Korean J Anat.  2001 Dec;34(6):653-666.

Morphometric Study of the Effects of Various Analgesic Compound in Experimental Arthritis Model

Affiliations
  • 1Brain Research Institute, Department of Anatomy, College of Medicine, Yonsei University, Korea. kapark@yumc.yonsei.ac.kr
  • 2Department of Neurosurgery, Sangkae Bak Hospital, Korea.
  • 3Department of Anatomy, College of Medicine, Seonam University, Korea.

Abstract

Arthritis is the most common disease of joint in old age and almost all the old human are suffering from arthritis. Arthritis gives so severe pain hard to endure that it can devastate human. But we still do not know where the arthritic pain comes from and the generation mechanism of it. For the study of effects of anti-inflammatory drugs on the c-fos immunoreactive neurons, substance P-and CGRPimmunoreactive neurons in dorsal horn and DRG, cyclooxygenase (COX) inhibitors indomethacin (0.5 mg/kg), piroxicam (0.5 mg/kg), NMDA receptor antagonist MK 801 (2 mg/kg), and capsaicin (50 mg/kg) were administered to the experimental arthritis model. Male Sprague-Dawley rats were used for this study. Arthritis was induced by injection of 4% kaolin followed by 2% carrageenan into the articular capsule of left knee. Two hours, 24 hours and 7 days after injection, animals were sacrificed and processed for imunohistochemical staining for c-fos in spinal dorsal horn, for substance P (SP) and CGRP in DRG. The results were as follows; 1. The number of c-fos immunoreactive neurons were significantly decreased at 2 h after piroxicam and MK-801 administration and 1 week after indomethacin, MK-801 and capsaicin treatment in the inflamed side of dorsal horn. 2. There were the significant decrease of SP-and CGRP-immunoreactive area 2 h after indomethacin administration and 1week after capsaicin treatment in the inflamed side of dorsal horn. 3. The number of SP- and CGRP-immunoreactive neurons in DRG were decreased after drugs administration and no difference is in the degree of effectiveness between drugs. Indomethacin and piroxicam which is an inhibitors of COX, significantly reduced the expression of c-fos proteins and desensitized nociceptive primary afferents at the early time, and capsaicin, a pungent algesic substance, decreased the level of c-fos protein, SP and CGRP over a wider time in dorsal horn and DRG.

Keyword

Cyclooxygenase inhibitor; NMDA receptor antagonist; Capsaicin; c-fos; Substance P; CGRP; Dorsal root ganglia

MeSH Terms

Animals
Arthritis*
Capsaicin
Carrageenan
Diagnosis-Related Groups
Dizocilpine Maleate
Ganglia, Spinal
Horns
Humans
Indomethacin
Joint Capsule
Joints
Kaolin
Knee
Male
N-Methylaspartate
Neurons
Piroxicam
Prostaglandin-Endoperoxide Synthases
Proto-Oncogene Proteins c-fos
Rats, Sprague-Dawley
Substance P
Capsaicin
Carrageenan
Dizocilpine Maleate
Indomethacin
Kaolin
N-Methylaspartate
Piroxicam
Prostaglandin-Endoperoxide Synthases
Proto-Oncogene Proteins c-fos
Substance P
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