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Serotonin Receptors in Myocardial Infarction: Friend or Foe? [PDF]
ACS Chem NeurosciBahr FS +3 more
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A bibliometric study of the most-cited research articles and reviews in Naunyn-Schmiedeberg's Archives of Pharmacology (1969-2024). [PDF]
Naunyn Schmiedebergs Arch PharmacolSeifert R, Hassan W.
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Ferroptosis in Parkinson's disease: a review of molecular mechanisms and emerging therapeutic strategies. [PDF]
Front NeurosciWang L, Zhang Y, Guo L.
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Substance Addiction Rehabilitation Drugs. [PDF]
Pharmaceuticals (Basel)Yuan S, Jiang SC, Zhang ZW, Li ZL, Hu J.
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Inhibitory and excitatory conditioned cues associated with alcohol differentially modulate the nucleus accumbens shell: involvement of 5-HT<sub>7</sub> receptors. [PDF]
Front PsychiatryHauser SR +9 more
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Behavioural effects of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) in monkeys
European Journal of Pharmacology, 1990Subcutaneous injections of a 5-HT1A receptor agonist, 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT), in monkeys induced distinct behavioural changes characterized by head weaving, hindlimb extension and upper limb fluttering. The effects were dose-dependent and were similar to the 5-HT syndrome induced in rats by 8-OH-DPAT.
Kuno Sadako
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The effects of WAY-100135 and 8-hydroxy-2-(di-n-propylamino)tetralin on feeding in the rat
European Journal of Pharmacology, 1994We have examined the effects of the selective 5-HT1A receptor antagonist, WAY-100135, on feeding and on 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT)-induced hyperphagia in rats. Given alone, WAY-100135 (1-10 mg/kg s.c.) did not affect the food intake of fasted or satiated rats; however, in free feeding rats, WAY-100135 (3 mg/kg s.c ...
A Fletcher
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European Journal of Pharmacology, 1993
The ability of a series of compounds to mimic the stimulus properties of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) was compared to: (1) the affinity of these compounds for the 5-HT1A receptor; and (2) their efficacy to inhibit forskolin-stimulated adenylate cyclase activity.
Richard A Rabin, J C Winter
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The ability of a series of compounds to mimic the stimulus properties of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) was compared to: (1) the affinity of these compounds for the 5-HT1A receptor; and (2) their efficacy to inhibit forskolin-stimulated adenylate cyclase activity.
Richard A Rabin, J C Winter
exaly +3 more sources
Behavioural Brain Research, 1989
The influence of the centrally active 5-HT1A agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) on the exploration of objects was studied in hamsters, using a radioactographic method. This spatial paradigm allows the study of the behavioural expression of underlying locomotor and cognitive (attentional, mnemonic, representative) mechanisms. The
Marie-Christine Buhot, Louis Segu
exaly +3 more sources
The influence of the centrally active 5-HT1A agonist 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) on the exploration of objects was studied in hamsters, using a radioactographic method. This spatial paradigm allows the study of the behavioural expression of underlying locomotor and cognitive (attentional, mnemonic, representative) mechanisms. The
Marie-Christine Buhot, Louis Segu
exaly +3 more sources