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DƯỢC LÍ Goodman & Gilman's The Pharmacological Basis of Therapeutics 12th, 2010

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2020

INDEX

Diuretics (Cont.):

inhibitors of Na + -CI − symport, 678t,

686–690, 688t

inhibitors of Na + -K + -2CI − symport,

678t, 682–686, 683t

inhibitors of nonspecific cation

channel, 695–696

inhibitors of renal epithelial sodium

channels, 678t, 690–692,

690t

intolerance, 701

loop (See Loop diuretics)

mechanism of action of, 697f

and organic acid and organic base

secretion, 676, 676f

osmotic (See Osmotic diuretics)

polymorphisms and response to,

160t

potassium-sparing, 690–692, 690t

as antihypertensive agents, 774t,

778

chemistry of, 690, 690t

drug interactions with, 691–692

excretory and renal hemodynamic

effects of, 678t, 691

mechanism of action of, 690–691,

691f

pharmacology of, 690t

and renal hemodynamics, 691

site of action of, 690–691

structure of, 690t

therapeutic uses of, 692

toxicity, adverse effects, and

contraindications to,

691–692

and urinary excretion, 691

renal epithelial transport and,

674–676

renal handling of specific anions and

cations and, 676–677

resistance (edema refractory to),

699

role in clinical medicine, 698–701

site of action of, 697f

therapeutic uses of, Brater’s

algorithm for, 699, 700f

thiazide (See Thiazide diuretics)

thiazide, SLC transporters and, 102t

DIURIL (chlorothiazide), 688t, 791

Diversity, ethnic, 150–151

DIVIGEL (estradiol), 1839t

DMPP. See

Dimethylphenylpiperazinium

(DMPP)

DNA methylation, 97

Dobutamine

adrenergic receptors and, 206t

adverse effects of, 290, 321t

cardiovascular effects of, 290

pharmacological properties of, 321t

structure of, 279t

therapeutic uses of, 290, 321t

for heart failure, 804–805

Docetaxel, 1668t–1670t

pharmacokinetics of, 1832t

Docosanol, 1596t, 1604

for cutaneous viral infections, 1818

Docusate, 1330t

Dofetilide, 839

adverse effects of, 839

arrhythmias caused by, 821t

contraindications to, 833t

dosage and administration of, 835t

electrophysiological actions of, 829t

mechanism of action of, 830

pharmacokinetics of, 835t, 839

structure of, 839

Dolasetron, arrhythmias caused by,

832

Domperidone, 1326

Donepezil

for Alzheimer’s, 253

pharmacokinetics of, 1833t

structure of, 243f

Donor cell chimerism, 1021

Dopa, in catecholamine synthesis, 194f

DOPAC. See 3,4-dihydroxyphenyl

acetic acid (DOPAC)

Dopa decarboxylase, 195

Dopamine

therapeutic uses of, for heart failure,

804

and vasopressin secretion, 704

Dopamine beta-hydroxylase (DβH),

194, 195

Dopamine beta-hydroxylase

deficiency, 195

Dopamine (DA)

addiction and, 357

antipsychotics and, 427t

in behavior, 356–357

cardiovascular effects of, 288

catecholamine release and, 355

in central nervous system, 382

central nervous system and,

355–356

chemistry, 351

cognition and, 357

heart and, 355

history of, 351

Dopamine (DA) (Cont.):

kidneys and, 355

learning and, 357

memory and, 357

metabolism of, 351–353

Parkinson disease and, 356–357

pharmacology of, 288

physiological functions of, 353–359

pituitary gland and, 355

precautions, adverse reactions, and

contraindications to, 288

sources of, 351

structure of, 279t

synthesis of, 194–196, 351–353

therapeutic uses of, 288–289, 290

vasculature and, 355

Dopamine hypothesis, 417

Dopamine receptor(s)

agonists, 357–358, 616–617,

1114–1115

antagonists, 358–359, 1325–1326

for nausea, 1343

antipsychotics and, 427t

D 2

, 427t

Dopaminergic agonists, therapeutic

uses of, for heart failure,

804–805

Dopamine transporter, antidepressant

potencies at, 406t

Dopamine transporter (DAT), 116,

198t

polymorphisms in, 150f

DOPEG. See 3,4-dihydroxyphenyl

glycol (DOPEG)

DOPET. See 3,4-

dihydroxyphenylethanol

(DOPET)

DORAL (quazepam), 466t

Dorzolamide, 680

for ophthalmic use, 1787

Dosage regimens

design and optimization of, 34–37

individualization, 37, 1808

intermittent, interval for, 36

loading, 36–37

maintenance, 35–36

median effective, 73, 74f

median lethal, 73, 74f

Dose

calculation, in prescription writing,

1881

loading, 36–37

of neuromuscular blocking agents,

265t

Dose-dependent reactions, 75–76

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