Menthol, after topical application, causes a feeling of coolness due to stimulation of 'cold' receptors by inhibiting Ca++ currents of neuronal membranes. Since Ca++ channel blockers are endowed with analgesic properties, the aim of the present study was to investigate the potential antinociceptive effect of menthol. (-)-Menthol produced a dose-dependent increase in the pain threshold in the mouse hot-plate (3-10 mg kg(-1) p.o.) and abdominal constriction (3-10 mg kg(-1) p.o.; 10 mug per mouse intracerebroventricularly (i.c.v.))tests. The antinociceptive effect of H-menthol was antagonised by the unselective opioid antagonist naloxone and by the selective K-antagonist nor-NBI. Conversely, CTOP ( L-antagonist), 7-benzylidenenal-trexone (delta(1) antagonist) and naltriben (delta(2) antagonist) did not prevent (-)-menthol antinociception. In both tests, (+)-menthol (10-50 mg kg(-1) p.o.; 10-30 mug per mouse i.c.v.) was unable to modify the pain threshold. These results indicate that (-)-menthol is endowed with analgesic properties mediated through a selective activation Of kappa-opioid receptors. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
Menthol: a natural analgesic compound / Nicoletta, Galeotti; Lorenzo Di Cesare, Mannelli; Mazzanti, Gabriela; Alessandro, Bartolini; Carla, Ghelardini. - In: NEUROSCIENCE LETTERS. - ISSN 0304-3940. - STAMPA. - 322:3(2002), pp. 145-148. [10.1016/s0304-3940(01)02527-7]
Menthol: a natural analgesic compound
MAZZANTI, Gabriela;
2002
Abstract
Menthol, after topical application, causes a feeling of coolness due to stimulation of 'cold' receptors by inhibiting Ca++ currents of neuronal membranes. Since Ca++ channel blockers are endowed with analgesic properties, the aim of the present study was to investigate the potential antinociceptive effect of menthol. (-)-Menthol produced a dose-dependent increase in the pain threshold in the mouse hot-plate (3-10 mg kg(-1) p.o.) and abdominal constriction (3-10 mg kg(-1) p.o.; 10 mug per mouse intracerebroventricularly (i.c.v.))tests. The antinociceptive effect of H-menthol was antagonised by the unselective opioid antagonist naloxone and by the selective K-antagonist nor-NBI. Conversely, CTOP ( L-antagonist), 7-benzylidenenal-trexone (delta(1) antagonist) and naltriben (delta(2) antagonist) did not prevent (-)-menthol antinociception. In both tests, (+)-menthol (10-50 mg kg(-1) p.o.; 10-30 mug per mouse i.c.v.) was unable to modify the pain threshold. These results indicate that (-)-menthol is endowed with analgesic properties mediated through a selective activation Of kappa-opioid receptors. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
