Documents about Pharmacology in general. Not for documents on specific substances. For broad ranged documents, first check out if it fits in the categories: 'Hallucinogens', 'downers', 'dissociatives' or 'stimulants'.
Abstract: A homology-based model of the 5-HT2A receptor was produced utilizing an activated form of the bovine rhodopsin (Rh) crystal structure [1,2]. In silico activation of the Rh structure was accomplished by isomerization of the 11-cis-retinal (1) chromophore, followed by constrained molecular...
Submitted by Metomni
16-04-2008
323.21 Kbytes
Hits 33
Published 1917 by Saunders.
Downloadable PDF (41.3 MB) hosted on Google Books.
Interesting from a historical perspective (includes things such as cannabis, cocaine, opiates, hops, etc).
If the file doesn't open, try http://books.google.com/books?id=l1AQ9w_iFMoC&printsec=frontcover
You can...
Submitted by Paracelsus
28-01-2008
1.43 Kbytes
Hits 170
From the Brithish Journal of Psychiatry 1989 - Barnes Akathisia Scale. Akathisia is a state of "inner restlessness" and can be caused by a range of drugs, notably anti psychotics, SSRI and tricyclic antidepressants, antihistamines and anti-emetic drugs.
Cowen PJ & Nutt DJ. (1982). Abstinence symptoms after withdrawal from tranquillising drugs; is there a common neurochemical mechanism? Lancet, 2: 360-2.
Abstract: Withdrawal of anxiolytic agents such as ethanol, barbiturates, and benzodiazepines may result in a syndrome characterised in its most...
Modulation of glutamatergic neurotransmission by metabotropic glutamate2/3 (mGlu2/3) receptor agonists effectively treats seemingly diverse neuropsychiatric illness such as generalized anxiety disorder and schizophrenia. Activation of adenosine A1 heteroceptors, like mGlu2...
Submitted by Gradient
07-08-2009
157.44 Kbytes
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The dopamine hypothesis of drug reward remains a difficult area of research and perhaps a major problem and hindrance to progress in unraveling the biology of addiction. Pharmacological treat-ment of drug dependency has been disappointing and new therapeutic targets and hypotheses are needed. Since...
Natalie D. Stull, David P. Polan and Lorraine Iacovitti
Using tissue culture models of oxidative stress caused by serum deprivation or MPTP/MPP+ toxicity, the present study establishes that the antioxidants epigallocatechin gallate, lazaroids U74389G and U83836E, reservatrol, MnTBAP, MCI 186,...
Submitted by Gradient
11-08-2009
1.52 Mbytes
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Originally published in Psychosomatics
Looks at the interactions of HIV drugs with various drugs, including alcohol, benzodiazepines, cocaine, GHB, ketamine, LSD, MDMA, opiates, PCP and marijuana
Clinical Pharmacology and Therapeutics 2008 Apr;83(4):622-6
Schoedel KA, Sellers EM
As public health concerns have changed, regulatory expectations for assessing abuse liability of new central nervous system (CNS) drugs have increased. All CNS-active drugs with any properties indicating...
Submitted by Jatelka
12-04-2008
120.86 Kbytes
Hits 29
Keywords: abuse
Allan AM, Zhang X, & Baier LD. (1992). Barbiturate tolerance: effects on GABA-operated chloride channel function. Brain Research, 588(2):255-60.
Abstract: Male ICR mice were fed powdered laboratory chow containing phenobarbital for 7 days to induce tolerance. Mice were sacrificed and brains...
Abstract: -Carboline alkaloids are a large group of natural and synthetic indole alkaloids with different degrees of aromaticity,
some of which are widely distributed in nature, including various plants, foodstuffs, marine creatures, insects,
mammalians as...
Submitted by Quantum Dude
11-01-2009
494.10 Kbytes
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Submitted by Heretic.Ape.
07-05-2007
56.90 Kbytes
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From JPPS 1(1), 1998
Submitted by Heretic.Ape.
12-05-2007
331.25 Kbytes
Hits 105
Keywords: buccal
Goldfish cones contain CB1 receptors at the synaptic terminal, selectively accumulate 3H-anandamide, and contain fatty acid amide hydrolase-immunoreactivity, and voltage-gated calcium and potassium currents are modulated by CB1 ligands (Yazulla et al., 2000; Fan & Yazulla, 2003; Glaser et al.,...
The analgesic effect of opioids is enhanced, and tolerance is attenuated, by ultra-low doses (nanomolar to picomolar) of an opioid antagonist, an effect that is mediated by preventing the receptor from coupling to Gs proteins. Recently, we demonstrated a cannabinoid-opioid interaction at the...
The efficacy of individual antihistamines is similar for most indications. The primary difference between traditional (first-generation) and nonsedating (second-generation) histamine1-receptor antagonists is the incidence and severity of adverse reactions. The first-generation drugs are associated...
