Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors

Nicotinic acetylcholine (nACh) receptors are known to be targets for modulation by a number of substances, including the opiates. It is known that acetylcholine (ACh) coexists with opioid peptides in cochlear efferent neurons, and such a colocalization has been proposed for the vestibular system. In...

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Autores principales: Lioudyno, M.I., Verbitsky, M., Holt, J.C., Elgoyhen, A.B., Guth, P.S.
Formato: JOUR
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03785955_v149_n1-2_p167_Lioudyno
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spelling todo:paper_03785955_v149_n1-2_p167_Lioudyno2023-10-03T15:33:09Z Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors Lioudyno, M.I. Verbitsky, M. Holt, J.C. Elgoyhen, A.B. Guth, P.S. Efferent Hair cell Interaction Morphine nACh receptor Vestibular system morphine nicotinic receptor opiate receptor acetylcholine Chrna9 protein, mouse morphine naloxone narcotic agent narcotic antagonist nicotinic receptor animal cell animal experiment article controlled study efferent nerve frog hair cell nonhuman patch clamp priority journal receptor blocking vestibular nervous system Xenopus laevis animal drug effect electric conductivity hair cell metabolism oocyte physiology Acetylcholine Animals Electric Conductivity Hair Cells Morphine Naloxone Narcotic Antagonists Narcotics Oocytes Rana pipiens Receptors, Nicotinic Xenopus laevis Nicotinic acetylcholine (nACh) receptors are known to be targets for modulation by a number of substances, including the opiates. It is known that acetylcholine (ACh) coexists with opioid peptides in cochlear efferent neurons, and such a colocalization has been proposed for the vestibular system. In the present study we test the hypothesis that morphine, an opioid receptor agonist with a broad spectrum of selectivity, modulates α9nACh receptor-mediated responses in frog vestibular hair cells. Morphine dose-dependently and reversibly inhibited ACh-induced currents as recorded by the perforated patch-clamp method. In the presence of morphine the ACh dose-response curve was shifted to the right in a parallel fashion, suggesting a competitive interaction. However, naloxone did not antagonize the inhibition produced by morphine. To test the hypothesis that morphine could interact with the α9nACh receptor without the involvement of opioid receptors, experiments were performed using Xenopus laevis oocytes injected with the α9nACh receptor cRNA. The currents activated by ACh in Xenopus oocytes, a system that lacks opioid receptors, were also dose-dependently inhibited by morphine. We conclude that morphine inhibits the α9nACh receptor-mediated response in hair cells and Xenopus oocytes through a mechanism which does not involve opioid receptors but may be a direct block of the α9nACh receptor. Copyright (C) 2000 Elsevier Science B.V. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03785955_v149_n1-2_p167_Lioudyno
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Efferent
Hair cell
Interaction
Morphine
nACh receptor
Vestibular system
morphine
nicotinic receptor
opiate receptor
acetylcholine
Chrna9 protein, mouse
morphine
naloxone
narcotic agent
narcotic antagonist
nicotinic receptor
animal cell
animal experiment
article
controlled study
efferent nerve
frog
hair cell
nonhuman
patch clamp
priority journal
receptor blocking
vestibular nervous system
Xenopus laevis
animal
drug effect
electric conductivity
hair cell
metabolism
oocyte
physiology
Acetylcholine
Animals
Electric Conductivity
Hair Cells
Morphine
Naloxone
Narcotic Antagonists
Narcotics
Oocytes
Rana pipiens
Receptors, Nicotinic
Xenopus laevis
spellingShingle Efferent
Hair cell
Interaction
Morphine
nACh receptor
Vestibular system
morphine
nicotinic receptor
opiate receptor
acetylcholine
Chrna9 protein, mouse
morphine
naloxone
narcotic agent
narcotic antagonist
nicotinic receptor
animal cell
animal experiment
article
controlled study
efferent nerve
frog
hair cell
nonhuman
patch clamp
priority journal
receptor blocking
vestibular nervous system
Xenopus laevis
animal
drug effect
electric conductivity
hair cell
metabolism
oocyte
physiology
Acetylcholine
Animals
Electric Conductivity
Hair Cells
Morphine
Naloxone
Narcotic Antagonists
Narcotics
Oocytes
Rana pipiens
Receptors, Nicotinic
Xenopus laevis
Lioudyno, M.I.
