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Trends in Medical Research

Year: 2016 | Volume: 11 | Issue: 2 | Page No.: 82-87
DOI: 10.17311/tmr.2016.82.87
Curcumin Intake Could Lower Serum Macrophage Migration Inhibitory Factor and Monocyte Chemoattractant Protein-1 Levels in Obese Subjects
Nagwa Abdallah Ismail , Soha M. Abd El Dayem, Mona Hamed, Dina F. Ayoub, Eman Mahmoud Hassan and Heba Assal

Abstract: Controlling of inflammatory process associated with obesity is a big challenge. Both Monocyte Chemoattractant Protein-1 (MCP-1) and macrophage Migration Inhibitory Factor (MIF) may play a role in this process. Aim to evaluate serum MPC-1 and MIF levels in obese subjects and detect the effect of oral curcumin intake. The study included 60 obese subjects (30 children and 30 adults). The trial subjects received a 500 mg curcumin capsule with the main meal for 4 weeks. Controls received a placebo capsule for 4 weeks. A total of 60 normal weights enrolled as controls. The MIF and MCP-1 levels were measured on days 1 and 29 using commercially available ELISA kits. The mean serum level of MPC-1 and MIF were significantly higher in obese group than in controls. Curcumin intake resulted in statistically significant decrease in serum MPC-1 and serum MIF in children and adults. Our results showed that curcumin could help in lowering MIF and MPC-1 associated with obesity. It could help in prevention of obesity complications.

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How to cite this article
Nagwa Abdallah Ismail, Soha M. Abd El Dayem, Mona Hamed, Dina F. Ayoub, Eman Mahmoud Hassan and Heba Assal, 2016. Curcumin Intake Could Lower Serum Macrophage Migration Inhibitory Factor and Monocyte Chemoattractant Protein-1 Levels in Obese Subjects. Trends in Medical Research, 11: 82-87.

Keywords: MIF, MPC-1, curcumin and Obesity

INTRODUCTION

The prevalence of obesity is increasing rapidly in most countries and is an urgent public health problem (Black et al., 2013; Ng et al., 2014). Complications of obesity are a big problem nowadays. Obesity is associated with many health complications and an increased risk of premature onset of illnesses, including diabetes and heart disease (Ezzat et al., 2012; Lobstein and Jackson-Leach, 2006; Azza et al., 2011). Avoiding childhood obesity is the main target to prevent non-communicable diseases and its psychological effects in children and adults and the trans-generational risk of developing obesity.

Macrophage Migration Inhibitory Factor (MIF) is an innate cytokine involved in many inflammatory and autoimmune disorders. It has been implicated as a causal mechanism in a number of disease conditions including cardiovascular and kidney disease (Zernecke et al., 2008; Lan, 2008). The MIF is widely expressed in numerous types of tissue and it regulates acute inflammatory as well as adaptive immune reactions (Flaster et al., 2007; Cheng et al., 2007). Increasing evidence suggests that MIF could control metabolic and inflammatory processes.

Monocyte Chemoattractant Protein-1 (MCP-1) is secreted by macrophages and endothelial cells and is a potent chemotactic factor for monocytes (Yoshimura et al., 1989; Deshmane et al., 2010). Sartipy and Loskutoff (2003) reported that there was abundance of MCP-1 in both adipose tissue and plasma in obese mice, suggesting that MCP-1 might play an important role in obesity.

Curcumin has a wide range of functions mainly antioxidant; antitumor, anti-inflammatory properties (Anto et al., 2002; Lan, 2008; Sandur et al., 2007). It could modify various targets involved in obesity and associated metabolic diseases (Ismail et al., 2014).

Aim to evaluate to evaluate both serum MPC-1 and MIF in obese subjects and detect the effect of oral curcumin intake.

MATERIAL AND METHODS

The study protocol was approved by the Human Ethics Committee of National Research Centre (NRC), Egypt. Written informed consent was obtained from parent of each child and adult subjects before enrolment. Thirty obese children, defined by BMI >95th percentile for age and sex (Ghalli et al., 2008) were enrolment. Also 30 obese adults with BMI >30 were included. They met the following eligibility criteria: age 10-18 years for children and age 20-40 years for adults. Exclusion criteria were acute infection, hypothyroidism and obesity associated with syndromes. Obese subjects suffering from other autoimmune diseases, malignancy or receiving immunosuppressive drugs were also excluded. We divided obese subjects randomly into a trial group and a control group.

The trial subjects received a 500 mg curcumin capsule with the main meal for 4 weeks (Ismail et al., 2014). Controls received a placebo capsule for 4 weeks.