Submitted by Gradient
08-07-2009
1.34 Mbytes
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Abstract: Substance abuse and addiction are the most costly of all the neuropsychiatric disorders. In the last decades, much progress has been achieved in understanding the effects of the drugs of abuse in the brain. However, efficient treatments that prevent relapse have not been developed. Drug...
Submitted by Gradient
19-07-2009
569.08 Kbytes
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Some patients with difficult-to-treat epilepsy benefit from combination therapy with two or more antiepileptic drugs (AEDs). Additionally, virtually all epilepsy patients will receive, at some time in their lives, other medications for the management of associated conditions. In these situations,...
Feinberg SS. Journal of Clinical Psychiatry 2004 Nov;65(11):1520-4.
BACKGROUND: Among antidepressant augmentation strategies, the addition of a stimulant to a monoamine oxidase inhibitor (MAOI) has received little attention in the literature in recent years because of the diminished clinical use...
Submitted by Metomni
02-04-2008
47.53 Kbytes
Hits 67
Baker LE, Panos JJ, Killinger BA, Peet MM, Bell LM, Haliw LA, Walker SL. (2009). Comparison of the discriminative stimulus effects of salvinorin A and its derivatives to U69,593 and U50,488 in rats. Psychopharmacology, 203(2): 203-211.
Abstract: This study compared the discriminative stimulus...
This paper details the isolation of serotonin (5-HT) from bovine serum.
Submitted by Synchronium
12-04-2009
507.32 Kbytes
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Three series of cycloalkanecarboxylic esters derived from the naturally occurring clavine
alkaloids lysergol, dihydrolysergol-I, and elymoclavine were synthesized to study their
interaction with 5-HT2A receptors and R1-adrenoceptors in rat tail artery and aorta, respectively.
Especially...
Submitted by trptamene
10-11-2007
193.73 Kbytes
Hits 31
Interesting deconstruction of Red Bulls claims about taurine's role in it's product's "cognitive & muscular enhancement".
Submitted by Micklemouse
28-12-2007
109.42 Kbytes
Hits 107
Journal of Clinical Psychopharmacology 2002 Jun;22(3):330-2.
Authors: David Pritzker, Anish Kanungo, Tansel Kilicarslan, Rachel F. Tyndale and Edward M. Sellers
To explore the hydrophobic groove subsite within the CB1 cannabinoid receptor we have designed and
synthesized a group of tail-substituted anandamide analogs. Our design involves the introduction of aryl
or heterocyclic ring as terminal substituents that are connected to the last...
Submitted by helikophis
17-05-2009
355.82 Kbytes
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Jianfei Chaoa, b, Man-Shan Yub, Yuen-Shan Hob, c, Mingfu Wanga, , and Raymond Chuen-Chung Chang
Oxyresveratrol (OXY) is a polyhydroxylated stilbene existing in mulberry. Increasing lines of evidence have shown its neuroprotective effects against Alzheimer disease and stroke. However, little is...
Submitted by Gradient
11-08-2009
1.14 Mbytes
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Originally published in The Heffter Review of Psychedelic Research.
[Dopamine supersensitivity occurs in schizophrenia and other psychoses, and after hippocampal lesions, antipsychotics, ethanol, amphetamine, phencyclidine, gene knockouts involving dopamine receptors and enzymes that function in dopamine-containing neurons.
The functional state of D2, or the...
Submitted by Ilsa
26-02-2009
748.04 Kbytes
Hits 18
Originally published in The Mayo Clinic Proceedings.
Covers much of the same material as the other review article
Lanteri C, Salomon L, Torrens Y, Glowinski J, Tassin JP
A challenge in drug dependence is to delineate long-term neurochemical modifications induced by drugs of abuse. Repeated d-amphetamine was recently shown to disrupt a mutual regulatory...
Submitted by Jatelka
13-04-2008
223.49 Kbytes
Hits 18
Submitted by Alfa
08-12-2006
102.77 Kbytes
Hits 79
Andersson T, Cederberg C, Edvardsson G, Heggelund A, & Lundborg P. (1990). Effect of omeprazole treatment on diazepam plasma levels in slow versus normal rapid metabolizers of omeprazole. Clinical Pharmacology & Therapeutics, 47(1):79-85.
Abstract: The effect of omeprazole treatment on diazepam...
Submitted by Heretic.Ape.
12-05-2007
116.73 Kbytes
Hits 51
Psychopharmacology 1991;104(1):27-34.
Sanger DJ, Joly D.
Recent studies have shown that several compounds known to act as competitive or non-competitive antagonists of NMDA receptors can disrupt learning in rodents. The present study was carried out to investigate the effects of a range of...
Consumption of typical quantities of grapefruit juice (GFJ) increases the oral bioavailability of several CYP3A4 substrates without affecting their elimination, consistent with selective inhibition of intestinal but not hepatic CYP3A4. However, increases in the AUCs of CYP3A4 substrates recently...