2014, Number 5
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Rev Med Inst Mex Seguro Soc 2014; 52 (5)
Beta-1 adrenoceptor blockade decreases the fi ring rate to painful stimuli in spinal widedynamic range neurons in rats
Lamothe-Molina PJ, Lamothe-Molina PA, López-Ávila A
Language: Spanish
References: 32
Page: 494-501
PDF size: 337.33 Kb.
ABSTRACT
Background: It is known that epinephrine/norepinephrine
inhibit acute pain transmission. However, the role
of β-adrenoceptors is not clear. Thus, we analyzed if
β-1 and/or β-2 adrenoceptors can modulate acute pain
transmission by performing
in vivo single unit recordings
during painful and non-painful peripheral stimulation
in rats.
Methods: Longitudinal study in which we analyzed
seven groups of male rats Wistar: control group
(
n = 11): saline (0.9 %); EPI group (
n = 8): epinephrine
100 mcg; AGOβ1 group (
n = 8): dobutamine 125 mcg;
ANTβ1 group (
n = 9): metoprolol 100 mcg; AGOβ2
group (
n = 7): clenbuterol 100 mcg; ANTβ2 group
(
n = 8): butoxamine 100 mcg; ANTβ1 + EPI group
(
n = 10): metoprolol 100 mcg + epinephrine 100 mcg.
For the statistical analysis we used ANOVA.
Results: Epinephrine significantly reduced the
basalfirin grate (BFR) in 34.1 % (
p ‹ 0.05) and also
the evoked response by painful stimulation in 56 %
(
p ‹ 0.05). No change was observed in the evoked
response by non-painful stimulation. ANTβ1 was the
only β-adrenoceptor acting drug that significantly
reduced the evoked response by painful stimulation in
41 % (
p ‹ 0.05). None of the other drugs alone affected
either the BFR or the evoked response to non-painful
or painful stimulation.
Conclusion: It is the first time that a β1-adrenoceptor
antagonist (metoprolol) probes to be effective in reducing
the response to painful stimulation in WDR neurons.
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