The effect of recording interval lenght on behavioral assessment using the forced swimming test
- Álvarez-Suárez, Paloma 1
- Banqueri, María 1
- Vilella, Marina 1
- Méndez López, Marta 1
- Arias Pérez, Jorge Luis 1
-
1
Universidad de Oviedo
info
ISSN: 2171-2069
Datum der Publikation: 2015
Ausgabe: 6
Nummer: 2
Seiten: 90-95
Art: Artikel
Andere Publikationen in: Revista iberoamericana de psicología y salud
Zusammenfassung
El test de natación forzada es un método utilizado para evaluar el comportamiento depresivo en roedores. Las modificaciones del procedimiento del test de natación forzada desarrollado por Porsolt y su influencia en sus resultados es un tema que suscita controversia y ha sido analizado en numerosos estudios. El comportamiento del animal se analiza generalmente mediante el registro de intervalos parciales, dividiendo el tiempo total de grabación en intervalos iguales y registrando manualmente la conducta predominante durante ese tiempo. A pesar de la influencia del método de registro en los resultados posteriores, esta cuestión no se ha analizado ni normalizado. El objetivo de este estudio fue comprobar si la representatividad de los datos se ve afectada por la longitud del intervalo de observación, registrando a 3, 5 y 10 seg la conducta (inmovilidad, natación y escalada) de los mismos sujetos. Se utilizo una muestra no patológica de ratas Wistar macho y hembra adultas. Los resultados mostraron que no existen diferencias significativas entre estos intervalos analizados en la prueba de natación forzada para las 3 principales conductas registradas.
Informationen zur Finanzierung
Geldgeber
- Spanish Ministry of Economy and Competitiveness
Bibliographische Referenzen
- Bai, M., Zhang, L., Zhu, X., Zhang, Y., Zhang, S., & Xue, L. (2014). Comparison of depressive behaviors induced by three stress paradigms in rats. Physiology & Behavior, 131, 81---86.
- Belzung, C., & Lemoine, M. (2011). Criteria of validity for animal models of psychiatric disorders: Focus on anxiety disorders and depression. Biology of Mood & Anxiety Disorders, 1, 9.
- Bogdanova, O. V., Kanekar, S., D’Anci, K. E., & Renshaw, P. F. (2013). Factors influencing behavior in the forced swim test. Physiology & Behavior, 118, 227---239.
- Borsini, F., & Meli, A. (1988). Is the forced swimming test a suitable model for revealing antidepressant activity? Psychopharmacology, 94, 147---160.
- Borsini, F., Volterra, G., & Meli, A. (1986). Does the behavioral despair test measure ‘despair’? Physiology & Behavior, 38, 385---386.
- Briones, A., Gagno, S., Martisova, E., Dobarro, M., Aisa, B., Solas, M., et al. (2012). Stress-induced anhedonia is associated with an increase in Alzheimer’s disease related markers. British Journal of Pharmacology, 165, 897---907.
- Citó, M. C. O., Silva, M. I. G., Santos, L. K. X., Fernandes, M. L., Melo, F. H. C., Aguiar, J. A. C., et al. (2015). Antidepressantlike effect of Hoodia gordonii in a forced swimming test in mice: Evidence for involvement of the monoaminergic system. Brazilian Journal of Medical and Biological Research, 48, 57---64.
- Deak, T., Bellamy, C., D’Agostino, L. G., Rosanoff, M., McElderry, N. K., & Bordner, K. A. (2005). Behavioral responses during the forced swim test are not affected by anti-inflammatory agents or acute illness induced by lipopolysaccharide. Behavioural Brain Research, 160, 125---134.
- El-Alfy, A. T., Ivey, K., Robinson, K., Ahmed, S., Radwan, M., Slade, D., et al. (2010). Antidepressant-like effect of �9- tetrahydrocannabinol and other cannabinoids isolated from Cannabis sativa. Pharmacology Biochemistry and Behaviour, 95, 434---442.
- Fiske, K., & Delmolino, L. (2012). Use of discontinuous methods of data collection in behavioral intervention: Guidelines for practitioners. Behavior Analysis in Practice, 5, 77---81.
- Gersner, R., Gordon-Kiwkowitz, M., & Zangen, A. (2009). Automated behavioral analysis of limbs’ activity in the forced swim test. Journal of Neuroscience Methods, 180, 82---86.
- Grillo, C. A., Piroli, G. G., Kaigler, K. F., Wilson, S. P., Wilson, M. A., & Reagan, L. P. (2011). Downregulation of hypothalamic insulin receptor expression elicits depressive-like behaviors in rats. Behavioural Brain Research, 222, 230---235.
- Harrop, A., & Daniels, M. (1986). Methods of time sampling: A reappraisal of Momentary Time Sampling and Partial Interval Recording. Journal of Applied Behavior Analysis, 19, 73---77.
- Hawkins, J., Hichs, R. A., Phillips, N., & Moore, J. D. (1978). Swimming rats and human depression. Nature, 274---512.
- Hédou, G., Pryce, C., Di lorio, L., Heidbreder, C. A., & Feldon, J. (2001). An automated analysis of rat behavior in the forced swim test. Pharmacology Biochemistry and Behavior, 70, 65---76.
- Holmes, A., Yang, R. J., Murphy, D. L., & Crawley, J. N. (2001). Evaluation of antidepressant-related behavioral responses in mice lacking the serotonin transporter. Neuropsychopharmacology, 27, 914---923.
