Let-7 microRNAs and opioid tolerance

This chapter will focus on the role of microRNAs (miRs) in regulating the actions of opioid drugs through the opioid receptors. Opioids, such as morphine, are analgesics that are used for treating many forms of acute and chronic pain. However, their chronic use is limited by undesirable effects suc...

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Main Authors: YING eHE, ZAIJIE JIM eWANG
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-06-01
Series:Frontiers in Genetics
Subjects:
miR
Online Access:http://journal.frontiersin.org/Journal/10.3389/fgene.2012.00110/full
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spelling doaj-9c4bab79eade46bf9bee24f2b11b7fff2020-11-24T22:33:50ZengFrontiers Media S.A.Frontiers in Genetics1664-80212012-06-01310.3389/fgene.2012.0011025700Let-7 microRNAs and opioid toleranceYING eHE0ZAIJIE JIM eWANG1UNIVERSITY OF ILLINOIS AT CHICAGOUNIVERSITY OF ILLINOIS AT CHICAGOThis chapter will focus on the role of microRNAs (miRs) in regulating the actions of opioid drugs through the opioid receptors. Opioids, such as morphine, are analgesics that are used for treating many forms of acute and chronic pain. However, their chronic use is limited by undesirable effects such as opioid tolerance. The µ opioid receptor (MOR) is the primary receptor responsible for opioids’ analgesia and antinociceptive tolerance. The long 3’-untranslated region (3’-UTR) of MOR mRNA is of great interest since this region may contain elements for the post-transcriptional regulation of receptor expression, such as altering the stability of mRNA, influencing translational efficiency and controlling mRNA transport. Indeed, it was reported that human MOR expression was increased after a 712 bp sequence, immediately downstream of the stop codon, was removed. MicroRNAs are small noncoding RNA molecules that exert their functions through base-pairing with partially complementary sequences in the 3’-UTR of target mRNAs, resulting in decreased polypeptide formation from those mRNAs. Since the discovery of the first miR, lin-4 in C. elegans, hundreds of miRs have been identified from humans to viruses, which have provided a crucial and pervasive layer of post-transcriptional gene regulation. The nervous system is a rich source of miR expression, with a diversity of miR functions in fundamental neurobiological processes including neuronal development, plasticity, metabolism and apoptosis. Recently, the let-7 family of miRs is found to be a critical regulator of MOR function in opioid tolerance. Let-7 is the first identified human miR. Its family members are highly conserved across species in sequence and function. In the review, we will present a brief review of the opioid receptors, their regulation, and opioid tolerance as well as an overview of miRs and a perspective how miRs may interact with MOR and serve as a regulator of opioid tolerance.http://journal.frontiersin.org/Journal/10.3389/fgene.2012.00110/fullPainAddictionepigeneticsopioidmiR
collection DOAJ
language English
format Article
sources DOAJ
author YING eHE
ZAIJIE JIM eWANG
spellingShingle YING eHE
ZAIJIE JIM eWANG
Let-7 microRNAs and opioid tolerance
Frontiers in Genetics
Pain
Addiction
epigenetics
opioid
miR
author_facet YING eHE
ZAIJIE JIM eWANG
author_sort YING eHE
title Let-7 microRNAs and opioid tolerance
title_short Let-7 microRNAs and opioid tolerance
title_full Let-7 microRNAs and opioid tolerance
title_fullStr Let-7 microRNAs and opioid tolerance
title_full_unstemmed Let-7 microRNAs and opioid tolerance
title_sort let-7 micrornas and opioid tolerance
publisher Frontiers Media S.A.
series Frontiers in Genetics
issn 1664-8021
publishDate 2012-06-01
description This chapter will focus on the role of microRNAs (miRs) in regulating the actions of opioid drugs through the opioid receptors. Opioids, such as morphine, are analgesics that are used for treating many forms of acute and chronic pain. However, their chronic use is limited by undesirable effects such as opioid tolerance. The µ opioid receptor (MOR) is the primary receptor responsible for opioids’ analgesia and antinociceptive tolerance. The long 3’-untranslated region (3’-UTR) of MOR mRNA is of great interest since this region may contain elements for the post-transcriptional regulation of receptor expression, such as altering the stability of mRNA, influencing translational efficiency and controlling mRNA transport. Indeed, it was reported that human MOR expression was increased after a 712 bp sequence, immediately downstream of the stop codon, was removed. MicroRNAs are small noncoding RNA molecules that exert their functions through base-pairing with partially complementary sequences in the 3’-UTR of target mRNAs, resulting in decreased polypeptide formation from those mRNAs. Since the discovery of the first miR, lin-4 in C. elegans, hundreds of miRs have been identified from humans to viruses, which have provided a crucial and pervasive layer of post-transcriptional gene regulation. The nervous system is a rich source of miR expression, with a diversity of miR functions in fundamental neurobiological processes including neuronal development, plasticity, metabolism and apoptosis. Recently, the let-7 family of miRs is found to be a critical regulator of MOR function in opioid tolerance. Let-7 is the first identified human miR. Its family members are highly conserved across species in sequence and function. In the review, we will present a brief review of the opioid receptors, their regulation, and opioid tolerance as well as an overview of miRs and a perspective how miRs may interact with MOR and serve as a regulator of opioid tolerance.
topic Pain
Addiction
epigenetics
opioid
miR
url http://journal.frontiersin.org/Journal/10.3389/fgene.2012.00110/full
work_keys_str_mv AT yingehe let7micrornasandopioidtolerance
AT zaijiejimewang let7micrornasandopioidtolerance
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