Another group of 30 children and 30 adults with normal weight serving as controls for laboratory results. They must be healthy and free from acute infections.

All subjects included in this study were subjected to full history taking, thorough clinical examination, with emphasis on blood pressure measured according to American Heart Association guidelines, anthropometric indices: Body weight measured to the nearest 0.1 kg with a balance scale and height measured to the nearest 0.1 cm. Body Mass Index (BMI) was calculated as weight divided by height squared (kg m‾2). Waist Circumference (WC) and hip circumference (HIP C) were measured.

Child body fat (%) = (1.51×BMI)-(0.70×age)-(3.6×gender)+1.4

Adult body fat (%) = (1.20×BMI)+(0.23×age)-(10.8×gender)-5.4

where, female = 0 and male = 1 (Deurenberg et al., 1991).

Laboratory measurements: Each subject gave fasting blood samples on days 1 and 29. Blood samples were centrifuged and serum was stored at -80°C.

Routine investigation including CBC, thyroid profile, liver and kidney functions were done.

Evaluation of serum MIF and MCP-1 levels were done by commercially available ELISA kits (MIF: Hangzhou East biopharma Co. Ltd., China, MCP-1: Sun red Biological Technology, China) according to the manufacturer’s instructions.

Statistical analysis: Conducted using Statistical Package for Social Science (SPSS) program version 15.0 (Chicago, IL, USA). All numeric variables were expressed as Mean±Standard Deviation (SD). Comparison of different variables in various groups was done using Student t test for normal variable. Pearson's and Spearman's correlation tests (r = correlation coefficient) were used for correlating normal and non-parametric variables, respectively. To assess the effect of oral curcumin vs. placebo, the paired sample t test was used to compare means for normally distributed data. The p-values <0.05 were considered as statistically significant.

RESULTS

The study included 60 obese subjects (30 children and 30 adults). Obese children mean age was 14.71±4.52 years, male/female 9/21. Obese adults mean age was 37.55±9.93 years, male/female11/19. A total of 60 normal wt. enrolled as controls. Thirty children their mean age was12.241±3.11 years, male/female 11/19. Thirty adults their mean age was 34.35±10.75 years, male/female 10/20. Table 1 shows a comparison between obese subjects and controls as regard to anthropometric measurements. We found a significant difference (p = 0.000) between both groups. The mean level of MIF was higher in obese subjects than in controls 7.90±3.88, in children 4.46±1.98 ng mL–1 and in adults 7.08±2.45, 5.04±1.93 ng mL–1, p = 0.000. As regard, the mean serum level of MPC-1 it was significantly higher in obese group than in controls. In children the mean value was 21.57±11.10 vs 7.38±4.09 pg mL–1, respectively, p = 0.002. In adults the mean value was 38.20±54.04 vs 9.25±3.53 pg mL–1, respectively, p = 0.018.

The MCP-1 was correlated significantly with BMI, WHTR, percentage body fat and MIF in adults (r = 0.418, 0.292, 0.393, 0.425, respectively and p = (0.001, 0.026, 0.002 and 0.001, respectively). Obese children showed similar correlation (Table 2).

Table 3 shows the results of comparison between curcumin intake group versus placebo group in children and adults. No significant variation was detected between groups.

Trial results are shown in Table 4 and Fig. 1a-b and 2a-b. Curcumin intakes resulted in statistically significant decrease in serum MPC-1 and serum MIF in children and adults. As regard, the placebo group no significant change was observed (Table 5).

Table 1: Comparison between obese children and adults and normal weight controls
Sig: Significant, SD: Standard deviation, BMI: Body mass index, MPC-1: Monocyte chemoattractant protein-1 and MIF-1: Migration inhibitory factor-1

Table 2: Correlation between MPC-1 and MIF with indices of obesity in children and adults
Sig: Significant, BMI: Body mass index, WHTR: Waist to height ratio, PBF: Percent body fat, MPC-1: Monocyte chemoattractant protein-1 and MIF-1: Migration inhibitory factor-1

Table 3: Comparison between curcumin intake group versus placebo group in children and adults
BMI: Body mass index, SD: Standard deviation, Sig: Significant, MPC-1: Monocyte chemoattractant protein-1 and MIF-1: Migration inhibitory factor-1

Table 4: Effect of curcumin intake in children and adults
SD: Standard deviation, Sig: Significance, MPC-1: Monocyte chemoattractant protein-1, MIF-1: Migration inhibitory factor-1 and MIF-2: Migration inhibitory factor-2

Table 5: Effect of placebo intake in children and adults
SD: Standard deviation, Sig: Significance, MPC-2: Monocyte chemoattractant protein-2, MPC-1: Monocyte chemoattractant protein-1, MIF-1: Migration inhibitory factor-1 and MIF-2: Migration inhibitory factor-2

DISCUSSION

Recently, it had been reported that MIF and MPC-1could have a role in the inflammatory process in obesity (Lue et al., 2002; Deshmane et al., 2010). The work was aiming to evaluate both serum MPC-1 and MIF in obese subjects and detect the effect of oral curcumin intake.

