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Enregistrement W3119640941 · doi:10.1097/aln.0000000000003665

Perioperative Use of Gabapentinoids: Comment

2021· letter· en· W3119640941 sur OpenAlexaff
Po‐Yi Paul Su, Zhonghui Guan

Notice bibliographique

RevueAnesthesiology · 2021
Typeletter
Langueen
DomaineMedicine
ThématiquePain Mechanisms and Treatments
Établissements canadiensUniversité Laval
Organismes subventionnairesNational Institute of Neurological Disorders and Stroke
Mots-clésGabapentinNeuropathic painPregabalinMedicineDorsal root ganglionNerve injuryAnesthesiaNMDA receptorAnalgesicSpinal cordPharmacologyNeuroscienceReceptorInternal medicinePathologyPsychiatryPsychology

Résumé

récupéré en direct d'OpenAlex

Gabapentinoids, including gabapentin and pregabalin, bind to the α2δ1 subunit of calcium channel (α2δ1) to relieve neuropathic pain.1 Although gabapentinoids are among the most effective medications to treat chronic neuropathic pain,2 their use in managing postoperative acute pain has been controversial. A recent meta-analysis of 281 randomized controlled trials by Verret et al. shows that gabapentinoids do not provide clinically significant analgesic effect for postoperative acute pain.3 It would be of great interest to discuss the potential mechanism behind why gabapentinoids have limited effect in postoperative acute pain.α2δ1 is constitutively expressed in dorsal root ganglion. Its expression is greatly induced after nerve injury,4 and the upregulated α2δ1 is transported from dorsal root ganglion sensory neurons to spinal cord.5 Because α2δ1 is a subunit of the voltage-activated Ca2+ channel complex, it has been postulated that gabapentinoids work through modulating Ca2+ channels. However, gabapentinoids do not alter the activity of Ca2+ channels, suggesting that the effect of gabapentinoids in treating pain is independent from the regulation of Ca2+ channel activity.6,7Chen et al. recently discovered a novel mechanism through which gabapentinoids relieve neuropathic pain.7 They found that α2δ1 binds to N-methyl-d-aspartate (NMDA) receptor in both rodent and human to enhance its activity in spinal cord after nerve injury, and gabapentin prevents α2δ1-mediated NMDA receptor hyperactivity.7 Importantly, baseline α2δ1 does not facilitate spinal cord NMDA receptor activity, but the upregulated α2δ1, like after nerve injury, is associated with the enhanced spinal cord NMDA receptor activity and neuropathic pain behavior.7 Notably, α2δ1 does not contribute to the acute pain immediately after nerve injury. In preclinical models, it takes up to 2 days for α2δ1 to be fully upregulated after nerve injury,4 and knocking down α2δ1 has no effect on neuropathic pain behavior within the first 2 days after nerve injury, even though it attenuates pain behavior at later time points.7 Taken together, Chen et al. have revealed a new mechanism in which gabapentinoids reduce neuropathic pain by inhibiting spinal cord NMDA receptor hyperactivity mediated by upregulated α2δ1.The role of the NMDA receptor in many pain conditions, including postoperative pain, has been well recognized.8 The interaction between α2δ1 and the NMDA receptor explains why gabapentinoids are effective in treating chronic neuropathic pain, but not postoperative acute pain. In chronic neuropathic pain, α2δ1 is upregulated to enhance NMDA receptor activity in spinal cord to produce neuropathic pain, and gabapentinoids prevent the interaction between the upregulated α2δ1 and NMDA receptor to relieve neuropathic pain. In healthy uninjured state, the interaction between baseline α2δ1 and the NMDA receptor is minimal, and gabapentinoids have no influence on baseline NMDA receptor activity in spinal cord. It takes time for α2δ1 to be fully induced after injury, so during the perioperative period it is likely that α2δ1 remains at or near baseline level with minimal interaction with the NMDA receptor. As a result, perioperative gabapentinoids, especially administered before surgical injury, have limited effects on spinal cord NMDA receptor activity to reduce acute pain immediately after surgery. Furthermore, as gabapentin treatment does not prevent α2δ1 upregulation after nerve injury,5 it is also unlikely that perioperative gabapentinoids can prevent chronic postoperative pain, consistent with meta-analysis from Verret et al.3In conclusion, gabapentinoids disrupt the interaction between the upregulated α2δ1 and NMDA receptor to inhibit spinal cord NMDA receptor hyperactivity in treating chronic neuropathic pain. As the acute postoperative pain precedes injury-induced α2δ1 upregulation, and gabapentinoids have no effect on the NMDA receptor without α2δ1 upregulation, perioperative gabapentinoids do not have clinically significant impact on postoperative pain.Dr. Guan is supported by grant No. R01 NS100801 from the National Institutes of Health (Bethesda, Maryland).The authors declare no competing interests.

Récupéré en direct depuis OpenAlex et désinversé. Les résumés ne sont pas conservés dans cette base de données : les index inversés représentent 8,6 Go des 9,3 Go de texte de la base, et le serveur dispose de 13 Go libres.

Comment cette classification a été obtenuedéplier

Prédiction machine sur la base complète

Imitation des enseignants

Ni prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.

score de la tête « metaresearch » (Codex)0,005
score de la tête « metaresearch » (Gemma)0,031
Version: metacan-v3-hybrid-931329e0061cStatut de validation: machine_predicted_unvalidated
Catégories candidatesaucune
Catégories consensuellesaucune
DomaineSignal candidat: aucune · Signal consensuel: aucune
Devis d'étudeSignal candidat: Sans objet · Signal consensuel: Sans objet
GenreSignal candidat: Commentaire · Signal consensuel: Commentaire
Score de désaccord entre enseignants0,008
Score d'incertitude au seuil0,027

Scores du classifieur distillé par catégorie (deux têtes)

CatégorieCodexGemma
Métarecherche0,0050,031
Méta-épidémiologie (sens strict)0,0010,000
Méta-épidémiologie (sens large)0,0010,002
Bibliométrie0,0010,001
Études des sciences et des technologies0,0010,002
Communication savante0,0010,003
Science ouverte0,0020,001
Intégrité de la recherche0,0080,013
Charge utile insuffisante (le modèle a refusé de juger)0,0080,005

Scores machine (provisoires)

Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.

Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.

Tête enseignante Opus0,063
Tête enseignante GPT0,281
Écart entre enseignants0,218 · la distance entre les deux têtes enseignantes sur ce seul travail
Statut de validationscore_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découle

Classification

machine, non validée

Prédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.

Les modèles n’ont appliqué aucune catégorie : rien dans la taxonomie ne correspondait à ce travail.
Devis d'étudeSans objet
Domainenon disponible
GenreCommentaire

Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».

En bref

Citations2
Publié2021
Routes d'admission1
Résumé présentoui

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