- Hong, S., Flashner, B., Chiu, M., ver Hoeve, E., Luz, S., & Bhatnagar, S. (2012). Social isolation in adolescence alters behaviors in the forced swim and sucrose preference tests in female but not in male rats. Physiology & Behavior, 105, 269---275.
- Karson, A., Demirtas, T., Bayramgürler, D., Balci, F., & Utkan, T. (2013). Chronis administration of infliximab (TNF-� inhibitor) decreases depression and anxiety-like behavior in rat model of chronic mild stress. Basic & Clinical Pharmacology & Toxicology, 112, 335---340.
- Kawai, H., Ishibashi, T., Kudo, N., Kawashima, Y., & Mitsumoto, A. (2012). Behavioral and biochemical characterization of rats treated chronically with thioacetamide: Proposal of an animal model for hepatic encephalopathy associated with cirrhosis. Journal of Toxicological Sciences, 37, 1165---1175.
- Kołaczkowski, M., Marcinkowska, M., Bucki, A., SÌniecikowska, J., PawÅowski, M., Kazek, G., et al. (2014). Novel 5-HT6 receptor antagonists/D2 receptor partial agonists targeting behavioral and psychological symptoms of dementia. European Journal of Medicinal Chemistry, 92, 221---235.
- Krishnan, V., & Nestler, E. J. (2011). Animal models of depression: Molecular perspectives. Current Topics in Behavioral Neurosciences, 7, 121---147.
- Kuœmider, M., Solich, J., Pasach, P., & Dziedzicka-Wasylewska, M. (2007). Effect of citalopram in the modified forced swim test in rats. Pharmacological Reports, 59, 785---788.
- Landis, J. R., & Koch, G. G. (1977). The measurement of observer agreement for categorical data. Biometrics, 33, 159---174.
- Lucki, I., Dalvi, A., & Mayorga, A. J. (2001). Sensitivity to the effects of pharmacologically selective antidepressants in different strains of mice. Psychopharmacology, 155, 315---322.
- Martínez, A. R., Brunelli, S. A., & Zimmerberg, B. (2015). Communal nesting exerts epigenetic influences on affective and social behaviors in rats selectively bred for an infantile trait. Physiology & Behavior, 139, 97---103.
- McKinney, W. T., & Bunney, W. E. (1969). Animal model of depression: Review of evidence and implications for research. Archives of General Psychiatry, 21, 240---248.
- Papaioannou, A., Gerozissis, K., Prokopiou, A., Bolaris, S., & Stylianopoulou, F. (2002). Sex differences in the effects of neonatal handling on the animal’s response to stress and the vulnerability for depressive behavior. Behavioural Brain Research, 129, 131---139.
- Petit-Demouliere, B., Chenu, F., & Bourin, M. (2005). Forced swimming test in mice: A review of antidepressant activity. Psychopharmacology, 177, 245---255.
- Porsolt, R. D., Bertin, A., & Jalfre, M. (1977). Behavioral despair in mice: A primary screening test for antidepressants. Archives internationales de pharmacodynamie et de thérapie, 229, 327---336.
- Porsolt, R. D., LePichon, M., & Jalfre, M. (1977). Depression: A new animal model sensitive to antidepressant treatments. Nature, 266, 730---732.
- Repp, A. C., Roberts, D. M., Slack, D. J., Repp, C. F., & Berkler, M. S. (1976). A comparison of frequency, interval and time-sampling methods of data collection. Journal of Applied Behavior Analysis, 9, 501---508.
- Shaldubina, A., Einat, H., Bersudsky, Y., & Belmaker, R. H. (2005). Epi-inositol is ineffective in Porsolt Forced Swim Test model of depression. Neuropsychiatric Disease and Treatment, 1, 180---190.
- Sirianni, R. W., Olausson, P., Chiu, A. S., Taylor, J. R., & Saltzman, W. M. (2010). The behavioral and biochemical effects of BDNF containing polymers implanted in the hippocampus of rats. Brain Research, 1321, 40---50.
- Su, J., Hato-Yamada, N., Araki, H., & Yoshimura, H. (2013). A test--retest paradigm of the forced swimming test in female mice is not valid for predicting antidepressant-like activity: Participation of acetylcholine and sigma-1 receptors. Journal of Pharmacological Sciences, 123, 246---255.
- Ulloa, R. E., Díaz-Valderrama, A., Herrera-Pérez, J., León-Olea, M., & Martínez-Mota, L. (2014). Age differences in the impact of forced swimming test on serotonin transporter levels in lateral septum and dorsal raphe. Behavioral and Brain Functions, 10, 1---8.
- Uz, T., Dimitrijevic, N., Imbesi, M., Manev, H., & Manev, R. (2008). Effects of MK-886, a 5-lipoxygenase activating protein (FLAP) inhibitor, and 5-lipoxygenase deficiency on the forced swimming behavior of mice. Neuroscience Letters, 436, 269---272.
- Wirth, O., Slaven, J., & Taylor, M. A. (2014). Interval sampling methods and measurement error: A computer simulation. Journal of Applied Behavior Analysis, 47, 83---100.
- Yang, C., Hu, Y. M., Zhou, Z. Q., Zhang, G. F., & Yang, J. J. (2013). Acute administration of ketamine in rats increases hippocampal BDNF and mTOR levels during forced swimming test. Upsala Journal of Medical Sciences, 118, 3---8.