American Journal of Pharmacological Sciences
ISSN (Print): 2327-6711 ISSN (Online): 2327-672X Website: https://www.sciepub.com/journal/ajps Editor-in-chief: Srinivas NAMMI
Open Access
Journal Browser
Go
American Journal of Pharmacological Sciences. 2015, 3(4), 98-102
DOI: 10.12691/ajps-3-4-3
Open AccessArticle

The Antidepressant-like Action of Human and Caprine Amniotic Fluid in Rats: Effect of Gender

Badreldin H. Ali1, , Abdullah M. Alsaidi1, Saniya El Tayeb2 and Mohamed H. Tageldin3

1Department of Pharmacology and Clinical Pharmacy, College of Medicine and Health Sciences, Sultan Qaboos University, Al-Khod, Muscat, Sultanate of Oman

2Department of Obstetrics and Gynecology, College of Medicine and Health Sciences, Sultan Qaboos University, Al-Khod, Muscat, Sultanate of Oman

3Department of Animal and Veterinary Sciences, College of Agricultural and Marine Sciences, Sultan Qaboos University, Al-Khod, Muscat, Sultanate of Oman

Pub. Date: December 08, 2015

Cite this paper:
Badreldin H. Ali, Abdullah M. Alsaidi, Saniya El Tayeb and Mohamed H. Tageldin. The Antidepressant-like Action of Human and Caprine Amniotic Fluid in Rats: Effect of Gender. American Journal of Pharmacological Sciences. 2015; 3(4):98-102. doi: 10.12691/ajps-3-4-3

Abstract

Depression is a common worldwide burdening mental disease. The amniotic fluid (AF) in both humans and animals has been reported to be associated with reduction of anxiety, pain and with helping the newborns to recognize their mothers. As far as we know, no published work on its possible antidepressant action has been reported before. Therefore, we tested here if AF has an anti-depressant- like activity, and investigated if there is a gender difference in this action. Also, we wanted to find out if this possible action can be modified by a known antidepressant drug. Sixty male and female Wister rats were divided randomly into five groups in each gender, and treated with the following: water (control), human AF, goat AF, venlafaxine and venlafaxine+ human AF. AF and venlafaxine were given orally by gavage at a dose of 0.2ml/ Kgonce a day for five days. Twenty four hours later, locomotor activity test, and the forced swimming test (FST) were measured. Motor activity and immobility time in the FST were both significantly reduced in male and female rats treated with human and caprine AF. Rats treated with human AF showed the least activity. The latter effects were not significantly affected by concomitant treatment with venlafaxine and human AF. The biochemical mechanisms of antidepressant like effect of AF warrant further study.

Keywords:
depression forced swimming test amniotic fluid motor activity rats

Creative CommonsThis work is licensed under a Creative Commons Attribution 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

References:

[1]  ABEL EL: Circannual changes in the duration of the immobility response of rats in the forced swim test. Physiol Behav. 1995; 58:591-593.
 
[2]  ABEL EL. Physical activity does not account for the physiological response to forced swim testing. Physiol Behav. 1994;56:677-681.
 
[3]  AFIFI M: Positive health practices and depressive symptoms among high school adolescents in Oman. Singapore Med J. 2006;47:960-966.
 
[4]  ALI BH, BASHIR AK, TANIRA MO. The effect of Rhazyastricta Decne, atraditional medicinal plant, on the forced swimming test in rats. Pharmacol Biochem Behav. 1998; 59:547-550.
 
[5]  ALI BH, RAMKUMAR A, MADANAGOPAL TT, WALY MI, TAGELDIN M, AL-ABRI S, FAHIM M,YASIN J, NEMMAR A: Motor and behavioral changes in mice with cisplatin-inducedacute renal failure. Physiol Res. 2014; 63:35-45.
 
[6]  ALTEMUS M, SARVAIYA N, NEILL EPPERSON C: Sex differences in anxiety and depression clinical perspectives. Front Neuroendocrinol. 2014;35:320-330.
 
[7]  BOGDANOVA OV, KANEKAR S, D'ANCI KE, RENSHAW PF. Factors influencing behaviorin the forced swim test. PhysiolBehav. 2013;118:227-239.
 
[8]  CONNOR TJ, KELLIHER P, SHEN Y, HARKIN A, KELLY JP, LEONARD BE. Effect ofsubchronic antidepressant treatments on behavioral, neurochemical, and endocrine changes in the forced-swim test. PharmacolBiochemBehav. 2000;65:591-597.
 
[9]  CORONA R, LÉVY F. Chemical olfactory signals and parenthood in mammals. HormBehav. 2014. pii: S0018-506X(14)00134-2.
 
[10]  CRYAN JF, VALENTINO RJ, LUCKI I. Assessing substrates underlying thebehavioral effects of antidepressants using the modified rat forced swimming test. NeurosciBiobehav Rev. 2005;29: 547-569.
 
[11]  LIEBERMAN HR, KELLOGG MD, KRAMER FM, BATHALON GP, LESHER LL. Lipid and otherplasma markers are associated with anxiety, depression, and fatigue. HealthPsychol. 2012;31:210-216.
 
[12]  MCCALL WV, KINTZIGER KW. Late life depression: a global problem with few resources. PsychiatrClin North Am. 2013; 36: 475-481.
 
[13]  O׳LEARY OF, DINAN TG, CRYAN JF. Faster, better, stronger: Towards new antidepressant therapeutic strategies. Eur J Pharmacol. 2014, In press.
 
[14]  PANDEY DK, RAJKUMAR R, MAHESH R, RADHA R. Depressant-like effects ofparthenolide in a rodent behavioural antidepressant test battery. J Pharm Pharmacol. 2008; 60:1643-1650.
 
[15]  OVERSTREET DH. Modeling depression in animal models. Methods Mol Biol.2012; 829: 125-144.
 
[16]  RODRÍGUEZ-LANDA JF, GARCÍA-RÍOS RI, CUETO-ESCOBEDO J, BERNAL-MORALES B, CONTRERAS CM. Participation of GABAA chloride channels in the anxiolytic-like effects of a fatty acid mixture. Biomed Res Int. 2013; 2013: 121794.
 
[17]  SCHAAL B, MARLIER L. Maternal and paternal perception of individual odorsignatures in human amniotic fluid--potential role in early bonding? BiolNeonate. 1998; 74:266-273.
 
[18]  SCAINI G, SANTOS PM, BENEDET J, ROCHI N, GOMES LM, BORGES LS, REZIN GT,PEZENTE DP, QUEVEDO J, STRECK EL. Evaluation of Krebs cycle enzymes in the brain of rats after chronic administration of antidepressants. Brain Res Bull. 2010 31; 82:224-227.
 
[19]  WHITEFORD HA, DEGENHARDT L, REHM J, BAXTER AJ, FERRARI AJ, ERSKINE HE,CHARLSON FJ, NORMAN RE, FLAXMAN AD, JOHNS N, BURSTEIN R, MURRAY CJ, VOS T. Globalburden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010. Lancet. 2013;382(9904):1575-1586.