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  • Adjuvant arthritis  (1)
  • Analgesia  (1)
  • Cutaneous afferents  (1)
  • 1
    ISSN: 1432-1106
    Keywords: Key words Nitric oxide ; Adjuvant arthritis ; Chronic inflammation ; Central canal ; Ependymal cell
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Nitric oxide (NO) possibly plays an important role in the events resulting in hyperalgesia. Nitric oxide synthase (NOS) is a key enzyme in the production of NO. In this study, the relationship between NOS and hyperalgesia in a rat chronic arthritis model was tested. Chronic arthritis was induced by injection of incomplete Freund’s adjuvant into the knee joint cavity unilaterally. The paw withdrawal latency (PWL) to radiant heat was used to detect secondary thermal hyperalgesia induced by the arthritis. After 1 day the PWL of the arthritic hindpaw decreased and it reached its nadir at 3 days after induction of arthritis. The lumbar and cervical enlargement of the spinal cord were removed in different groups of animals 3, 7, 14, or 21 days after induction of arthritis, and frozen tissue sections were cut. Two series of sections were incubated with polyclonal antibodies to neuronal NOS (nNOS) or to inducible NOS (iNOS). nNOS was found to increase gradually in laminae I–III in the lumber but not in the cervical enlargement. The change became most obvious 14 days after induction of arthritis as compared to the control animals. Ependymal cells around the central canal of the lumbar enlargement were more densely stained by anti-iNOS after arthritis. A corresponding change was also found in the cervical enlargement. Computer-assisted image analysis revealed that the mean density of the affected areas in the treated group increased significantly compared with the control animals. This study suggests that the expression of both nNOS and iNOS increase following induction of chronic arthritis, which in turn would presumably lead to an increase in the production of NO. This process could be involved in mediation of the secondary thermal hyperalgesia induced by chronic arthritis.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 119 (1998), S. 166-170 
    ISSN: 1432-1106
    Keywords: Key words Locus coeruleus ; Analgesia ; Inflammation ; Naloxone ; Rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  We evaluated the effects of systemic administration of a low dose of naloxone in rats with bilateral lesions in the area of the locus coeruleus (LC) under conditions of unilateral inflammation, compared with those in sham-operated rats. In each group, rats received a single s.c. injection of carrageenan (6 mg in 0.15 ml saline), and effects of a low dose of naloxone (5 μg/kg, i.p.) on thermal nociception were examined at 4 h and 7 days following the induction of unilateral hindpaw inflammation. The antinociceptive effect was assessed by prolongation of the paw withdrawal latency (PWL) to noxious thermal stimuli. Prior to induction of inflammation, the low dose of naloxone had no significant effect on PWLs in either the sham-operated or the LC-lesioned rats. Four hours after carrageenan injection, the low dose of naloxone produced prolongation of PWLs in the sham-operated rats but failed to induce antinociception in the LC-lesioned rats. Antinociceptive effects were observed in both groups of rats 7 days after carrageenan injection. These results suggest that the LC is involved in naloxone-induced antinociception during the early phase of inflammation.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 17 (1973), S. 177-189 
    ISSN: 1432-1106
    Keywords: Spinal cord ; Dorsal horn ; Cutaneous afferents ; Receptive fields ; Spino-cervical tract
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The locations of the cell bodies of origin of a pathway ascending in the dorsal part of the lateral funiculus of the cat spinal cord were mapped. It is presumed that the pathway is the spino-cervical tract. The locations of the neurons were determined by recording the antidromic action potentials in the lumbosacral enlargement evoked by stimulation of their axons at the third cervical segment, and then histologically reconstructing the recording sites. The cells were found to be scattered throughout laminae 4–6 of the dorsal horn, although most were in laminae 4 and 5. The conduction velocities of the axons ranged from 7 to 90 m/sec (mean 44 m/sec). A somatotopic relationship was observed between the locations of the cells within the dorsal horn and the distributions of their peripheral receptive fields. This somatotopic organization was oriented with respect to rostrocaudal and dorso-ventral axes as determined for the adult hindlimb by reference to its fetal development. The axes become distorted during development, but are still recognizable in the adult. Cells receiving afferent input from skin derived from rostral portions of the limb, including the medial surface of the adult foot, are located rostrally in the cord. The caudal limb, which includes the lateral surface of the foot in the adult, is represented caudally in the spinal cord. The dorsal limb or extensor surface projects to the lateral part of the dorsal horn, while the ventral limb or flexor surface is represented medially.
    Type of Medium: Electronic Resource
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