The tail suspension test as a model for assessing antidepressant activity: review of pharmacological and genetic studies in mice

JF Cryan, C Mombereau, A Vassout - Neuroscience & Biobehavioral …, 2005 - Elsevier
Since its introduction almost 20 years ago, the tail suspension test has become one of the
most widely used models for assessing antidepressant-like activity in mice. The test is based …

Anxiolytic-like effects of the prototypical metabotropic glutamate receptor 5 antagonist 2-methyl-6-(phenylethynyl) pyridine in rodents

WPJM Spooren, A Vassout, HC Neijt, R Kuhn… - … of Pharmacology and …, 2000 - ASPET
Recently, selective and systemically active antagonists for the metabotropic glutamate 5
receptor (mGlu 5 ) were discovered, and the most potent derivative was found to be MPEP (2-…

The selective nicotinic acetylcholine receptor α7 agonist JN403 is active in animal models of cognition, sensory gating, epilepsy and pain

D Feuerbach, K Lingenhoehl, HR Olpe, A Vassout… - …, 2009 - Elsevier
Several lines of evidence suggest that the nicotinic acetylcholine receptor α7 (nAChR α7) is
involved in central nervous system disorders like schizophrenia and Alzheimer's disease as …

The NK1-receptor antagonist NKP608 has an antidepressant-like effect in the chronic mild stress model of depression in rats

M Papp, A Vassout, C Gentsch - Behavioural brain research, 2000 - Elsevier
The chronic mild stress (CMS) model of depression was used to study the potential
antidepressant-like activity of NKP608, a non-peptidic, specific, potent and orally active NK1 receptor …

NKP608: a selective NK-1 receptor antagonist with anxiolytic-like effects in the social interaction and social exploration test in rats

A Vassout, S Veenstra, K Hauser, S Ofner, F Brugger… - Regulatory peptides, 2000 - Elsevier
NKP608 is a non-peptidic derivative of 4-aminopiperidine which acts as a selective, specific
and potent antagonist at the neurokinin-1 (NK-1) receptor both in vitro and in vivo. In vitro, …

Modulation of dopamine-mediated behavioural responses by antidepressants: effects of single and repeated treatment

A Delini-Stula, A Vassout - European journal of pharmacology, 1979 - Elsevier
The study concerned the effects of maprotiline, imipramine, clomipramine and amitriptyline
on the stereotype and turning behaviour induced by apomorphine in rats. At either single or …

Anxiolytic effect of NKP608, a NK1-receptor antagonist, in the social investigation test in gerbils

C Gentsch, M Cutler, A Vassout, S Veenstra… - Behavioural brain …, 2002 - Elsevier
NKP608 is a potent, selective and orally active non-peptidic neurokinin-1 (NK1)-receptor
antagonist for which anxiolytic- and antidepressant-like effects have been described in various …

SAR of 2-benzyl-4-aminopiperidines: CGP 49823, an orally and centrally active non-peptide NK1 antagonist

S Ofner, K Hauser, W Schilling, A Vassout… - Bioorganic & Medicinal …, 1996 - Elsevier
… Silvio Ofner*, Kathleen Hauser, Walter Schilling, Annick Vassout, Siem J. Veenstra … (a)
Vassout, A.; Schanb, M.; Hauser, K.; Schilling, W. "Substance P induces hindlimb thumping …

Differences in pre-and post-synaptic sensitivity to apomorphine between saline and 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine-treated C57BL/6 mice as reflected …

WPJM Spooren, A Vassout, P Waldmeier… - European journal of …, 1998 - Elsevier
The climbing behaviour after low doses (0.05, 0.1 and 0.2 mg/kg) or a high dose (1.5 mg/kg)
of apomorphine was studied in saline or 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (…

Affinity changes of rat striatal dopamine receptors in vivo after acute bupropion treatment

S Bischoff, H Bittiger, J Krauss, A Vassout… - European journal of …, 1984 - Elsevier
The effect of bupropion (Wellbutrin ® ) was studied on in vivo [ 3 H]spiperone binding in rat
striatum and cerebellum. The compound increased binding dose dependently in striatum …