The study showed that both circulating MPC-1 and MIF levels were statistically significantly higher in obese children and adults. Same results reported by other authors (Bruun et al., 2005).

Fig. 1(a-b): Effect of curcumin in adults

Fig. 2(a-b): Effect of curcumin in children

Serum MPC-1 was correlated with indices of obesity as BMI and percentage body fat in all obese subjects. Bruun et al. (2005) supported our result and explained it by the fact that MCP-1 is partially produced from the adipocyte fraction which is more in obese subject. Also, Weight loss in obese subjects could to lower serum MIF concentrations.

After curcumin intake obese subjects had significant improvements in serum MIF and MPC-1 levels. Pan et al. (2004) reported that increased serum MIF concentrations appear to be associated with β-cell dysfunction. Several vitro studies proved that MIF had a role in glucose metabolism. Benigni et al. (2000) found that serum MIF increased catabolism in skeletal muscles. Improvements in MIF may be a sign of improving β-cell function.

The MCP-1 secreted by fat cells especially visceral fat was highly regulated and increased by proinflammatory cytokines and chemokines (Murao et al., 1999). Sandur et al. (2007) and Ismail et al. (2014) supported our result as they found that curcumin has an anti-inflammatory function.

The study has some limitations such as small number of cases and short duration of curcumin intake. Also the study did not evaluate how long this effect persists. Promising result is encouraging to perform a big study for a longer duration.

CONCLUSIONS

Circulating MIF and MPC-1 concentrations were significantly elevated in obese children and adults. Oral intake of curcumin could lower the circulating MIF and MPC-1 levels so it could decrease obesity associated complications.

ACKNOWLEDGMENT

The study was a part of a project supported financially by National Research Centre Fund (NRC) Egypt, grant no. 9090102.

REFERENCES

  • Anto, R.J., A. Mukhopadhyay, K. Denning and B.B. Aggarwal, 2002. Curcumin (diferuloylmethane) induces apoptosis through activation of caspase-8, BID cleavage and cytochrome c release: Its suppression by ectopic expression of Bcl-2 and Bcl-xl. Carcinogenesis, 23: 143-150.
    CrossRef    PubMed    Direct Link    


  • Azza, M.A., S.H. Ragab, N.A. Ismail, M.A.M. Awad and M.E. Kandil, 2011. Echocardiographic assessment of epicardial adipose tissue in obese children and its relation to clinical parameters of the metabolic syndrome. J. Clin. Basic Cardiol., 14: 7-11.
    Direct Link    


  • Benigni, F., T. Atsumi, T. Calandra, C. Metz, B. Echtenacher, T. Peng and R. Bucala, 2000. The proinflammatory mediator macrophage migration inhibitory factor induces glucose catabolism in muscle. J. Clin. Invest., 106: 1291-1300.
    PubMed    Direct Link    


  • Black, R.E., C.G. Victora, S.P. Walker, Z.A. Bhutta and P. Christian et al., 2013. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet, 382: 427-451.
    CrossRef    Direct Link    


  • Bruun, J.M., A.S. Lihn, S.B. Pedersen and B. Richelsen, 2005. Monocyte chemoattractant protein-1 release is higher in visceral than subcutaneous human Adipose Tissue (AT): Implication of macrophages resident in the AT. J. Clin. Endocrinol. Metab., 90: 2282-2289.
    PubMed    Direct Link    


  • Cheng, Y., A. Kozubek, L. Ohlsson, B. Sternby and R.D. Duan, 2007. Curcumin decreases acid sphingomyelinase activity in colon cancer Caco-2 cells. Planta Medica, 73: 725-730.
    CrossRef    PubMed    Direct Link    


  • Deurenberg, P., J.A. Weststrate and J.C. Seidell, 1991. Body mass index as a measure of body fatness: Age- and sex-specific prediction formulas. Br. J. Nutr., 65: 105-114.
    CrossRef    PubMed    Direct Link    


