Tutorial:The opioid receptor, a molecular switch

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[[Image:Receptor.gif|frame|200|Conceptual model of the opioid receptor. Parts of the receptor between the two cardboard pieces are integrated in the cell membrane, with other parts sticking out and "sticking in"]]
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[[Image:Receptor.gif|frame|200|Conceptual model of the opioid receptor. Parts of the receptor between the two cardboard pieces are integrated in the cell membrane, with other parts sticking out and reaching into the cell]]
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The '''opioid receptor''', a protein on the surface of nerve cells, binds to opioids such as morphine, oxicodone, heroin, and fentanyl. Repeated intake of opioids changes the response to these molecules, and can lead to addiction.
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The '''opioid receptor''', a protein on the surface of nerve cells, binds to opioids such as morphine, oxicodone, heroin, and fentanyl, leading to the inability to feel pain. Repeated intake of opioids changes the response to these molecules, and can lead to addiction.
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== See also ==
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== About this page ==
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This article explains, at a level appropriate to high school students or beginning college students, how the opioid receptor is switched on and off, and what happens inside the brain as a consequence. Other pages related to this topic are:
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This article explains, at a level appropriate to high school students or beginning college students, how the opioid receptor is switched on and off, and what happens inside the brain as a consequence. Five student-made videos accompany this article, and are referenced below. Other pages related to this topic, typically using more technical terms and assuming some prior knowledge in biochemistry, are:
* [[Opioids]]
* [[Opioids]]
* [[Opioid receptor]]
* [[Opioid receptor]]
* [[G protein-coupled receptor]]
* [[G protein-coupled receptor]]
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* [[Mu Opioid Receptor Bound to a Morphinan Antagonist]]
== Relevance ==
== Relevance ==
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== Natural Function ==
== Natural Function ==
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[[Opioid receptor|Opioid receptors]] are proteins found in neurons, the cells that allow us to think, to observe our surroundings with our senses and to move our muscles. Like all cells, neurons have a water-insoluble structure called membrane (or lipid bilayer) surrounding them, keeping molecules from moving into and out of the cell. Opioid receptors are integrated into this membrane with parts reaching out of the cell and parts reaching into the cell, allowing it to act like a switch that is turned on from the outside and affecting the inside of the cell.
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[[Opioid receptor|Opioid receptors]] are proteins found in neurons, the cells that allow us to think, to observe our surroundings with our senses and to move our muscles. Like all cells, neurons have a water-insoluble structure called membrane (or lipid bilayer) surrounding them, keeping molecules from moving into and out of the cell. Opioid receptors are integrated into this membrane with parts reaching out of the cell and parts reaching into the cell, allowing it to act like a switch that is turned on from the outside and affects the inside of the cell.
The human body has different types of opioid receptors called mu, kappa and delta; the mu receptor in particular is responsible for the addictive nature of morphine and other similar opioids involved in the 2010s opioid crisis. A conceptual model of the opioid receptor integrated into the membrane is shown at the top of the page. It shows that the protein is made of a single chain that passes across the membrane multiple times (this structure is shared with a larger group of so-called [[7 pass transmembrane receptors]])
The human body has different types of opioid receptors called mu, kappa and delta; the mu receptor in particular is responsible for the addictive nature of morphine and other similar opioids involved in the 2010s opioid crisis. A conceptual model of the opioid receptor integrated into the membrane is shown at the top of the page. It shows that the protein is made of a single chain that passes across the membrane multiple times (this structure is shared with a larger group of so-called [[7 pass transmembrane receptors]])
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[[Image:Endocytosis.jpg|thumb]]
These opioid receptors interact with opioids via a process known as ligand binding[https://en.wikipedia.org/wiki/Ligand_(biochemistry)#Receptor/ligand_binding_affinity]. When an opioid molecule binds to its receptor, the shape of the receptor changes (a so-called conformational change[https://en.wikipedia.org/wiki/Conformational_change] occurs). This change in the receptor causes it to release a [[GTP-binding protein]] (otherwise known as a G protein), which signals the inside of the cell to behave differently, for example not to cause the sensation of pain. Also, by signalling to other neurons via dopamine binding to the [[dopamine receptor]], large doses of opioids can result in a feeling of pleasure.
