Increased Tumor Necrosis Factor-{alpha} and Prostaglandin E2 Concentrations in the Cerebrospinal Fluid of Rats with Inflammatory Hyperalgesia: The Effects of Analgesic Drugs.

Bianchi M, Martucci C, Ferrario P, Franchi S, Sacerdote P
Increased Tumor Necrosis Factor-{alpha} and Prostaglandin E2 Concentrations in the Cerebrospinal Fluid of Rats with Inflammatory Hyperalgesia: The Effects of Analgesic Drugs. [Journal Article]
Anesth Analg 2007 Apr; 104(4) :949-54.

BACKGROUND: We examined the changes in cerebrospinal fluid (CSF) concentrations of prostaglandin E(2) (PGE(2)) and tumor necrosis factor-alpha (TNF-alpha) after intraplantar administration of complete Freund's adjuvant (CFA) in rats. In addition, we investigated whether different analgesic drugs orally administered at antihyperalgesic doses were able to prevent the changes in PGE(2) and TNF-alpha spinal levels associated with hindpaw inflammation.
METHODS: The Randall-Selitto paw-withdrawal test was used to measure inflammatory hyperalgesia. Tramadol (7.5 mg/kg), paracetamol (65 mg/kg), tramadol plus paracetamol and nimesulide (5 mg/kg) were administered orally twice a day, starting from the first day after the CFA injection. PGE(2) in the CSF was measured by enzyme immunoassay, and TNF-alpha by ELISA. Behavioral and biochemical parameters were measured on Day 7 after intraplantar injection of CFA or saline.
RESULTS: Withdrawal thresholds to mechanical stimuli decreased markedly in the CFA-treated paw. In these animals the quantification of proinflammatory mediators in the CSF revealed a significant increase in both PGE(2) and TNF-alpha concentrations. All the pharmacological treatments prevented the development of the hyperalgesia as well as the PGE(2) increase in the CSF. Conversely, a prevention of the increase in TNF-alpha levels was observed only in rats treated with nimesulide or tramadol and paracetamol in combination.
CONCLUSIONS: Our results demonstrate that peripheral inflammatory hyperalgesia is associated with significant changes of proinflammatory mediators in the CSF. It is important to note, however, that spinal PGE(2) and TNF-alpha proved to be differently affected by pharmacological treatments able to fully abolish the hyperalgesia.