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1 Laboratoire de Physiopathologie et Pharmacologie Articulaires, Unite Mixte Recherche 7561 Centre National de la Recherche Scientifique-Université Henri Poincaré-Nancy I and 2 Laboratoire de Physiologie, Faculté de Médecine, Université Henri Poincaré-Nancy I, 54505 Vandoeuvre-lès-Nancy, France
This study was designed
to investigate the pathways involved in neurogenic-mediated articular
cartilage damage triggered by a nonsystemic distant subcutaneous or
intra-articular inflammation. The cartilage damage was assessed 24 h after subcutaneous or intra-articular complete Freund's
adjuvant (CFA) injection measuring patellar proteoglycan (PG) synthesis
(ex vivo [Na235SO4]
incorporation) in 96 Wistar rats. Unilateral subcutaneous or
intra-articular injection of CFA induced significant decrease (25-29%) in PG synthesis in both patellae. Chronic administration of capsaicin (50 mg · kg
1 · day
1 during 4 days), which blunted the normal response of C fiber stimulation,
prevented the bilateral significant decrease in cartilage synthesis.
Similarly, intrathecal injection of MK-801 (10 nmol/day during 5 days),
which blocked the glutamatergic synaptic transmission at the dorsal
horn of signal originating in primary afferent C fibers, eliminated the
CFA-induced PG synthesis decrease in both patellae. Chemical
sympathectomy, induced by guanethidine (12.5 mg · kg
1 · day
1 during 6 wk), also prevented PG synthesis alteration. Finally, compression of
the spinal cord at the T3-T5 level had a similar protective effect on
the reduction of [Na235SO4]
incorporation. It is concluded that the signal that triggers articular
cartilage synthesis damage induced by a distant local inflammation
1) is transmitted through the afferent C fibers, 2) makes glutamatergic synaptic connections with the
preganglionic neurons of the sympathetic system, and 3)
involves spinal and supraspinal pathways.
neurogenic inflammation; proteoglycan synthesis; neural pathways
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