THE DIFFERENTIAL CONTRIBUTION OF CAPSAICIN-SENSITIVE AFFERENTS TO BEHAVIORAL AND CARDIOVASCULAR MEASURES OF BRIEF AND PERSISTENT NOCICEPTION AND TO FOS EXPRESSION IN THE FORMALIN TEST
Ma. Peterson et al., THE DIFFERENTIAL CONTRIBUTION OF CAPSAICIN-SENSITIVE AFFERENTS TO BEHAVIORAL AND CARDIOVASCULAR MEASURES OF BRIEF AND PERSISTENT NOCICEPTION AND TO FOS EXPRESSION IN THE FORMALIN TEST, Brain research, 755(1), 1997, pp. 9-16
Intraplantar injection of dilute formalin evokes brief (Phase 1) and p
ersistent (Phase 2) increases in primary afferent activity, pain behav
ior, and cardiovascular responses, and induces spinal cord Fos-like im
munoreactivity (Fos-LI). Although previous studies demonstrated that t
he destruction of small diameter primary afferents with neonatal capsa
icin treatment decrease formalin-evoked nociception, these studies onl
y evaluated behavioral responses, and did not distinguish between Phas
e 1 and 2. To address these questions, we simultaneously evaluated for
malin-evoked pain behavior (flinching of the afflicted paw), cardiovas
cular responses (heart rate and mean arterial pressure), and lumbar sp
inal cord Fos expression in control rats and in rats treated with caps
aicin (100 mg/kg) one day postpartum. We found that neonatal capsaicin
-treated rats, compared to controls, exhibited similar cardiovascular
responses and slightly less flinching behavior during Phase 1. During
Phase 2, however, capsaicin treated rats exhibited 59% less flinching
and 45% smaller heart rate responses. Also, in capsaicin-treated rats,
we counted 59% fewer Fos-labeled neurons in the spinal cord. These re
sults indicate that capsaicin-sensitive afferents contribute to formal
in-evoked behavioral and cardiovascular responses and to spinal cord n
euronal responses. The differential effect of neonatal capsaicin on no
ciception during Phase 1 and Phase 2 suggests that sensitization mecha
nisms during Phase 1 do not contribute to the magnitude of nociceptive
responses during Phase 2.