PathWhiz ID | Pathway | Meta Data |
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PW126801View Pathway |
drug action
Cocaine Analgesic Action PathwayHomo sapiens
Cocaine is a local anesthesia and vasoconstrictor that is clinically used during diagnostic proceedures or during surgery in or through the nasal cavity. It comes in drugs called Goprelto and Numbrino which comes as a nasal spray. In these clinical drugs it takes the form of cocaine hydrochloride. The illicit drug has the same effects.
Primarily it acts on sensory neurons in the nasal cavity by inhibiting the sodium channels. Stimulation from touch, pressure, stretch, or pain causes sodium channels on sensory receptors to open. Cocaine inhibits those channels, preventing the sensory receptor from depolarizing and triggering an action potential. The different types of sensory neurons it inhibits are mechanoreceptors(pressure, vibrations, and texture), thermoreceptors (temperature), and nociceptors (pain). The prevention of depolarization and action potential in these neurons causes an anesthetic effect in the nasal cavity.
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Creator: Ray Kruger Created On: March 30, 2022 at 13:45 Last Updated: March 30, 2022 at 13:45 |
PW128143View Pathway |
drug action
Cocaine Dopamine-reuptake Inhibitor Action PathwayHomo sapiens
Cocaine is a local anesthesia and vasoconstrictor that is clinically used during diagnostic proceedures or during surgery in or through the nasal cavity. It comes in drugs called Goprelto and Numbrino which comes as a nasal spray. In these clinical drugs it takes the form of cocaine hydrochloride. The illicit drug has the same effects. It primarily acts on sensory neurons in the nasal cavity, but also inhibits dopamine, serotonin, and norepinephrine re-uptake channels.
This inibition leads to an accumulation in the synapse of these neurotransmitters. For dopamine this leads to activation of dopamine receptors, especially the D2 dopamine receptor which has been implicated in the cause of addiction through the reward pathway. D2 receptors inhibit adenylate cyclase which leads to a lower concentration of cAMP which lowers neuronal excitability. Other dopamine receptors also have an effect on addiction,, especially the D1 dopamine receptor. The exact mechanisms in which D2 receptors cause addiction is unknown. D1 dopamine receptors also have an effect on addiction. They are Gs coupled and activated adenylate cyclase rather than inhibit. D1-D2 dopamine receptor heteromers have also been found to effect addiction, although they have not been researched enough to understand how.
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Creator: Ray Kruger Created On: July 24, 2023 at 15:47 Last Updated: July 24, 2023 at 15:47 |
PW124081View Pathway |
drug action
Cocaine Drug Action Action Pathway (New)Homo sapiens
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Creator: Nitya Khetarpal Created On: August 15, 2020 at 19:31 Last Updated: August 15, 2020 at 19:31 |
PW124082View Pathway |
drug action
Cocaine Drug Action Action Pathway (New) -- DISCARDEDHomo sapiens
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Creator: Nitya Khetarpal Created On: August 15, 2020 at 19:43 Last Updated: August 15, 2020 at 19:43 |
PW145008View Pathway |
drug action
Cocaine Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 14:54 Last Updated: October 07, 2023 at 14:54 |
PW126809View Pathway |
Cocaine metabolismHomo sapiens
Cocaine is a local anaesthetic used for diagnostic procedures or surgery on or through the nasal cavity. It is administered as a spray in the nose where it enters the blood vessels of the nose and travels through the body. When taken illicitly it is snorted through the nose and enters through the same blood vessels. Cocaine is metabolized in hepatic liver cells. Cocaine diffuses through the liver membrane. On the endoplasmic reticulum membrane it is metabolized by cytochrome P450 3A4 into norcocaine. It is also predicted by biotransformer to metabolize by cytochrome P450 1A2 into benzoylecgonine. Both of these metabolites are inactive and the main metabolite when cocaine is taken on its own. When cocaine is taken with alcohol however, it metabolizes into the active metabolite cocaethylene by the hepatic enzyme carboxylesterase in the endoplasmic reticulum lumen. Norcocaine, benzoylecogonine, and cocaethylene all diffuse through the hepatic cell membrane into the blood where they travel to the kidney and are excreted renally. However, cocaethylene is an active metabolite that is much more toxic than cocaine and has a higher affinity for dopamine re-uptake receptors, and therefore will activate similar pathways to cocaine. It takes much longer for it to be excreted renally than cocaine. Cocaethylene is often fatal.
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Creator: Ray Kruger Created On: March 31, 2022 at 15:40 Last Updated: March 31, 2022 at 15:40 |
PW128144View Pathway |
drug action
Cocaine Norepinephrine Reuptake Inhibitor Action PathwayHomo sapiens
Cocaine is a local anesthesia and vasoconstrictor that is clinically used during diagnostic proceedures or during surgery in or through the nasal cavity. It comes in drugs called Goprelto and Numbrino which comes as a nasal spray. In these clinical drugs it takes the form of cocaine hydrochloride. The illicit drug has the same effects. It primarily acts on sensory neurons in the nasal cavity, but also inhibits dopamine, serotonin, and norepinephrine re-uptake channels.
Cocaine inhibits the sodium-dependent noradrenaline channel which causes norepinephrine to accumulate in the synapse. The high concentration of norepinephrine readily activates both alpha adrenergic receptors in the smooth muscles of blood vessels. This, through the Gq signalling cascade, leads to vasoconstriction of blood vessels especially in the nose. This also causes higher heart rate and higher blood pressure, due to vasoconstriction, in the rest of the body as seen in the norepinephrine subpathway.
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Creator: Ray Kruger Created On: July 24, 2023 at 15:48 Last Updated: July 24, 2023 at 15:48 |
PW145504View Pathway |
drug action
Cocarboxylase Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 15:57 Last Updated: October 07, 2023 at 15:57 |
PW000411View Pathway |
drug action
Codeine Action PathwayHomo sapiens
Opiate receptors are coupled with G-protein receptors and function as both positive and negative regulators of synaptic transmission via G-proteins that activate effector proteins. Binding of the opiate stimulates the exchange of GTP for GDP on the G-protein complex. As the effector system is adenylate cyclase and cAMP located at the inner surface of the plasma membrane, opioids decrease intracellular cAMP by inhibiting adenylate cyclase. Subsequently, the release of nociceptive neurotransmitters such as substance P, GABA, dopamine, acetylcholine and noradrenaline is inhibited. Opioids also inhibit the release of vasopressin, somatostatin, insulin and glucagon. Codeine's analgesic activity is, most likely, due to its conversion to morphine. Opioids close N-type voltage-operated calcium channels (OP2-receptor agonist) and open calcium-dependent inwardly rectifying potassium channels (OP3 and OP1 receptor agonist). This results in hyperpolarization and reduced neuronal excitability.
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Creator: WishartLab Created On: August 22, 2013 at 10:46 Last Updated: August 22, 2013 at 10:46 |
PW144445View Pathway |
drug action
Codeine Drug Metabolism Action PathwayHomo sapiens
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Creator: Ray Kruger Created On: October 07, 2023 at 13:39 Last Updated: October 07, 2023 at 13:39 |