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PathWhiz ID Pathway Meta Data

PW126801

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drug action

Cocaine Analgesic Action Pathway

Homo 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.

PW128143

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drug action

Cocaine Dopamine-reuptake Inhibitor Action Pathway

Homo 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.

PW124081

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drug action

Cocaine Drug Action Action Pathway (New)

Homo sapiens

PW124082

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drug action

Cocaine Drug Action Action Pathway (New) -- DISCARDED

Homo sapiens

PW145008

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drug action

Cocaine Drug Metabolism Action Pathway

Homo sapiens

PW126809

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metabolic

Cocaine metabolism

Homo 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.

PW128144

Pw128144 View Pathway
drug action

Cocaine Norepinephrine Reuptake Inhibitor Action Pathway

Homo 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.

PW145504

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drug action

Cocarboxylase Drug Metabolism Action Pathway

Homo sapiens

PW000411

Pw000411 View Pathway
drug action

Codeine Action Pathway

Homo 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.

PW144445

Pw144445 View Pathway
drug action

Codeine Drug Metabolism Action Pathway

Homo sapiens