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  • Valproic acid also blocks the [[voltage-gated sodium channel]]s and T-type calcium channels. These mechanisms make valproic acid a broad spectrum anticonvulsa Valproate is a known folate antagonist, which can cause [[neural tube defects]]. Thus, folic acid supplements may
    25 KB (3,328 words) - 16:47, 27 September 2010
  • ...ertensive]] and in the treatment of [[Angina pectoris|angina]]. Like other calcium channel blockers, amlodipine acts by relaxing the [[smooth muscle]] in the ...ine is an ionized compound (pKa=8.6), and its kinetic interaction with the calcium channel receptor is characterized by a gradual rate of association and diss
    12 KB (1,641 words) - 15:32, 16 September 2010
  • ...elective [[beta-1 receptor|β<sub>1</sub> receptor]] [[receptor_antagonist|antagonist]], a [[drug]] belonging to the group of [[beta blockers]] (sometimes writte ...f additional negative impact on the muscular strength of the heart. Use of calcium-antagonists of the [[nifedipine]]-type is controversial..
    12 KB (1,720 words) - 16:48, 27 September 2010
  • ...journal |author=Korpi ER, Kuner T, Seeburg PH, Lüddens H |title=Selective antagonist for the cerebellar granule cell-specific gamma-aminobutyric acid type A rec ...ration]] and [[electrolyte imbalance]], including loss of [[potassium]], [[calcium]], [[sodium]], and [[magnesium]]. It is especially important to prevent pot
    12 KB (1,678 words) - 16:48, 27 September 2010
  • * Duration of action prolonger in states of low potassium, calcium and protein, also in states of high magnesium and acidosis.
    3 KB (457 words) - 16:48, 27 September 2010
  • ...[[secretion]]. It is a non-selective [[muscarinic]] [[Receptor antagonist|antagonist]], and does not diffuse into the blood, which prevents systemic side-effect
    5 KB (580 words) - 16:49, 27 September 2010
  • ...calcium uptake in cortisol-treated chickens: evidence for dissociation of calcium absorption from brush border vesicle uptake |journal=Proc. Natl. Acad. Sci. ...ng target cells.<ref>Davies E. Keyon, C.J.; Fraser, R. (1985) "The role of calcium ions in the mechanism of ACTH stimulation of cortisol synthesis." Steroids
    41 KB (5,644 words) - 16:50, 27 September 2010
  • ...ate some counter-regulatory pathways responsible for opioid tolerance. CCK-antagonist drugs, specifically [[proglumide]], have been shown to slow the development ..., and [[methadone]] and its derivatives; all of these drugs also have NMDA antagonist properties. It is believed that the strong opioid with the most incomplete
    87 KB (12,376 words) - 16:51, 27 September 2010
  • ..._agents|class IV]]<br/>([[Cardiac_action_potential#Phase_4|Phase 4]]→, [[calcium channel blocker|Ca<sup>2+</sup> channel blockers]]) ...ceptor (biochemistry)|Receptor]] [[agonist]]s<BR>and [[Receptor antagonist|antagonist]]s
    3 KB (298 words) - 12:09, 19 September 2010
  • ''[[histamine antagonist]]s'' ([[Levocabastine]], [[Antazoline]], [[Thonzylamine]]) | list4 = [[Cafaminol]]{{•}} [[Calcium hexamine thiocyanate]]{{•}} [[Retinol]]{{•}} [[Ipratropium|Ipratropium
    2 KB (149 words) - 15:10, 6 July 2010
  • | group2 = [[Receptor antagonist|Receptor antagonist]]s and/or [[Reuptake inhibitor|reuptake inhibitor]]s | group1 = <small>[[Serotonin antagonist and reuptake inhibitor|Serotonin antagonists and reuptake inhibitor]]s (SAR
    13 KB (1,038 words) - 16:53, 27 September 2010
  • ...cylic acid/Aspirin]]<sup>#</sup>{{•}} [[Aloxiprin]]{{•}} [[Carbasalate calcium]]{{•}} [[Indobufen]]{{•}} [[Triflusal]] ...ole]], [[Picotamide]]){{•}} ''[[Thromboxane receptor antagonist|receptor antagonist]]'' ([[Terutroban]]<sup>†</sup>)
    4 KB (372 words) - 16:54, 27 September 2010
  • ...]{{·}} [[Methylcellulose]]{{·}} [[Wheat|Triticum]]{{·}} [[Polycarbophil calcium]] | group6 = Peripheral [[opioid antagonist]]s
    2 KB (134 words) - 16:53, 27 September 2010
  • |group2 = [[Endothelin receptor antagonist]]s |list5 = [[Calcium channel blocker]]s, [[Diuretic]]s, [[Digoxin]], [[Oxygen therapy]], [[Warfa
    808 bytes (84 words) - 12:10, 19 September 2010
  • | list1 = ''stomach acid'' ([[Antacid]]s, [[H2 antagonist|H<sub>2</sub> antagonist]]s, [[Proton pump inhibitor]]s){{•}} [[Antiemetic]]s{{•}} [[Laxative]]s ...enin-angiotensin system]]'' ([[ACE inhibitor]]s, [[Angiotensin II receptor antagonist]]s, [[Renin inhibitor]]s)
    5 KB (556 words) - 19:23, 27 September 2011
  • ...[[Distal convoluted tubule|DCT]],<BR>[[Diuretic#Calcium-sparing_diuretics|Calcium-sparing]]) | group2 = [[Aldosterone antagonist]]s
    3 KB (239 words) - 12:10, 19 September 2010
  • ...try)|Receptor]]: [[Receptor agonist|Agonist]]{{•}} [[Receptor antagonist|Antagonist]]{{•}} [[Positive allosteric modulator]] (PAM){{•}} [[Negative alloster | list2 = [[Calcium channel blocker]] (CCB){{•}} [[Potassium channel blocker]] (PCB){{•}} [
    4 KB (375 words) - 12:11, 19 September 2010
  • ...tabotropic glutamate receptor|mGluR]]'' ([[Acamprosate]]){{·}} ''[[opioid antagonist|Opioid receptor antagonists]]'' ([[Naltrexone]], [[Nalmefene]]){{·}} [[Top
    3 KB (233 words) - 12:11, 19 September 2010
  • | group2 = [[Oxytocin]] antagonist | group4 = [[Calcium channel blocker]]
    763 bytes (74 words) - 12:11, 19 September 2010
  • | list1 = [[Ammonium chloride]]{{·}} [[Calcium chloride]] | group2 = [[Urinary]] [[antispasmodic]]s<BR>(primarily [[Muscarinic antagonist|antimuscarinics]])
    2 KB (155 words) - 12:11, 19 September 2010

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