Pustaka
W olf 2004
Hogan Q. Role of Decreased Sensory Neuron Membrane Calcium Currents in the Genesis of Neuropathic Pain. Croat Med J. 2007. 48:9-21.
Agut J, Font E, Sacristan A, Ortiz JA.
Bioavailability of Methyl-C CDP- Choline by Oral Route. Drug Res.
33:1045-7.
McCallum et al. Painful peripheral nerve injury decreases calcium current in axotomized sensory neurons. Anesthesiology. 2006.105: 160-8.
D'Orlando KJ, Sandage JrBW.
Citicoline (CDP-choline): mechanisms of action and effects in ischemic brain injury. Neurol Res 1995. 17:281-4.
Hogan Q. Restoration of Calcium Influx Corrects Membrane Hyperexcitability in Injured Rat Dorsal Root Ganglion Neurons. Anesth Analg.2008.107:1045-
.
Levin LA, Peeples P. History of Neuroprotection and Rationale as a Therapy for Glaucoma. Am J Manag Care. 2008. 14:511-4.
Arms K, Camp P: Biology. 41h edition.
New York: Harcourt Brace College
Publishers.
The Cell and The Plasma Membrane.
Available at: http://ecc- book.com/html/cellular membrane.html
Molecular Model of the Nerve Cell
Membrane. Available at:
http://hyperphysics.phy-
astr.gsu edu/Hbase/biology/mempot
Weiss GB. Mini review. Metabolis mandactions of CDP-choline as an Endogenous compound and administered exogenously as citicoline. Life Sci 1995.56: 637- 60.
Chung Mo J, Kim KH, Chung K.
Segmental spinal nerve ligation model of neuropathic pain. In Methodes in molecular medicine; Pain research: Methodes and ptotocols. Humana press Inc. Totowa. 2004. 99 : 38 - 40.
Refbacks
- There are currently no refbacks.