Central and peripheral analgesia mediated by the acetylcholinesterase-inhibitor neostigmine in the rat inflamed knee joint model

• Published in: Anesthesia and analgesia Vol. 86; no. 5; pp. 1027 - 1032
• Main Authors: BUERKLE, H, BOSCHIN, M, MARCUS, M. A. E, BRODNER, G, WÜSTEN, R, VAN AKEN, H
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott 01-05-1998
• Subjects: Analgesics; Analgesics, Non-Narcotic - pharmacology; Animals; Arthritis - drug therapy; Biological and medical sciences; Cholinesterase Inhibitors - pharmacology; Dose-Response Relationship, Drug; Injections, Spinal; Knee Joint; Male; Medical sciences; Neostigmine - administration & dosage; Neostigmine - pharmacology; Neuropharmacology; Pharmacology. Drug treatments; Rats; Rats, Sprague-Dawley; Knee; Rat; Enzyme; Neostigmine bromide; Rodentia; Diseases of the osteoarticular system; Enzyme inhibitor; Esterases; Inflammation; Intrathecal administration; Cholinesterase; Carboxylic ester hydrolases; Hyperalgesia; Analgesia; Vertebrata; Chemotherapy; Mammalia; Analgesic; Pain; Treatment; Intraarticular administration; Animal; Hydrolases; Anticholinesterase agent
• ISSN: 0003-2999; 1526-7598
• DOI: 10.1097/00000539-199805000-00023

Intrinsic cholinergic inhibitory pathways present a key modulating system in pain perception. The use of intrathecal (i.t.) acetylcholinesterase-inhibitors, such as neostigmine, result in analgesia in both preclinical and clinical models. However, whether i.t. neostigmine suppresses tonic persistent pain or has peripheral sites of antinociceptive action has not been determined. Thus, we studied central (i.t.) and peripheral (intraarticular; i.a.) neostigmine in a rat inflamed knee joint model. Inhibition of thermal and mechanical hyperalgesia was assessed over 28 h using a modified Hargreaves box and von Frey hairs, respectively. I.t. neostigmine resulted in a dose-dependent thermal analgesia (50% of maximal effective dose [ED50] 0-4 h: 6.6 microg, 24-28 h: 9.4 microg) and mechanical analgesia (ED50 0-4 h: 3.5 microg, 24-28 h: 4.3 microg). I.t. atropine reversed analgesia by i.t. neostigmine. I.a. neostigmine also resulted in an i.a. atropine reversible dose-dependent increase of thermal analgesia, although it did not exceed 60% of a maximal possible analgesic effect with the largest applied dose (ED50 0-4 h: 76.2 microg, 24-28 h: 140.1 microg). Partial suppression of mechanical hyperalgesia was observed after i.a. neostigmine. We conclude that centrally administered neostigmine modulates thermal and mechanical antinociception in this animal model of inflammatory pain. These data suggest a peripheral site of muscarinic antinociception.
This animal study shows that administration of the acetylcholinesterase-inhibitor neostigmine results in enhanced levels of the endogenous neurotransmitter acetylcholine, which seems to act as one of a group of analgesia-modulating compounds at central and peripheral sites in inflammatory pain.