✦ LIBER ✦

Participation of dopaminergic structures of the rat brain in passive conditioned avoidance responding

✍ Scribed by V. K. Spiridonov

Book ID: 112509743
Publisher: Springer US
Year: 1976
Tongue: English
Weight: 290 KB
Volume: 8
Category: Article
ISSN: 0090-2977
DOI: 10.1007/bf01297757

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Participation of dopaminergic structures

Participation of dopaminergic structures of the rat brain in passive conditioned avoidance responding

✍ V. K. Spiridonov 📂 Article 📅 1977 🏛 Springer US 🌐 English ⚖ 277 KB

The content of NCAM in rat brain structu

The content of NCAM in rat brain structures in conditioned passive avoidance reactions

✍ A. L. Drozdov; I. A. Leshchinskaya; O. S. Koshelev; V. I. Chernaya 📂 Article 📅 1999 🏛 Springer US 🌐 English ⚖ 213 KB

Block of conditioned avoidance respondin

Block of conditioned avoidance responding in the rat by substituted phenylpiperazines

✍ Gregory E. Martin; Robert J. Elgin Jr.; James M. Kesslick; William J. Baldy; Joa 📂 Article 📅 1988 🏛 Elsevier Science 🌐 English ⚖ 467 KB

Role of noradrenergic terminals of the r

Role of noradrenergic terminals of the rat brain in passive-avoidance conditioning

✍ A. F. Nikiforov; G. G. Knyazev 📂 Article 📅 1975 🏛 Springer US 🌐 English ⚖ 185 KB

Metabolism and Receptor Binding of Serot

Metabolism and Receptor Binding of Serotonin in Brain Structures During Performance of a Conditioned Passive Avoidance Response

✍ G. F. Molodtsova 📂 Article 📅 2005 🏛 Springer US 🌐 English ⚖ 171 KB

The effect of the enantiomers of 3-PPP o

The effect of the enantiomers of 3-PPP on conditioned avoidance responding in the rat

✍ David Clark; Arvid Carlsson; Stephan Hjorth; Jörgen Engel; Per Lindberg 📂 Article 📅 1983 🏛 Springer 🌐 English ⚖ 499 KB

The effects of the enantiomers of 3-PPP on the maintenance of conditioned avoidance responding (CAR) were studied. The weak classical dopamine (DA) agonist (+)-3-PPP failed to interfere with CAR at any dose tested (0.8-13.6 mg/kg). Low doses of the drug produced sedation, while high doses produced b