These opioid receptors interact with opioids via a process known as ligand binding[https://en.wikipedia.org/wiki/Ligand_(biochemistry)#Receptor/ligand_binding_affinity]. When an opioid molecule binds to its receptor, the shape of the receptor changes (a so-called conformational change[https://en.wikipedia.org/wiki/Conformational_change] occurs). This change in the receptor causes it to release a [[GTP-binding protein]] (otherwise known as a G protein), which signals the inside of the cell to behave differently, for example not to cause the sensation of pain. Also, by signalling to other neurons via dopamine binding to the [[dopamine receptor]], large doses of opioids can result in a feeling of pleasure.
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The part of the receptor that interacts with the G proteins can also bind to another protein in the cell called [[arrestin]]. Arrestin, as its name suggest, stops a given receptor from always being on. When arrestin is bound, the receptor and a bit of the membrane it is integrated in form a small cell-like structure called a vesicle with the opioid binding site pointing inside. Due to increased acidity in the vesicle, the opioid receptor releases the bound opioid. Then, one of two events may occur; either the receptor is delivered back to the cell membrane, or it is broken down into its building blocks.
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The part of the receptor that interacts with the G proteins can also bind to another protein in the cell called [[arrestin]]. Arrestin, as its name suggest, stops a given receptor from always being on. When arrestin is bound, the receptor and a bit of the membrane it is integrated in form a tiny cell-like structure called a vesicle with the opioid binding site pointing inside (see figure at right). Due to increased acidity in the vesicle, the opioid receptor releases the bound opioid. Then, one of two events may occur; either the receptor is delivered back to the cell membrane, or it is broken down into its building blocks.
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To see the receptor in action, you can watch a 4:35 video that connects the activity of an individual with the switching of the receptor in the cell<span class="fas fa-video" style="color:#32CD32"></span>
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To see the physical model of the receptor in action, you can watch a 4:35 min. video [https://www.youtube.com/watch?v=8BcINeVoOWQ (video <span class="fas fa-video" style="color:#338fff"></span>)] that connects the activity of a human individual with the switching of the receptor in the cell.
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[https://www.youtube.com/watch?v=8BcINeVoOWQ]
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== Abuse, overdose and treatment==
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== Tolerance and Abuse==
[[Image:OpioidWaves.JPG|thumb|Structure of oxycodone with a background of the three waves of the Opioid Crisis: 1) Prescription Pain Medication (in gray) 2) Heroin (in orange) 3) Non-Prescribed (Black Market) Fentanyl (in navy)]]
[[Image:OpioidWaves.JPG|thumb|Structure of oxycodone with a background of the three waves of the Opioid Crisis: 1) Prescription Pain Medication (in gray) 2) Heroin (in orange) 3) Non-Prescribed (Black Market) Fentanyl (in navy)]]
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When it comes to opioid addiction, there are several steps involved with how it develops. The first step comes with the initial exposure. As exemplified in this fictional account [https://vimeo.com/377826595 <span class="fas fa-video" style="color:#338fff"></span>], initial exposure can be through prescription medication. While some prescription medications include abuse-deterrent features, these have not prevent prescription drug abuse.[https://www.youtube.com/watch?v=n-azUelCgJg <span class="fas fa-video" style="color:#338fff"></span>].
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When opioids are taken on a regular basis, the body adapts and shows less of a reaction. This is called [https://en.wikipedia.org/wiki/Drug_tolerance tolerance]. Once someone is tolerant to opioids, a higher dose is necessary to give the same pain relief. Tolerance also lowers the dopamine-releasing effects brought about by the presence of opioids in the body. The interaction between opioid receptor and arrestin, discussed in the previous section, is thought to play a role in tolerance. The adaptations in the body also are responsible for [https://en.wikipedia.org/wiki/Drug_withdrawal withdrawal] when not taking opioids for a while, inflicting crippling side-effects and cravings for the next drug dose. Going through multiple cycles of drug intake, withdrawal and craving can lead to a harmful behavior of seeking drugs even though the patient is aware of the dangers of overdose and the toll addiction has on an individual and their community.
