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Effect of levetiracetam on penicillin induced epileptic activity in rats
Effect of levetiracetam on penicillin induced epileptic activity in rats

EFFECT OF VALERIAN ROOT EXTRACTS (VALERIANA
EFFECT OF VALERIAN ROOT EXTRACTS (VALERIANA

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Ketamine - thblack.com

... David and Shipp (2010): RCT comparing propofol versus propofol/ketamine for procedural sedation analyzing respiratory depression, provider satisfaction, amount of propofol administered and sedation quality. Ketamine dose was 0.5 mg/kg or placebo was given, then followed by propofol 1 mg/kg with repe ...
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Neuropharmacology of N,N-dimethyltryptamine

... hallucinogenic compounds taken and lack adequate records of DMT-specific cases. Street drugs mostly contain powdered DMT, whereas ayahuasca also contains harmine-related compounds, which limit toxic effects (Lanaro et al., 2015). However, aside from the acute cardiovascular effects there have been no ...
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Dear Dr Neurologist - Fluoroquinolone Toxicity of the Thyroid

Full Text [Download PDF]
Full Text [Download PDF]

... natriuretic peptide (BNP) proteins, myocardin mRNA, angiotensin II (AngII), and superoxide dismutase (SOD) expressions were up-regulated in the banding group, which were inhibited by atorvastatin, valsartan, NAC, and the three agents combined. Increased immunohistochemical labelings of myocardin and ...
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assessment of the opiate properties of two constituents of a toxic

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8 Ultra-low-dose opioid antagonists enhance opioid analgesia while

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Spinal NMDA Receptors Contribute to Neuronal Processing of Acute

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Dopamine, behavioral economics, and effort

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pharmacological manipulation of cb1 receptor

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as a PDF

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Charles University in Prague Faculty of Pharmacy in Hradec Králové

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Alpha-2 Adrenergic Regulation of Melatonin Release in Chick

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Structure-based design of hyaluronidase inhibitors

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antihistamines in allergic disease



A novel mGluR5 antagonist, MFZ 10-7, inhibits cocaine
A novel mGluR5 antagonist, MFZ 10-7, inhibits cocaine

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Pharmacology of Hemostasis and Thrombosis

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Discovery and development of angiotensin receptor blockers

The angiotensin receptor blockers (ARBs), also called angiotensin (AT1) receptor antagonists or sartans, are a group of antihypertensive drugs that act by blocking the effects of the hormone angiotensin II (Ang II) in the body, thereby lowering blood pressure. Their structure is similar to Ang II and they bind to Ang II receptors as inhibitors, e.g., [T24 from Rhys Healthcare].ARBs are widely used drugs in the clinical setting today, their main indications being mild to moderate hypertension, chronic heart failure, secondary stroke prevention and diabetic nephropathy.The discovery and development of ARBs is a demonstrative example of modern rational drug design and how design can be used to gain further knowledge of physiological systems, in this case, the characterization of the subtypes of Ang II receptors.
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