CNS Stimulants Cerebral Stimulants (Psychostimulants ) Hallucinogens Analeptics or Convulsants
Adrenergic Agentspharmacy.uokerbala.edu.iq/wp/wp-content/uploads/2014/10... · 2017. 4. 11. ·...
Transcript of Adrenergic Agentspharmacy.uokerbala.edu.iq/wp/wp-content/uploads/2014/10... · 2017. 4. 11. ·...
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Adrenergic Agents
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Adrenergic Agents
•Agonists
• Sympathomimetics
•Adrenergic stimulants
•Adrenergic agonists
•Antagonists
• Sympatholytics
•Antiadrenergics, or
•Adrenergic-blocking agents
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Endogenous Catecholamines (Adrenergic Neurotransmitters)
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Dopamine
•Differs from NE in lacking of 1-OH group.
• It is the immediate precursor of NE.
•Regarding the structure of dopamine, dopamine has a short DOA with no oral activity. Explain why?
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Norepinephrine (NE)
• Differs from DA only by addition of a 1-OH substituent.
• Differs from E only by lacking the N -methyl group.
• Like DA, it is polar and rapidly metabolized by both COMT and MAO, resulting in poor oral bioavailability and short DOA (1 or 2 minutes even when given intravenously).
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Epinephrine (E, Adrenalin)
• Differs from NE by the addition of an N -methyl group.
• Like the other CAs, E is light sensitive and easily oxidized on exposure to air because of the catechol ring system.
• The development of a pink-to-brown color indicates oxidative breakdown.
• To minimize oxidation, solutions of the drug are stabilized by the addition of reducing agents such as sodium bisulfite
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DRUGS AFFECTING ADRENERGIC NEUROTRANSMISSION:
A.Drugs Affecting Catecholamine Biosynthesis
B. Drugs Affecting Catecholamine Storage and Release
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Drugs Affecting Catecholamine Biosynthesis
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Metyrosine:
• Metyrosine is a much more effective competitive inhibitor of E and NE production than agents that inhibit any of the other enzymes involved in CA biosynthesis. Why?
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Drugs Affecting Catecholamine Storage and Release
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Reserpine
•Reserpine is an indole alkaloid obtained from the root of Rauwolfia serpentina found in India.
•Reserpine is known as “NT Depleter”. Explain why?
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Guanethidine and guanadrel
• These drugs bind to the storage vesicles and stabilize the neuronal storage vesicle membranes, making them less responsive to nerve impulses.
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References:
• Wilson and Gisvold Textbook of Organic
Medicinal and Pharmaceutical Chemistry;
Delgado JN, Remers WA, (Eds.); 12th ed., 2011.
• https://pubchem.ncbi.nlm.nih.gov/search/sea
rch.cgi
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