Long-term effects of nicotine on the forced swimming test in mice: An experimental model for the study of depression caused by smoke

• Published in: Neurochemistry international 2006-10, Vol.49 (5), p.481-486
• Main Authors: Mannucci, Carmen, Tedesco, Michele, Bellomo, Maria, Caputi, Achille P., Calapai, Gioacchino
• Format: Article
• Language: English
• Subjects: Animals; Biological and medical sciences; Blotting, Western; Depression; Depression - etiology; Depression - physiopathology; Fundamental and applied biological sciences. Psychology; Male; Mice; Nicotine; Nicotine - administration & dosage; Nicotine - adverse effects; Nicotine - pharmacology; Piperazines - administration & dosage; Pyridines - administration & dosage; Receptor, Serotonin, 5-HT1A - metabolism; Serotonin; Serotonin - administration & dosage; Serotonin - analysis; Serotonin Uptake Inhibitors - pharmacology; Smoke - adverse effects; Smoking; Stress, Physiological - physiopathology; Substance Withdrawal Syndrome; Swimming; Vertebrates: nervous system and sense organs
• ISSN: 0197-0186; 1872-9754
• DOI: 10.1016/j.neuint.2006.03.010

Large evidence showing an association between depression and tobacco smoking is known. Nicotine is the active chemical responsible for smoking addiction, and its withdrawal may induce in smokers greater sensitivity to stress. Our aim has been to investigate the links between tobacco addiction and depression by studying the long-term effects of repeated administration of nicotine followed by dependence, to forced swimming test, serotonin content and 5-HT 1A expression in diencephalon. Dependence has been induced by daily subcutaneous injection in mice of nicotine (2 mg/kg four injections daily) for 15 days and assessed after nicotine withdrawal with an abstinence scale; control animals received daily subcutaneous injection of saline for the same period. Experiments on forced swimming test have been carried out at t = 0 (last day of nicotine or saline treatment), and 15, 30, 45 and 60 days after saline or nicotine withdrawal. Both control mice and nicotine mice have been pre-treated with oral 5-hydroxy-tryptophan (12.5–50 mg/kg), precursor of serotonin, before forced swimming test. Nicotine mice have shown on forced swimming test a significant increase of immobility time compared to control mice. This increase was not evident in nicotine mice treated with 5-hydroxy-tryptophan and treatment with the selective serotonin receptorial antagonist WAY 100635 (WAY) abolished 5-hydroxy-tryptophan effects. Evaluation of diencephalic serotonin, performed at t = 0 showed an increase of diencephalic serotonin content, while serotonin measured 15, 30, 45 and 60 days after nicotine withdrawal, was significantly reduced in nicotine mice compared to control mice. Western blot analysis showed a great reduction of 5-HT 1A receptor expression in nicotine mice measured at t = 0 (last day of treatment) and at 15 and 30 days after nicotine withdrawal compared to control mice. Our results show that (i) behavioural alterations estimated with forced swimming test and (ii) changes in diencephalic serotonin content and 5-HT 1A receptor expression, are present since nicotine is withdrawn even after a long time, suggesting a role of serotonin in mood disorders eventually occurring following smoking cessation.