  • Ezzat, W.M., S. Ragab, N.A. Ismail, Y.A. Elhosary, A.M.N.E. Abd ElBaky, H. Farouk and I.A. Rasheed, 2012. Frequency of non-alcoholic fatty liver disease in overweight/obese children and adults: Clinical, sonographic picture and biochemical assessment. J. Genet. Eng. Biotechnol., 10: 221-227.
    CrossRef    Direct Link    


  • Flaster, H., J. Bernhagen, T. Calandra and R. Bucala, 2007. The macrophage migration inhibitory factor-glucocorticoid dyad: Regulation of inflammation and immunity. Mol. Endocrinol., 21: 1267-1280.
    CrossRef    Direct Link    


  • Ismail, N.A., S. Ragab, A.N.E. Abd El Baky, M. Hamed and A.S.A. Ibrahim, 2014. Effect of oral curcumin administration on insulin resistance, serum resistin and fetuin-A in obese children: Randomized placebo-controlled study. Res. J. Pharmaceut. Biol. Chem. Sci., 5: 887-896.
    Direct Link    


  • Lan, H.Y., 2008. Role of macrophage migration inhibition factor in kidney disease. Nephron Exp. Nephrol., 109: e79-e83.
    CrossRef    PubMed    Direct Link    


  • Lobstein, T. and R. Jackson-Leach, 2006. Estimated burden of paediatric obesity and co-morbidities in Europe. Part 2. Numbers of children with indicators of obesity-related disease. Int. J. Pediatr. Obesity, 1: 33-41.
    CrossRef    Direct Link    


  • Lue, H., R. Kleemann, T. Calandra, T. Roger and J. Bernhagen, 2002. Macrophage migration inhibitory factor (MIF): Mechanisms of action and role in disease. Microbes Infect., 4: 449-460.
    CrossRef    Direct Link    


  • Murao, K., H. Imachi, A. Momoi, Y. Sayo and H. Hosokawa et al., 1999. Thiazolidinedione inhibits the production of monocyte chemoattractant protein-1 in cytokine-treated human vascular endothelial cells. FEBS Lett., 454: 27-30.
    CrossRef    Direct Link    


  • Ng, M., T. Fleming, M. Robinson, B. Thomson and N. Graetz et al., 2014. Global, regional and national prevalence of overweight and obesity in children and adults during 1980-2013: A systematic analysis for the Global burden of disease study 2013. Lancet, 384: 766-781.
    CrossRef    Direct Link    


  • Pan, J.H., G.K. Sukhova, J.T. Yang, B. Wang and T. Xie et al., 2004. Macrophage migration inhibitory factor deficiency impairs atherosclerosis in low-density lipoprotein receptor-deficient mice. Circulation, 109: 3149-3153.
    CrossRef    Direct Link    


  • Sartipy, P. and D.J. Loskutoff, 2003. Monocyte chemoattractant protein 1 in obesity and insulin resistance. Proc. Natl. Acad. Sci. USA., 100: 7265-7270.
    CrossRef    PubMed    Direct Link    


  • Sandur, S.K., H. Ichikawa, M.K. Pandey, A.B. Kunnumakkara, B. Sung, G. Sethi and B.B. Aggarwal, 2007. Role of pro-oxidants and antioxidants in the anti-inflammatory and apoptotic effects of curcumin (diferuloylmethane). Free Radic. Biol. Med., 43: 568-580.
    CrossRef    Direct Link    


  • Deshmane, S.L., S. Kremlev, S. Amini and B.E. Sawaya, 2010. Monocyte Chemoattractant Protein-1 (MCP-1): An overview. J. Interferon Cytokine Res., 29: 313-326.
    CrossRef    Direct Link    


  • Yoshimura, T., E.A. Robinson, S. Tanaka, E. Appella, J. Kuratsu and E.J. Leonard, 1989. Purification and amino acid analysis of two human glioma-derived monocyte chemoattractants. J. Exp. Med., 169: 1449-1459.
    CrossRef    Direct Link    


  • Zernecke, A., J. Bernhagen and C. Weber, 2008. Macrophage migration inhibitory factor in cardiovascular disease. Circulation, 117: 1594-1602.
    CrossRef    Direct Link    


  • Ghalli, I., N. Salah, F. Hussien, M. Erfan and M. El-Ruby et al., 2008. Egyptian Growth Curves 2002 for Infants, Children and Adolescents. In: Crescere Nel Mondo, Sartorio, A., J.M.H. Buckler and N. Marazzi (Eds.)., Ferring Publisher, Italy

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