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Once an individual takes an opioid medication, the aforementioned process transpires. When the arrestin begins to alter the cell's environment, it has with it a secondary effect. The process arrestin causes also develops drug tolerance[https://en.wikipedia.org/wiki/Drug_tolerance], which makes the body more resistant to the pain-numbing and dopamine-releasing effects brought about by the presence of opioids in the body. Furthermore, the psychological impact of low pain and high dopamine result in the body desiring this effect from said opioids. Altogether, this sets the body up to take more and more opioids to get this feeling, and, in turn, building more and more tolerance. Attempting to go off of the drugs by this point results in withdrawal[https://en.wikipedia.org/wiki/Drug_withdrawal], which throws off the body's systems and the chemicals in the brain, altering personality and inflicting crippling side-effects.
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This fictional account [https://vimeo.com/377826595 (video <span class="fas fa-video" style="color:#338fff"></span>)] tells a story of how initial exposure through prescribed medication leads to medication abuse and to switching to the even more addictive drug heroin. While some prescription medications include abuse-deterrent features, these have not prevented prescription drug abuse.[https://www.youtube.com/watch?v=n-azUelCgJg (video <span class="fas fa-video" style="color:#338fff"></span>)] .
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When untreated, opioid overdose kills people because they stop breathing. The drug naloxone[https://en.wikipedia.org/wiki/Naloxone] can prevent overdose deaths when administered in time. [https://youtu.be/_LFWsDXLnkI <span class="fas fa-video" style="color:#338fff"></span>]
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==Overdose and Treatment==
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When untreated, opioid overdose kills people because they stop breathing. The drug naloxone[https://en.wikipedia.org/wiki/Naloxone] can prevent overdose deaths when administered in time [https://youtu.be/_LFWsDXLnkI (video)]<span class="fas fa-video" style="color:#338fff"></span>.
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The continual presence of opioids in the body can have with it other effects. Within pregnant mothers, it may result in what is known as Neonatal Abstinence Syndrome (NAS) [https://www.youtube.com/watch?v=gxQcXtS6lG4 <span class="fas fa-video" style="color:#338fff"></span>], in which the fetus develops withdrawal symptoms after birth. This is due to the drugs passing through the placenta into the newborn's body prior to birth. Essentially, the infant becomes addicted before even being born, which, in turn, inflicts a myriad of health complications, some of which possibly fatal.
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When pregnant mothers take opioids, either self-administered or as part of a opioid maintenance therapy, the fetus will be exposed to the opioids and will become tolerant before birth. At birth, the baby may experience what is called Neonatal Abstinence Syndrome (NAS) [https://www.youtube.com/watch?v=gxQcXtS6lG4 (video)]<span class="fas fa-video" style="color:#338fff"></span>, in which the baby develops withdrawal symptoms after the supply of opioids via the umbilical chord is cut off. The withdrawal after birth inflicts a myriad of health complications. However, if medical support is available and the condition is diagnosed in time, there are multiple treatment options that help the baby to transition to an opioid-free life.
== Structural highlights ==
== Structural highlights ==
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Try rotating the molecule after turning off the automatic spinning (+/- spin button). Zooming in on the <scene name='83/830406/Peptide/2'>signalling molecule</scene>, you see it is deeply buried within the protein. Binding results in a change of shape of the receptor (not shown here) to relay the signal to the inside of the cell.
Try rotating the molecule after turning off the automatic spinning (+/- spin button). Zooming in on the <scene name='83/830406/Peptide/2'>signalling molecule</scene>, you see it is deeply buried within the protein. Binding results in a change of shape of the receptor (not shown here) to relay the signal to the inside of the cell.
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In the 21st century opioid crisis in the USA, the crisis started with prescription opioids like <jmol><jmolLink><script> background image "http://proteopedia.org/wiki/images/6/66/OpioidFatality2.JPG"; load $oxycodone; select _C; color mediumpurple; hide _H; moveto 1.0 { -1000 21 -14 66.69} 46.78 -22.06 -16.47 {-0.81575 0.02959999999999985 -0.13314999999999988} 7.056706882620149 {0 0 0} 0 0 0 3.0 0.0 0.0; set zshade on; set zshadepower 1</script><text>oxycodone</text></jmolLink> </jmol>, then transitioned to use of <jmol><jmolLink><script>load $heroin; select _C; color orange; hide _H; set zshade on; set zshadepower 1</script><text>heroin</text></jmolLink></jmol>, and was made worse when street drugs started to by mixed with <jmol><jmolLink><script>background image "http://proteopedia.org/wiki/images/6/66/OpioidFatality4.JPG"; load $fentanyl; select _C; color black; hide _H; set zshade on; set zshadepower 1</script><text>fentanyl</text></jmolLink></jmol>.