Verbitsky, M.
Holt, J.C.
Elgoyhen, A.B.
Guth, P.S.
Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors
topic_facet Efferent
Hair cell
Interaction
Morphine
nACh receptor
Vestibular system
morphine
nicotinic receptor
opiate receptor
acetylcholine
Chrna9 protein, mouse
morphine
naloxone
narcotic agent
narcotic antagonist
nicotinic receptor
animal cell
animal experiment
article
controlled study
efferent nerve
frog
hair cell
nonhuman
patch clamp
priority journal
receptor blocking
vestibular nervous system
Xenopus laevis
animal
drug effect
electric conductivity
hair cell
metabolism
oocyte
physiology
Acetylcholine
Animals
Electric Conductivity
Hair Cells
Morphine
Naloxone
Narcotic Antagonists
Narcotics
Oocytes
Rana pipiens
Receptors, Nicotinic
Xenopus laevis
description Nicotinic acetylcholine (nACh) receptors are known to be targets for modulation by a number of substances, including the opiates. It is known that acetylcholine (ACh) coexists with opioid peptides in cochlear efferent neurons, and such a colocalization has been proposed for the vestibular system. In the present study we test the hypothesis that morphine, an opioid receptor agonist with a broad spectrum of selectivity, modulates α9nACh receptor-mediated responses in frog vestibular hair cells. Morphine dose-dependently and reversibly inhibited ACh-induced currents as recorded by the perforated patch-clamp method. In the presence of morphine the ACh dose-response curve was shifted to the right in a parallel fashion, suggesting a competitive interaction. However, naloxone did not antagonize the inhibition produced by morphine. To test the hypothesis that morphine could interact with the α9nACh receptor without the involvement of opioid receptors, experiments were performed using Xenopus laevis oocytes injected with the α9nACh receptor cRNA. The currents activated by ACh in Xenopus oocytes, a system that lacks opioid receptors, were also dose-dependently inhibited by morphine. We conclude that morphine inhibits the α9nACh receptor-mediated response in hair cells and Xenopus oocytes through a mechanism which does not involve opioid receptors but may be a direct block of the α9nACh receptor. Copyright (C) 2000 Elsevier Science B.V.
format JOUR
author Lioudyno, M.I.
Verbitsky, M.
Holt, J.C.
Elgoyhen, A.B.
Guth, P.S.
author_facet Lioudyno, M.I.
Verbitsky, M.
Holt, J.C.
Elgoyhen, A.B.
Guth, P.S.
author_sort Lioudyno, M.I.
title Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors
title_short Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors
title_full Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors
title_fullStr Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors
title_full_unstemmed Morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors
title_sort morphine inhibits an α9-acetylcholine nicotinic receptor-mediated response by a mechanism which does not involve opioid receptors
url http://hdl.handle.net/20.500.12110/paper_03785955_v149_n1-2_p167_Lioudyno
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AT verbitskym morphineinhibitsana9acetylcholinenicotinicreceptormediatedresponsebyamechanismwhichdoesnotinvolveopioidreceptors
AT holtjc morphineinhibitsana9acetylcholinenicotinicreceptormediatedresponsebyamechanismwhichdoesnotinvolveopioidreceptors
AT elgoyhenab morphineinhibitsana9acetylcholinenicotinicreceptormediatedresponsebyamechanismwhichdoesnotinvolveopioidreceptors
AT guthps morphineinhibitsana9acetylcholinenicotinicreceptormediatedresponsebyamechanismwhichdoesnotinvolveopioidreceptors
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