Changes in brain orexin levels in a rat model of depression induced by neonatal administration of clomipramine

• Published in: Journal of psychopharmacology (Oxford) 2008-09, Vol.22 (7), p.784-791
• Main Authors: Feng, P., Vurbic, D., Wu, Z., Hu, Y., Strohl, KP
• Format: Article
• Language: English
• Subjects: Adult and adolescent clinical studies; Animals; Animals, Newborn; Antidepressants; Biological and medical sciences; Brain; Brain Chemistry - drug effects; Clomipramine; Depression; Depression - chemically induced; Depression - metabolism; Depression - psychology; Depression, Mental; Dosage and administration; Drug therapy; Enzyme-Linked Immunosorbent Assay; Hypothalamus - drug effects; Hypothalamus - metabolism; Intracellular Signaling Peptides and Proteins - metabolism; Male; Medical sciences; Mental depression; Mood disorders; Neuropeptides - analysis; Neuropeptides - metabolism; Neuropharmacology; Orexins; Pathology; Pharmacology. Drug treatments; Phenotype; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer; Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease); Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Psychopharmacology; Radioimmunoassay; Rats; Rats, Long-Evans; Rodents; Serotonin agents; Serotonin Uptake Inhibitors; Swimming - psychology
• ISSN: 0269-8811; 1461-7285
• DOI: 10.1177/0269881106082899

Depression is associated with a deficiency of serotonergic neurons that have been found to suppress orexinergic neurons, which in turn activate these neurons in a feedback loop. This evidence suggests that orexins may be involved in the pathology of depression. Long Evans rats were treated with clomipramine (CLI) and saline (SAL) from postnatal days 8 through 21. One set of rats from both groups was sacrificed at 35 days of age for quantification of orexins in multiple brain regions. At 3—4 months of age a second set of rats was tested for immobility in a forced swim procedure, a common test for depressive signs in rats, and a third set was sacrificed for the quantification of orexins. Compared with the control rats, adult rats with neonatal CLI treatment had (1) increased forced swim immobility and (2) increased orexins A and B in the hypothalamus. However, both orexins A and B levels were decreased in multiple brain regions in the juvenile CLI rats compared with same-age controls. We concluded that although orexin levels were decreased in juvenile CLI rats, adult CLI rats with features of depression had significantly higher levels of hypothalamic orexins compared with adult controls. These results imply that orexins are likely to be involved in the pathological regulation of depression.