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In the 21st century opioid crisis in the USA, the crisis started with prescription opioids like <jmol><jmolLink><script> set refreshing false; load $oxycodone; background image "http://proteopedia.org/wiki/images/6/66/OpioidFatality2.JPG"; select _C; color mediumpurple; hide _H; moveto 1.0 { -977 204 68 164.66} 5.0 -34.67 36.52 {-0.1478 -0.08705 0.2597} 7.521992 {0 0 0} 0 0 0 3.0 0.0 0.0; set refreshing true; moveto 1.0 { -1000 21 -14 66.69} 46.78 -22.06 -16.47 {-0.81575 0.02959999999999985 -0.13314999999999988} 7.056706882620149 {0 0 0} 0 0 0 3.0 0.0 0.0; set zshade on; set zshadepower 1; set spinY 0; set spinX 90; spin on;</script><text>oxycodone</text></jmolLink> </jmol>, then transitioned to use of <jmol><jmolLink><script>set refreshing false; load $heroin; background image "http://proteopedia.org/wiki/images/e/e6/OpioidFatality3.JPG"; select _C; color orange; hide _H; set zshade on; set zshadepower 1; moveto 1.0 { 970 216 -113 30.11} 5.0 -8.1 36.32 {-0.1478 -0.08705 0.2597} 7.521992 {0 0 0} 0 0 0 3.0 0.0 0.0; set refreshing true; moveto 1.0 { 997 68 23 122.37} 42.42 3.87 -19.17 {-0.1478 -0.08705 0.2597} 7.521992 {0 0 0} 0 0 0 3.0 0.0 0.0; set spinY 0; set spinX 90; spin on;</script><text>heroin</text></jmolLink></jmol>, and was made worse when street drugs started to by mixed with <jmol><jmolLink><script>set refreshing false; load $fentanyl; select _C; color black; hide _H; set zshade on; set zshadepower 1; background image "http://proteopedia.org/wiki/images/5/51/OpioidFatality4.JPG"; moveto 1.0 { 802 6 -597 24.36} 5.1 32.85 34.38 {-1.40835 0.0738 -0.28485} 9.158728 {0 0 0} 0 0 0 3.0 0.0 0.0;; set refreshing true; moveto 1.0 { -997 -67 -31 130.64} 55.02 -9.39 -19.75 {-1.40835 0.0738 -0.28485} 9.158728 {0 0 0} 0 0 0 3.0 0.0 0.0; set spinY 0; set spinX 90; spin on;</script><text>fentanyl</text></jmolLink></jmol>.
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When naloxone is administered to reverse an overdose, it competes with <scene name='83/830406/Competition/1'>the opioid agonist bound to the receptor</scene>. Every couple of minutes, an agonist molecule will leave the binding site. In the absence of naloxone, another agonist will bind (or the <jmol><jmolLink><script>ago0 = [ {-27.674 -8.743 -15.007},{-27.434 -7.353 -14.448},{-26.336 -8.407 -14.33},{-25.984 -8.850999999999999 -12.878},{-25.934 -10.308 -12.595},{-25.51 -10.46 -11.222},{-25.414 -11.906 -10.78},{-26.812 -12.526 -10.96},{-27.699 -11.843 -10.09},{-26.844 -13.782 -10.383},{-26.608 -13.297 -9},{-27.656 -12.441 -8.864},{-28.181 -11.619 -7.974},{-28.156 -12.113 -6.708},{-29.107 -10.618 -8.263},{-29.238 -10.14 -9.555},{-28.429 -10.775 -10.475},{-28.499 -10.494 -11.86},{-27.259 -10.996 -12.682},{-27.26 -12.476 -12.41},{-26.332 -13.147 -13.263},{-28.656 -13.091 -12.522},{-28.674 -14.519 -12.044},{-28.226 -14.446 -10.537},{-28.194 -15.779 -9.909},{-29.302 -16.538 -9.812},{-30.419 -16.187 -10.19},{-29.118 -17.898 -9.138},{-30.172 -18.853 -9.723},{-30.053 -19.003 -11.252},{-31.056 -19.22 -11.934},{-28.801 -18.878 -11.772},{-28.86 -19.034 -13.196} ]
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To explore how naloxone reverses an overdose, let's look at the situation during an overdose. The opioid receptor binding pocket is occupied by <scene name='83/830406/Competition/2'>the opioid agonist</scene>. Every couple of minutes, an agonist molecule will leave the binding site. In the absence of naloxone, another agonist will bind (or the <jmol><jmolLink><script>ago0 = [ {-27.674 -8.743 -15.007},{-27.434 -7.353 -14.448},{-26.336 -8.407 -14.33},{-25.984 -8.850999999999999 -12.878},{-25.934 -10.308 -12.595},{-25.51 -10.46 -11.222},{-25.414 -11.906 -10.78},{-26.812 -12.526 -10.96},{-27.699 -11.843 -10.09},{-26.844 -13.782 -10.383},{-26.608 -13.297 -9},{-27.656 -12.441 -8.864},{-28.181 -11.619 -7.974},{-28.156 -12.113 -6.708},{-29.107 -10.618 -8.263},{-29.238 -10.14 -9.555},{-28.429 -10.775 -10.475},{-28.499 -10.494 -11.86},{-27.259 -10.996 -12.682},{-27.26 -12.476 -12.41},{-26.332 -13.147 -13.263},{-28.656 -13.091 -12.522},{-28.674 -14.519 -12.044},{-28.226 -14.446 -10.537},{-28.194 -15.779 -9.909},{-29.302 -16.538 -9.812},{-30.419 -16.187 -10.19},{-29.118 -17.898 -9.138},{-30.172 -18.853 -9.723},{-30.053 -19.003 -11.252},{-31.056 -19.22 -11.934},{-28.801 -18.878 -11.772},{-28.86 -19.034 -13.196} ]
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Line 120: Line 122:
</StructureSection>
</StructureSection>
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 +
== Further reading ==
 +
 +
* [https://ny.pbslearningmedia.org/resource/nva-sci-collectionguide/ NOVA: Addiction]: A teaching guide answering frequently asked questions about opioid abuse and treatment.
 +
* [https://www.nejm.org/doi/full/10.1056/nejmra1507771 Review article] on prescription opioid use and abuse by Nora Volkow and Thomas McLellan
 +
* [https://www.ncbi.nlm.nih.gov/books/NBK22592/ Membrane receptor and G-proteins]: Chapter in the Berg/Tymoczko/Stryer Biochemistry textbook on membrane receptors and events mediated by G-proteins inside the cell.
 +
* [https://www.oercommons.org/courseware/lesson/60267 Lesson plan] for a discussion based on five student-made videos

