Dr. Brown (Outlined) - Website of Neelay Gandhi
... Amygdala: emotion, learning (especially for fear associated learning) Hypothalamus: four F’s (feeding, fighting, flighting, fucking) ...
... Amygdala: emotion, learning (especially for fear associated learning) Hypothalamus: four F’s (feeding, fighting, flighting, fucking) ...
`drug`.
... The drug must fit into the Binding Site and shape complementarity is an important feature of a drug molecule. Competitive enzyme inhibitors often bear a resemblance to the substrate, as they bind to the same Active Site. This is also true for some receptor antagonists, but not all. The strength of a ...
... The drug must fit into the Binding Site and shape complementarity is an important feature of a drug molecule. Competitive enzyme inhibitors often bear a resemblance to the substrate, as they bind to the same Active Site. This is also true for some receptor antagonists, but not all. The strength of a ...
Side effects
... inhaled or oral administration and have got longer duration of action. They are the most widely used sympathomimetics. Commonly used drugs both by oral and inhalation are Salbutamol, terbutaline, metaproterenol, pirbuterol and bitolterol. Salmeterol and formeterol are new generation, long acting β2- ...
... inhaled or oral administration and have got longer duration of action. They are the most widely used sympathomimetics. Commonly used drugs both by oral and inhalation are Salbutamol, terbutaline, metaproterenol, pirbuterol and bitolterol. Salmeterol and formeterol are new generation, long acting β2- ...
Pharmacodynamics – How Drugs Work
... The action of an endogenous agonist is enhanced if its release is increased. For example, amphetamines increase the release of monoamines, such as dopamine, from nerve terminals. Because amphetamines can cause a syndrome similar to schizophrenia, this action has led to the idea that schizophrenia ma ...
... The action of an endogenous agonist is enhanced if its release is increased. For example, amphetamines increase the release of monoamines, such as dopamine, from nerve terminals. Because amphetamines can cause a syndrome similar to schizophrenia, this action has led to the idea that schizophrenia ma ...
Midterm review - February 26, 2004
... Anesthetics come in two basic chemical flavors. They are composed of an aromatic group linked to an amine by either an ester bond or an amide bond. Esters: Procaine, Tetracaine, Benzocaine (topical), Cocaine (vasoconstrictor!) Amides: Bupivicaine, Lidocaine, Mepivacaine, Etidocaine (amides always ha ...
... Anesthetics come in two basic chemical flavors. They are composed of an aromatic group linked to an amine by either an ester bond or an amide bond. Esters: Procaine, Tetracaine, Benzocaine (topical), Cocaine (vasoconstrictor!) Amides: Bupivicaine, Lidocaine, Mepivacaine, Etidocaine (amides always ha ...
Terms and symbols - Guide to Pharmacology
... to use an interim nomenclature based on the individual subunits (Spedding et al., 2002). Nevertheless, the ultimate goal is to define the multi-subunit assemblies that occur in vivo. The regions of the receptor macromolecule to which ligands bind are referred to collectively as the recognition site( ...
... to use an interim nomenclature based on the individual subunits (Spedding et al., 2002). Nevertheless, the ultimate goal is to define the multi-subunit assemblies that occur in vivo. The regions of the receptor macromolecule to which ligands bind are referred to collectively as the recognition site( ...
Drug Targets
... 3. In most cases the initial interactions between the enzyme and the substrate molecule (i.e., the initial binding event) are noncovalent, making use of hydrogen bonding, electrostatic, hydrophobic interactions, and van der Waals forces to effect binding. 4. The active site of enzymes usually are lo ...
... 3. In most cases the initial interactions between the enzyme and the substrate molecule (i.e., the initial binding event) are noncovalent, making use of hydrogen bonding, electrostatic, hydrophobic interactions, and van der Waals forces to effect binding. 4. The active site of enzymes usually are lo ...
Midterm review - February 26, 2004
... Anesthetics come in two basic chemical flavors. They are composed of an aromatic group linked to an amine by either an ester bond or an amide bond. Esters: Procaine, Tetracaine, Benzocaine (topical), Cocaine (vasoconstrictor!) Amides: Bupivicaine, Lidocaine, Mepivacaine, Etidocaine (amides always ha ...
... Anesthetics come in two basic chemical flavors. They are composed of an aromatic group linked to an amine by either an ester bond or an amide bond. Esters: Procaine, Tetracaine, Benzocaine (topical), Cocaine (vasoconstrictor!) Amides: Bupivicaine, Lidocaine, Mepivacaine, Etidocaine (amides always ha ...
Nicotine Pharmacology and Principles of
... Nicotine is readily absorbed through intact skin. Nicotine is well absorbed in the small intestine but has low bioavailability (20-45%) due to first-pass hepatic metabolism. ...
... Nicotine is readily absorbed through intact skin. Nicotine is well absorbed in the small intestine but has low bioavailability (20-45%) due to first-pass hepatic metabolism. ...
core modules & forms of tobacco
... Nicotine is readily absorbed through intact skin. Nicotine is well absorbed in the small intestine but has low bioavailability (20-45%) due to first-pass hepatic metabolism. ...
... Nicotine is readily absorbed through intact skin. Nicotine is well absorbed in the small intestine but has low bioavailability (20-45%) due to first-pass hepatic metabolism. ...
Pharmacology Block 3 Notes Autonomic Pharmacology I
... Example: a neurotransmitter binds to a receptor and increases that receptor’s activity (thus serving as an agonist); however when this receptor is activated, the activity of the neuron is decreased (generating an inhibitory effect) The receptor is thus an INHIBITORY RECEPTOR This is how molecule ...
... Example: a neurotransmitter binds to a receptor and increases that receptor’s activity (thus serving as an agonist); however when this receptor is activated, the activity of the neuron is decreased (generating an inhibitory effect) The receptor is thus an INHIBITORY RECEPTOR This is how molecule ...
Nicotinic agonist
A nicotinic agonist is a drug that mimics the action of acetylcholine (ACh) at nicotinic acetylcholine receptors (nAChRs). The nAChR is named for its affinity for nicotine.Examples include nicotine (by definition), acetylcholine (the endogenous agonist of nAChRs), choline, epibatidine, lobeline, varenicline and cytisine.