M. Sudo et al., Thiopental directly depresses lumbar dorsal horn neuronal responses to noxious mechanical stimulation in goats, ACT ANAE SC, 45(7), 2001, pp. 823-829
Citations number
19
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Background: Thiopental has hypnotic actions in the brain, but it also depre
sses nociceptive transmission. in this study we examined whether thiopental
had direct (spinal) and/or indirect (supraspinal) effects on the responses
of single lumbar dorsal horn neurons to noxious mechanical stimulation, us
ing a method to deliver thiopental differentially to either the torso or cr
anial circulation in goats.
Methods: Goats (n=10) were anesthetized with isoflurane and neck dissection
s performed to permit cranial bypass. A lumbar laminectomy was made to perm
it single-unit recording of lumbar dorsal horn neuronal activity (1-2 neuro
ns/animal). Isoflurane was maintained at 0.8 +/-0.1% to both head and torso
throughout the study. During cranial bypass, thiopental was separately adm
inistered to the torso (low dose, 1.5 +/-0.5 mg/kg; high dose, 3.7 +/-0.5 m
g/kg) or cranial (low dose, 0.12 +/-0.03 mg/kg; high dose, 0.2 mg/kg) circu
lation.
Results: Thiopental administered to the torso significantly depressed dorsa
l horn neuronal responses to noxious stimulation at the high dose: 757 +/-
471 to 392 +/- 303 impulses/min at I min post-injection, P <0.006 (n=14); e
voked responses recovered at 5 min post-injection. At the low dose, there w
as a similar numerical decrease, but this did not reach significance: 876 /- 780 to 407 +/- 499 impulses/min at I min post-injection, P >0.05 (n=6).
No significant change was observed when thiopental was administered to the
cranial circulation: low dose, 1061 +/- 1167 to 965 +/- 874 impulses/min at
1 min post-injection, P >0.05 (n=10); high dose, 864 +/- 331 to 917 +/- 52
5 impulses/min at 1 min postinjection, P >0.05 (n=8).
Conclusion: Thiopental has a direct (spinal) depressant effect on dorsal ne
uronal responses to noxious stimulus, but no significant supraspinal effect
.