Current revision

Conceptual model of the opioid receptor. Parts of the receptor between the two cardboard pieces are integrated in the cell membrane, with other parts sticking out and reaching into the cell
Conceptual model of the opioid receptor. Parts of the receptor between the two cardboard pieces are integrated in the cell membrane, with other parts sticking out and reaching into the cell

The opioid receptor, a protein on the surface of nerve cells, binds to opioids such as morphine, oxicodone, heroin, and fentanyl, leading to the inability to feel pain. Repeated intake of opioids changes the response to these molecules, and can lead to addiction.

Contents

About this page

This article explains, at a level appropriate to high school students or beginning college students, how the opioid receptor is switched on and off, and what happens inside the brain as a consequence. Five student-made videos accompany this article, and are referenced below. Other pages related to this topic, typically using more technical terms and assuming some prior knowledge in biochemistry, are:

Relevance

When we want to turn on the lights in a dark room, we don't have to climb up a ladder to screw in a light bulb. All we have to do is flip a switch. A biological cell has switches, too, called receptors. Most are on the cell surface with a part sticking out, ready to bind to a signaling molecule. Another part of the receptor reaches into the inside of the cell, transmitting the signal. The opioid receptor can be switched on to relieve pain, for example during surgery. Tragically, it is very easy to become physically dependent on the signaling molecules. The ongoing opioid crisis in the USA shows how addictive opioids are (e.g. morphine, oxicodone, heroin, and fentanyl), with overdose deaths decreasing average life expectancy across the US population significantly.

Natural Function

Opioid receptors are proteins found in neurons, the cells that allow us to think, to observe our surroundings with our senses and to move our muscles. Like all cells, neurons have a water-insoluble structure called membrane (or lipid bilayer) surrounding them, keeping molecules from moving into and out of the cell. Opioid receptors are integrated into this membrane with parts reaching out of the cell and parts reaching into the cell, allowing it to act like a switch that is turned on from the outside and affects the inside of the cell.

