Magnetic field exposure was consistently found to affect pain inhibition (i.e. analgesia). Recently, we showed that an extreme reduction of the ambient magnetic and electric environment, by mu-metal shielding, also affected stress-induced analgesia (SIA) in C57 mice. Using CD1 mice, we report here the same findings from replication studies performed independently in Pisa, Italy and London, ON, Canada. Also, neither selective vector nulling of the static component of the ambient magnetic field with Helmholtz coils, nor copper shielding of only the ambient electric field, affected SIA in mice. We further show that a pre-stress exposure to the mu-metal box is necessary for the anti-analgesic effects to occur. The differential effects of the two near-zero magnetic conditions may depend on the elimination (obtained only by mu-metal shielding) of the extremely weak time-varying component of the magnetic environment. This would provide the first direct and repeatable evidence for a behavioural and physiological effect of very weak time-varying magnetic fields, suggesting the existence of a very sensitive magnetic discrimination in the endogenous mechanisms that underlie SIA. This has important implications for other reported effects of exposures to very weak magnetic fields and for the theoretical work that considers the mechanisms underlying the biological detection of weak magnetic fields.

Shielding, but not zeroing of the ambient magnetic field reduces stress-induced analgesia in mice

Del Seppia C;Ghione S;
2002

Abstract

Magnetic field exposure was consistently found to affect pain inhibition (i.e. analgesia). Recently, we showed that an extreme reduction of the ambient magnetic and electric environment, by mu-metal shielding, also affected stress-induced analgesia (SIA) in C57 mice. Using CD1 mice, we report here the same findings from replication studies performed independently in Pisa, Italy and London, ON, Canada. Also, neither selective vector nulling of the static component of the ambient magnetic field with Helmholtz coils, nor copper shielding of only the ambient electric field, affected SIA in mice. We further show that a pre-stress exposure to the mu-metal box is necessary for the anti-analgesic effects to occur. The differential effects of the two near-zero magnetic conditions may depend on the elimination (obtained only by mu-metal shielding) of the extremely weak time-varying component of the magnetic environment. This would provide the first direct and repeatable evidence for a behavioural and physiological effect of very weak time-varying magnetic fields, suggesting the existence of a very sensitive magnetic discrimination in the endogenous mechanisms that underlie SIA. This has important implications for other reported effects of exposures to very weak magnetic fields and for the theoretical work that considers the mechanisms underlying the biological detection of weak magnetic fields.
2002
Istituto di Fisiologia Clinica - IFC
269
193
201
Nocicezione
Dolore
Soglia dolorifica
Elettromagnetismo
I risultati di questo studio, ottenuti in parte in Italia e in parte in Canada confermano una nostra precedente ricerca (Del Seppia et al. 2000) dimostrando, cosa non sempre facile in questi studi, la replicabilità dei risultati. Inoltre è stata osservata per la prima volta che la nocicezione viene alterata a secondo del modo con cui il campo geomagnetico viene ridotto. Infatti la permanenza in un campo ipogeomagnetico schermato modifica l’ipoalgesia da stress, lo stesso effetto non si osserva con un campo annullato. La spiegazione sembra essere che per ottenere delle modifiche sulla nocicezione sia importante la riduzione sia del campo statico che di quelli variabili nel tempo. Infatti, mentre il contenitore di mu-metal scherma sia i campi statici (campo geomagnetico) che i campi dinamici (ad es. quelli generati dalle apparecchiature presenti nei laboratori), le bobine di Helmholtz hanno la caratteristica di schermare soltanto i campi statici. Impact factor 2002 (3.396)
1
info:eu-repo/semantics/article
262
Choleris E ; Del Seppia C ; Thomas AW; Luschi P; Ghione S; Moran GR; Prato FS.
01 Contributo su Rivista::01.01 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/45024
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