Journal of Clinical and Diagnostic Research, ISSN - 0973 - 709X

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Original article / research
Year : 2018 | Month : June | Volume : 12 | Issue : 6 | Page : FC06 - FC10

Correlation of Gender and Leptin with Analgesic Effect of Tramadol in High Fat Diet Induced Obese Rats

Shakta Mani Satyam, Laxminarayana Kurady Bairy, Vasudha Devi

1. Lecturer, Department of Pharmacology, Melaka Manipal Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India. 2. Associate Dean (Basic Sciences), Professor and Chairperson, Department of Pharmacology, RAK College of Medical Science, Ras al-Khaimah, United Arab Emirates. 3. Professor and Head, Department of Pharmacology, Melaka Manipal Medical College, Manipal Academy of Higher Education, Manipal, Karnataka, India.

Correspondence Address :
Dr. Shakta Mani Satyam,
Lecturer, Department of Pharmacology, Melaka Manipal Medical College, Manipal Academy of Higher Education,
Manipal-576104, Karnataka, India.
E-mail: smsatyam21@gmail.com

Abstract

Introduction: Gender and obesity related influences on the experience of pain have received considerable empirical attention in recent years. Differences in pain sensitivity among individuals may have implications for pain management which might account in part for the variability in analgesic requirements between individuals.

Aim: To investigate the correlation of gender and serum leptin level with analgesic modulation of tramadol in high fat diet induced obese Wistar rats.

Materials and Methods: A total of 48 Wistar rats (24 each male and female; body weight 100-150 gm) were housed as two rats/ cage. In addition to the normal pellet diet, these animals were orally fed with a mixture of Vanaspati daalda+Coconut oil (3:1)- 10 mL/kg/day for 90 days. After 90 days, these rats attained body weight approximately =300 gm (obese). Thereafter, each 24 male and 24 female obese rats were randomly divided into two groups (n=6/group) (Group I- Control: 0.9% NaCl; 1 mL/kg/ day i.p. and Group II- Test: Tramadol 10 mg/kg/day i.p.) for each nociception model-plantar test (12 male rats and 12 female rats) and acetic acid induced writhing test (12 male rats and 12 female rats). The treatment duration was of five days.

Results: Paw Withdrawal Latency (PWL) was significantly decreased (p<0.001) and both number of writhing movements and serum leptin concentrations were significantly increased (p<0.001) in obese female control group compared to obese male control group. Tramadol treated both obese male and female rats had significantly increased PWL (p<0.001) and decreased both number of writhing movements and serum leptin concentration (p<0.001) in comparison with both obese male and female control groups respectively. In tramadol treated obese female rats, PWL was significantly decreased (p=0.048) and both number of writhing movements and serum leptin concentration were significantly increased (p<0.001) in comparison with the tramadol treated obese male rats. PWL was negatively correlated with serum leptin concentration (Pearson correlation coefficient= -0.754, 2-tailed significance; p<0.001), and number of writhing movements were positively correlated with serum leptin concentration (Pearson correlation coefficient=0.507, 2-tailed significance; p=0.011).

Conclusion: The present study revealed that obese female rats have more serum leptin concentration than obese male rats which could be one of the possible reasons for having more pain sensation to noxious stimuli in obese female rats compared to obese male rats. Tramadol treatment at the dose of 10 mg/ kg for five days has decreased serum leptin level in rats which might be one of the additional analgesic mechanisms of action of tramadol.

Keywords

Acetic acid, Obesity, Opioids, Pain threshold, Plantar, Sex hormone, Writhing test

How to cite this article :

Shakta Mani Satyam, Laxminarayana Kurady Bairy, Vasudha Devi. CORRELATION OF GENDER AND LEPTIN WITH ANALGESIC EFFECT OF TRAMADOL IN HIGH FAT DIET INDUCED OBESE RATS. Journal of Clinical and Diagnostic Research [serial online] 2018 June [cited: 2018 Jun 23 ]; 12:FC06-FC10. Available from
http://www.jcdr.net/back_issues.asp?issn=0973-709x&year=2018&month=June&volume=12&issue=6&page=FC06-FC10&id=11668

DOI and Others

DOI: 10.7860/JCDR/2018/36789.11668

Date of Submission: Apr 14, 2018
Date of Peer Review: May 07, 2018
Date of Acceptance: May 26, 2018
Date of Publishing: Jun 01, 2018

FINANCIAL OR OTHER COMPETING INTERESTS: None.

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