Mice given one-triM passive avoidance training were examined 24 hours later for retention of the acquired response. Testing was carried out with subjects given either ehlorpromazine or saline injections before the test session. Three chlorpromazine doses (0.5, 2.0, and 3.5 mg]kg) were used, and thre
An analysis of chlorpromazine-induced suppression of the avoidance response
β Scribed by Donald Posluns
- Publisher
- Springer
- Year
- 1962
- Tongue
- English
- Weight
- 807 KB
- Volume
- 3
- Category
- Article
- ISSN
- 0033-3158
No coin nor oath required. For personal study only.
β¦ Synopsis
Chlorpromazine, one of the phenothiazine derivatives, suppresses the avoidance response at doses which neither produce ataxia nor impair the performance of an escape response (Cook et al. ; MILLn~ et M., 1957 a; MAF~II). The avoidance response suppression is a property of most, if not all, phenothiazine derivatives (FE~,LOWS & COOK; InvI~; STONE; COOK & KELL~ER), and can be manifested during acquisition and extinction (ADEn & CLINK; MILLEn et al., 1957a MILLEn et al., , 1957b)), as well as maintenanee, of the response (COOK & W~ID~Eu VER~AVE et al.). The avoidance-suppressing property of the phenothiazine derivatives may be related to the drugs' action in relieving psychotic disorders, because a rank order relation has been demonstrated between the dose at which any one phenothiazine derivative suppresses the avoidance response and its rglative potency in psychotic relief (Cook & KELLn~ER). However, some nonataraetic compounds, including morphine and belladonna alkaloids such as atropine and scopolamine, also specifically suppress the avoidance response (MI~Lso~ et M. cited by BEROEn; MAFFII; PASKAL & VA~DnnWOLF). A more detailed discussion can be found in HEnz's review of drug-induced avoidance response suppression.
The three experiments reported here form part of a systematic search for the factors underlying the specific suppression of the avoidance response by chlorpromazine. Two separate conclusions have been reached to explain chlorpromazine-indueed avoidance response suppression. Some investigators (e.g., ADEn & CLI~K; MILL~n et al., 1957a; Ton~Es) have suggested that chlorpromazine reduces "fear" or "anxiety" the presence of which is believed necessary ~or the reinforcement of the avoidance response. The "fear reduction" suggestion has an intuitive plausibility to it because of the drug's therapeutic effect, but other investigators (e.g., KILLA~ & KILLA~; BnA~)LEY; Knu have concluded that ehlorpromazine produces an impairment of "sensory-arousal" functions, an impairment which could suppress the avoidance response by inhibiting
π SIMILAR VOLUMES
It has been demonstrated that 3,4-dihydroxyphenylalanine (DOPA) can temporarily counteract the reserpine-induced suppression of motor activity (CA~LSSO~ et al. 1957; BLASCttKO and CRVSCIEL 1960; SMITE and DEWS 1962). Both BEnTLE~ and I~OSENG~E~ (1959a), and EVERETT and WIEGAND (1962) have demonstrat
A single injection of reserpine causes depletion of 5-hydroxytryptamine and the catechol amines in brain and other tissues where these amines occur (SHowy., SILVEr, and BI~ODIE 1955, CARLSSO~ et al. 1957 a) and causes sedation and ptosis as well as other disturbances of the autonomic nervous system.