Involvement of μ-opioid receptors in potentiation of apomorphine-induced climbing behavior by morphine: studies using μ-opioid receptor gene knockout mice

2000 ◽  
Vol 78 (1-2) ◽  
pp. 204-206 ◽  
Author(s):  
Choon-Gon Jang ◽  
Younjoo Park ◽  
Sachiko Tanaka ◽  
Tangeng Ma ◽  
Horace H Loh ◽  
...  
2002 ◽  
Vol 945 (1) ◽  
pp. 9-19 ◽  
Author(s):  
Robin J Goody ◽  
Sarah M Oakley ◽  
Dominique Filliol ◽  
Brigitte L Kieffer ◽  
Ian Kitchen

1997 ◽  
Vol 778 (1) ◽  
pp. 73-88 ◽  
Author(s):  
Ian Kitchen ◽  
Susan J Slowe ◽  
Hans W.D Matthes ◽  
Brigitte Kieffer

2020 ◽  
Vol 20 (31) ◽  
pp. 2866-2877
Author(s):  
Hirokazu Mizoguchi ◽  
Hideaki Fujii

Since a μ-opioid receptor gene containing multiple exons has been identified, the variety of splice variants for μ-opioid receptors have been reported in various species. Amidino-TAPA and IBNtxA have been discovered as new analgesics with different pharmacological profiles from morphine. These new analgesics show a very potent analgesic effect but do not have dependence liability. Interestingly, these analgesics show the selectivity to the morphine-insensitive μ-opioid receptor splice variants. The splice variants, sensitive to these new analgesics but insensitive to morphine, may be a better molecular target to develop the analgesics without side effects.


2006 ◽  
Vol 51 (3) ◽  
pp. 612-622 ◽  
Author(s):  
Jalal Izadi Mobarakeh ◽  
Kazuhiro Takahashi ◽  
Shinobu Sakurada ◽  
Atsuo Kuramasu ◽  
Kazuhiko Yanai

Pain ◽  
2005 ◽  
Vol 118 (1) ◽  
pp. 254-262 ◽  
Author(s):  
Jalal Izadi Mobarakeh ◽  
Kazuhiro Takahashi ◽  
Shinobu Sakurada ◽  
Seiji Nishino ◽  
Hiroyuki Watanabe ◽  
...  

Peptides ◽  
2007 ◽  
Vol 28 (6) ◽  
pp. 1229-1239 ◽  
Author(s):  
Elaine C. Gavioli ◽  
Anna Rizzi ◽  
Giuliano Marzola ◽  
Silvia Zucchini ◽  
Domenico Regoli ◽  
...  

2012 ◽  
Vol 107 (3) ◽  
pp. 1022-1031 ◽  
Author(s):  
Melissa A. Herman ◽  
Richard A. Gillis ◽  
Stefano Vicini ◽  
Kenneth L. Dretchen ◽  
Niaz Sahibzada

Our laboratory previously reported that gastric activity is controlled by a robust GABAA receptor-mediated inhibition in the medial nucleus of the tractus solitarius (mNTS) ( Herman et al. 2009 ), and that μ-opioid receptor activation inhibits gastric tone by suppression of this GABA signaling ( Herman et al. 2010 ). These data raised two questions: 1) whether any of this inhibition was due to tonic GABAA receptor-mediated conductance in the mNTS; and 2) whether μ-opioid receptor activation suppressed both tonic and phasic GABA signaling. In whole cell recordings from rat mNTS neurons, application of three GABAA receptor antagonists (gabazine, bicuculline, and picrotoxin) produced a persistent reduction in holding current and decrease in population variance or root mean square (RMS) noise, suggesting a blockade of tonic GABA signaling. Application of gabazine at a lower concentration abolished phasic currents, but had no effect on tonic currents or RMS noise. Application of the δ-subunit preferring agonist gaboxadol (THIP) produced a dose-dependent persistent increase in holding current and RMS noise. Pretreatment with tetrodotoxin prevented the action of gabazine, but had no effect on the THIP-induced current. Membrane excitability was unaffected by the selective blockade of phasic inhibition, but was increased by blockade of both phasic and tonic currents. In contrast, activation of tonic currents decreased membrane excitability. Application of the μ-opioid receptor agonist DAMGO produced a persistent reduction in holding current that was not observed following pretreatment with a GABAA receptor antagonist and was not evident in mice lacking the δ-subunit. These data suggest that mNTS neurons possess a robust tonic inhibition that is mediated by GABAA receptors containing the δ-subunit, that determines membrane excitability, and that is partially regulated by μ-opioid receptors.


2001 ◽  
Vol 94 (1-2) ◽  
pp. 197-199 ◽  
Author(s):  
Choon-Gon Jang ◽  
Seok-Yong Lee ◽  
Younjoo Park ◽  
Tangeng Ma ◽  
Horace H Loh ◽  
...  

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