EFFECTS OF CLONIDINE AND DIAZEPAM ON THE ACOUSTIC STARTLE RESPONSE AND ON ITS INHIBITION BY PREPULSES IN MAN

Citation
Kaj. Abduljawad et al., EFFECTS OF CLONIDINE AND DIAZEPAM ON THE ACOUSTIC STARTLE RESPONSE AND ON ITS INHIBITION BY PREPULSES IN MAN, J PSYCHOPH, 11(1), 1997, pp. 29-34
Citations number
35
Categorie Soggetti
Pharmacology & Pharmacy",Neurosciences,"Clinical Neurology
Journal title
JOURNAL OF PSYCHOPHARMACOLOGY
ISSN journal
02698811 → ACNP
Volume
11
Issue
1
Year of publication
1997
Pages
29 - 34
Database
ISI
SICI code
0269-8811(1997)11:1<29:EOCADO>2.0.ZU;2-D
Abstract
This experiment examined the effects of two sedative/anxiolytic drugs, diazepam and clonidine, on the eyeblink component of the acoustic sta rtle response in healthy volunteers. Twelve males (18-30 years), scree ned for normal hearing thresholds, participated in three sessions in w hich they received oral doses of placebo, diazepam 10 mg and clonidine 200 mu g according to a balanced double-blind protocol. Thirty-minute electromyographic recordings from the orbicularis oculi muscle of the right eye were carried out 120 min after ingestion of clonidine and 6 0 min after ingestion of diazepam. Subjects received 36 40-msec sound pulses (115 dB), separated by variable intervals (mean 25 sec); in 24 of the trials the pulse was preceded by a 40-msec prepulse (75 dB in 1 2 trials and 85 dB in 12 trials; prepulse-pulse interval, 120 msec). T he amplitude of the startle response was significantly reduced both by diazepam (mean +/- SEM: -43.9 +/- 7.4%)and by clonidine (-75.7 +/- 4. 7%). Under the placebo condition, the 75 and 85 dB prepulses inhibited the startle response by 38.6 +/- 6.5 and 70.3 +/- 2.9%, respectively. Neither drug significantly altered the degree of prepulse inhibition. Both drugs reduced self-rated alertness; clonidine reduced systolic b lood pressure and salivation. The results confirm the suppressant effe ct of clonidine on the startle response and show a qualitatively simil ar effect of diazepam; the results also demonstrate the insensitivity of prepulse inhibition of the startle response to doses of sedative dr ugs that are sufficient to attenuate the startle response itself.