A single dose of S‐ketamine induces long‐term antidepressant effects and decreases oxidative stress in adulthood rats following maternal deprivation. Issue 11 (19th March 2015)
- Record Type:
- Journal Article
- Title:
- A single dose of S‐ketamine induces long‐term antidepressant effects and decreases oxidative stress in adulthood rats following maternal deprivation. Issue 11 (19th March 2015)
- Main Title:
- A single dose of S‐ketamine induces long‐term antidepressant effects and decreases oxidative stress in adulthood rats following maternal deprivation
- Authors:
- Réus, Gislaine Z.
Carlessi, Anelise S.
Titus, Stephanie E.
Abelaira, Helena M.
Ignácio, Zuleide M.
da Luz, Jaine R.
Matias, Beatriz I.
Bruchchen, Livia
Florentino, Drielly
Vieira, Andriele
Petronilho, Fabricia
Quevedo, João - Abstract:
- <abstract abstract-type="main"> <title>ABSTRACT</title> <p>Ketamine, an antagonist of <italic>N</italic>‐methyl‐<sc>d</sc>‐aspartate receptors, has produced rapid antidepressant effects in patients with depression, as well as in animal models. However, the extent and duration of the antidepressant effect over longer periods of time has not been considered. This study evaluated the effects of single dose of ketamine on behavior and oxidative stress, which is related to depression, in the brains of adult rats subjected to maternal deprivation. Deprived and nondeprived Wistar rats were divided into four groups nondeprived + saline; nondeprived + S‐ketamine (15 mg/kg); deprived + saline; deprived + S‐ketamine (15 mg/kg). A single dose of ketamine or saline was administrated during the adult phase, and 14 days later depressive‐like behavior was assessed. In addition, lipid damage, protein damage, and antioxidant enzyme activities were evaluated in the rat brain. Maternal deprivation induces a depressive‐like behavior, as verified by an increase in immobility and anhedonic behavior. However, a single dose of ketamine was able to reverse these alterations, showing long‐term antidepressant effects. The brains of maternally deprived rats had an increase in protein oxidative damage and lipid peroxidation, but administration of a single dose of ketamine reversed this damage. The activities of antioxidant enzymes superoxide dismutase and catalase were reduced in the deprived rat brains.<abstract abstract-type="main"> <title>ABSTRACT</title> <p>Ketamine, an antagonist of <italic>N</italic>‐methyl‐<sc>d</sc>‐aspartate receptors, has produced rapid antidepressant effects in patients with depression, as well as in animal models. However, the extent and duration of the antidepressant effect over longer periods of time has not been considered. This study evaluated the effects of single dose of ketamine on behavior and oxidative stress, which is related to depression, in the brains of adult rats subjected to maternal deprivation. Deprived and nondeprived Wistar rats were divided into four groups nondeprived + saline; nondeprived + S‐ketamine (15 mg/kg); deprived + saline; deprived + S‐ketamine (15 mg/kg). A single dose of ketamine or saline was administrated during the adult phase, and 14 days later depressive‐like behavior was assessed. In addition, lipid damage, protein damage, and antioxidant enzyme activities were evaluated in the rat brain. Maternal deprivation induces a depressive‐like behavior, as verified by an increase in immobility and anhedonic behavior. However, a single dose of ketamine was able to reverse these alterations, showing long‐term antidepressant effects. The brains of maternally deprived rats had an increase in protein oxidative damage and lipid peroxidation, but administration of a single dose of ketamine reversed this damage. The activities of antioxidant enzymes superoxide dismutase and catalase were reduced in the deprived rat brains. However, ketamine was also able to reverse these changes. In conclusion, these findings indicate that a single dose of ketamine is able to induce long‐term antidepressant effects and protect against neural damage caused by oxidative stress in adulthood rats following maternal deprivation. © 2015 Wiley Periodicals, Inc. Develop Neurobiol 75: 1268–1281, 2015</p> </abstract> … (more)
- Is Part Of:
- Developmental neurobiology. Volume 75:Issue 11(2015:Nov.)
- Journal:
- Developmental neurobiology
- Issue:
- Volume 75:Issue 11(2015:Nov.)
- Issue Display:
- Volume 75, Issue 11 (2015)
- Year:
- 2015
- Volume:
- 75
- Issue:
- 11
- Issue Sort Value:
- 2015-0075-0011-0000
- Page Start:
- 1268
- Page End:
- 1281
- Publication Date:
- 2015-03-19
- Subjects:
- Neurobiology -- Periodicals
Neurobiology
Neurobiologie -- Périodiques
Neurobiology
Periodicals
Periodicals
573.838 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1932-846X ↗
http://www.interscience.wiley.com ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/114030483 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/dneu.22283 ↗
- Languages:
- English
- ISSNs:
- 1932-8451
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3579.057150
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4168.xml