The human body has different types of opioid receptors called mu, kappa and delta; the mu receptor in particular is responsible for the addictive nature of morphine and other similar opioids involved in the 2010s opioid crisis. A conceptual model of the opioid receptor integrated into the membrane is shown at the top of the page. It shows that the protein is made of a single chain that passes across the membrane multiple times (this structure is shared with a larger group of so-called 7 pass transmembrane receptors)

These opioid receptors interact with opioids via a process known as ligand binding[1]. When an opioid molecule binds to its receptor, the shape of the receptor changes (a so-called conformational change[2] occurs). This change in the receptor causes it to release a GTP-binding protein (otherwise known as a G protein), which signals the inside of the cell to behave differently, for example not to cause the sensation of pain. Also, by signalling to other neurons via dopamine binding to the dopamine receptor, large doses of opioids can result in a feeling of pleasure.

The part of the receptor that interacts with the G proteins can also bind to another protein in the cell called arrestin. Arrestin, as its name suggest, stops a given receptor from always being on. When arrestin is bound, the receptor and a bit of the membrane it is integrated in form a tiny cell-like structure called a vesicle with the opioid binding site pointing inside (see figure at right). Due to increased acidity in the vesicle, the opioid receptor releases the bound opioid. Then, one of two events may occur; either the receptor is delivered back to the cell membrane, or it is broken down into its building blocks.

To see the physical model of the receptor in action, you can watch a 4:35 min. video (video ) that connects the activity of a human individual with the switching of the receptor in the cell.

Tolerance and Abuse

Structure of oxycodone with a background of the three waves of the Opioid Crisis: 1) Prescription Pain Medication (in gray) 2) Heroin (in orange) 3) Non-Prescribed (Black Market) Fentanyl (in navy)
Structure of oxycodone with a background of the three waves of the Opioid Crisis: 1) Prescription Pain Medication (in gray) 2) Heroin (in orange) 3) Non-Prescribed (Black Market) Fentanyl (in navy)

When opioids are taken on a regular basis, the body adapts and shows less of a reaction. This is called tolerance. Once someone is tolerant to opioids, a higher dose is necessary to give the same pain relief. Tolerance also lowers the dopamine-releasing effects brought about by the presence of opioids in the body. The interaction between opioid receptor and arrestin, discussed in the previous section, is thought to play a role in tolerance. The adaptations in the body also are responsible for withdrawal when not taking opioids for a while, inflicting crippling side-effects and cravings for the next drug dose. Going through multiple cycles of drug intake, withdrawal and craving can lead to a harmful behavior of seeking drugs even though the patient is aware of the dangers of overdose and the toll addiction has on an individual and their community.

This fictional account (video ) tells a story of how initial exposure through prescribed medication leads to medication abuse and to switching to the even more addictive drug heroin. While some prescription medications include abuse-deterrent features, these have not prevented prescription drug abuse.(video ) .

Overdose and Treatment

When untreated, opioid overdose kills people because they stop breathing. The drug naloxone[3] can prevent overdose deaths when administered in time (video).

When pregnant mothers take opioids, either self-administered or as part of a opioid maintenance therapy, the fetus will be exposed to the opioids and will become tolerant before birth. At birth, the baby may experience what is called Neonatal Abstinence Syndrome (NAS) (video), in which the baby develops withdrawal symptoms after the supply of opioids via the umbilical chord is cut off. The withdrawal after birth inflicts a myriad of health complications. However, if medical support is available and the condition is diagnosed in time, there are multiple treatment options that help the baby to transition to an opioid-free life.

Structural highlights

Drag the structure with the mouse to rotate

Further reading

  • NOVA: Addiction: A teaching guide answering frequently asked questions about opioid abuse and treatment.
  • Review article on prescription opioid use and abuse by Nora Volkow and Thomas McLellan
  • Membrane receptor and G-proteins: Chapter in the Berg/Tymoczko/Stryer Biochemistry textbook on membrane receptors and events mediated by G-proteins inside the cell.
  • Lesson plan for a discussion based on five student-made videos

Proteopedia Page Contributors and Editors (what is this?)

Karsten Theis, Cameron Young

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