Neurobehavioural Effects of Acute and Repeated Administrations of Sub-Psychotomimetic Dose of Ketamine in Mice
Soliu Abiola Atunwa, Oluwole Isaac Adeyemi, Adegboyega Rotimi Owolabi
Abstract
Soliu Abiola Atunwa, Oluwole Isaac Adeyemi, Adegboyega Rotimi Owolabi
Abstract
Recent studies have shown that sub-anaesthetic doses of ketamine may induce analgesia, but its psychotomimetic side effects have called for caution. This study therefore, explored a possible sub-psychotomimetic dose of ketamine (SPDK) and determined the influence of frequency of exposure on its neurobehavioural effects in mice. Mice of either sex weighing 18 - 25 g were randomly selected into three major groups: A, B, and C. Group A was distributed into seven sub-groups (n=12) and treated with saline (10 μL/g/body weight); 1, 2, 4, 6, 8, and 10 mg/kg ketamine for stereotyped horizontal locomotion (SHL) assessment using the open field test. Groups B and C were each allotted into three sub-groups (n=7): I, II, and III. They were treated with saline (10 μL/g/body weight) as negative control, 1 mg/kg ketamine and 1.5 mg/kg scopolamine as positive control; and assessed for neurobehavioural effects of acute and repeated administrations using elevated plus-maze (EPM) and Y-maze respectively. Data were presented as Mean ± SEM and analyzed using ANOVA followed by Student-Newman-Keuls test with p 0.05), whereas, ketamine 2, 4, 6, 8 and 10 mg/kg induced significant increase (8.258, p 0.8654) and Y-maze models (1.258, p > 0.3126). This study concluded that 1 mg/kg of ketamine may be a sub-psychotomimetic dose; and ketamine-induced psychotomimetic side effects and cognitive impairments could be dose and time-dependent respectively
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Recent studies have shown that sub-anaesthetic doses of ketamine may induce analgesia, but its psychotomimetic side effects have called for caution. This study therefore, explored a possible sub-psychotomimetic dose of ketamine (SPDK) and determined the influence of frequency of exposure on its neurobehavioural effects in mice. Mice of either sex weighing 18 - 25 g were randomly selected into three major groups: A, B, and C. Group A was distributed into seven sub-groups (n=12) and treated with saline (10 μL/g/body weight); 1, 2, 4, 6, 8, and 10 mg/kg ketamine for stereotyped horizontal locomotion (SHL) assessment using the open field test. Groups B and C were each allotted into three sub-groups (n=7): I, II, and III. They were treated with saline (10 μL/g/body weight) as negative control, 1 mg/kg ketamine and 1.5 mg/kg scopolamine as positive control; and assessed for neurobehavioural effects of acute and repeated administrations using elevated plus-maze (EPM) and Y-maze respectively. Data were presented as Mean ± SEM and analyzed using ANOVA followed by Student-Newman-Keuls test with p 0.05), whereas, ketamine 2, 4, 6, 8 and 10 mg/kg induced significant increase (8.258, p 0.8654) and Y-maze models (1.258, p > 0.3126). This study concluded that 1 mg/kg of ketamine may be a sub-psychotomimetic dose; and ketamine-induced psychotomimetic side effects and cognitive impairments could be dose and time-dependent respectively
Key concepts: Psychotomimetic, Ketamine, Saline, Anesthesia, Analysis of variance, Medicine, Pharmacology, NMDA receptor