Involvement of estrogen in rapid pain modulation in the rat spinal cord.
Identifieur interne : 002243 ( Main/Exploration ); précédent : 002242; suivant : 002244Involvement of estrogen in rapid pain modulation in the rat spinal cord.
Auteurs : Yan Zhang [République populaire de Chine] ; Ning Lü ; Zhi-Qi Zhao ; Yu-Qiu ZhangSource :
- Neurochemical research [ 1573-6903 ] ; 2012.
Descripteurs français
- KwdFr :
- Animaux, Douleur (physiopathologie), Femelle, Moelle spinale (métabolisme), Moelle spinale (physiopathologie), Mâle, Oestrogènes (physiologie), Rat Sprague-Dawley, Rats, Réaction de polymérisation en chaine en temps réel, Récepteurs des oestrogènes (métabolisme), Technique de Western, Techniques de patch-clamp.
- MESH :
- métabolisme : Moelle spinale, Récepteurs des oestrogènes.
- physiologie : Oestrogènes.
- physiopathologie : Douleur, Moelle spinale.
- Animaux, Femelle, Mâle, Rat Sprague-Dawley, Rats, Réaction de polymérisation en chaine en temps réel, Technique de Western, Techniques de patch-clamp.
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Receptors, Estrogen.
- chemical , physiology : Estrogens.
- metabolism : Spinal Cord.
- physiopathology : Pain, Spinal Cord.
- Animals, Blotting, Western, Female, Male, Patch-Clamp Techniques, Rats, Rats, Sprague-Dawley, Real-Time Polymerase Chain Reaction.
Abstract
The pivotal role of estrogens in the pain sensitivity has been investigated in many ways. Traditionally, it is ascribed to the slow genomic changes mediated by classical nuclear estrogen receptors (ER), ERα and ERβ, depending on peripheral estrogens. Recently, it has become clear that estrogens can also signal through membrane ERs (mERs), such as G-protein-coupled ER1 (GPER1), mediating the non-genomic effects. However, the spinal specific role played by ERs and the underlying cellular mechanisms remain elusive. The present study investigated the rapid estrogenic regulation of nociception at the spinal level. Spinal administration of 17β-estradiol (E2), the most potent natural estrogen, acutely produced a remarkable mechanical allodynia and thermal hyperalgesia without significant differences among male, female and ovariectomized (Ovx) rats. E2-induced the pro-nociceptive effects were partially abrogated by ICI 182,780 (ERs antagonist), and mimicked by E2-BSA (a mER agonist). Inhibition of local E2 synthesis by 1,4,6-Androstatrien-3,17-dione (ATD, a potent irreversible aromatase inhibitor), or blockade of ERs by ICI 182,780 produced an inhibitory effect on the late phase of formalin nociceptive responses. Notably, lumbar puncture injection of G15 (a selective GPER1 antagonist) resulted in similar but more efficient inhibition of formalin nociceptive responses as compared with ICI 182,780. At the cellular level, the amplitude and decay time of spontaneous inhibitory postsynaptic currents were attenuated by short E2 or E2-BSA treatment in spinal slices. These results indicate that estrogen acutely facilitates nociceptive transmission in the spinal cord via activation of membrane-bound estrogen receptors.
DOI: 10.1007/s11064-012-0859-1
PubMed: 22903468
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">The pivotal role of estrogens in the pain sensitivity has been investigated in many ways. Traditionally, it is ascribed to the slow genomic changes mediated by classical nuclear estrogen receptors (ER), ERα and ERβ, depending on peripheral estrogens. Recently, it has become clear that estrogens can also signal through membrane ERs (mERs), such as G-protein-coupled ER1 (GPER1), mediating the non-genomic effects. However, the spinal specific role played by ERs and the underlying cellular mechanisms remain elusive. The present study investigated the rapid estrogenic regulation of nociception at the spinal level. Spinal administration of 17β-estradiol (E2), the most potent natural estrogen, acutely produced a remarkable mechanical allodynia and thermal hyperalgesia without significant differences among male, female and ovariectomized (Ovx) rats. E2-induced the pro-nociceptive effects were partially abrogated by ICI 182,780 (ERs antagonist), and mimicked by E2-BSA (a mER agonist). Inhibition of local E2 synthesis by 1,4,6-Androstatrien-3,17-dione (ATD, a potent irreversible aromatase inhibitor), or blockade of ERs by ICI 182,780 produced an inhibitory effect on the late phase of formalin nociceptive responses. Notably, lumbar puncture injection of G15 (a selective GPER1 antagonist) resulted in similar but more efficient inhibition of formalin nociceptive responses as compared with ICI 182,780. At the cellular level, the amplitude and decay time of spontaneous inhibitory postsynaptic currents were attenuated by short E2 or E2-BSA treatment in spinal slices. These results indicate that estrogen acutely facilitates nociceptive transmission in the spinal cord via activation of membrane-bound estrogen receptors.</div>
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