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Apple Cider Vinegar Attenuates Lipid Profile in Normal and Diabetic Rats



F. Shishehbor, A. Mansoori, A.R. Sarkaki, M.T. Jalali and S.M. Latifi
 
ABSTRACT

In this study, the effect of apple cider vinegar on Fasting Blood Glucose (FBG), glycated haemoglobin (HbA1c) and lipid profile in normal and diabetic rats was investigated. Diabetes was induced in male Wistar rats (300±30 g) by the intraperitoneal injection of streptozotocin (60 mg kg-1 of body weight). Both normal and diabetic animals were fed with standard animal food containing apple cider vinegar (6% w/w) for 4 weeks. Fasting blood glucose did not change, while HbA1c significantly decreased by apple cider vinegar in diabetic group (p<0.05). In normal rats fed with vinegar, significant reduction of low density lipoprotein-cholesterol (LDL-c) (p<0.005) and significant increase of high density lipoprotein-cholesterol (HDL-c) levels (p<0.005) were observed. Apple cider vinegar also reduced serum triglyceride (TG) levels (p<0.005) and increased HDL-c (p<0.005) in diabetic animals. These results indicate that apple cider vinegar improved the serum lipid profile in normal and diabetic rats by decreasing serum TG, LDL-c and increasing serum HDL-c and may be of great value in managing the diabetic complications.

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F. Shishehbor, A. Mansoori, A.R. Sarkaki, M.T. Jalali and S.M. Latifi, 2008. Apple Cider Vinegar Attenuates Lipid Profile in Normal and Diabetic Rats. Pakistan Journal of Biological Sciences, 11: 2634-2638.

DOI: 10.3923/pjbs.2008.2634.2638

URL: https://scialert.net/abstract/?doi=pjbs.2008.2634.2638

INTRODUCTION

Diabetes mellitus is one of the major chronic disease in all populations (Wild et al., 2004). In addition to hyperglycemia, the most common feature in diabetes is dyslipidemia which is contributed to the development of atherosclerosis (Creager et al., 2003). Therefore, the ideal treatment for diabetes would be an agent that controls the glycemic level and prevents the progression of atherosclerosis. The currently available agents for treatment of diabetes are expensive, not easily accessible and have several side effects (Ramesh and Pugalendi, 2005). Thus, a large number of studies are involved to find natural hypoglycemic and hypolipidemic products as alternatives to the synthetic ones.

Vinegar is produced from fermentable carbohydrate source such as apples, grapes and molasses (Johnston and Gass, 2006). It is commonly used as a food preservative and as a seasoning in different diets (O’Keefe et al., 2008; Hlebowicz et al., 2007). The main component of vinegar is acetic acid, being present at concentrations of 3-5% (Sakakibara et al., 2007). Other constituents of vinegar include some vitamins, mineral salts, amino acids, polyphenolic compounds and organic acids (Johnston and Gass, 2006). Recently, vinegar has been reported to have some beneficial effects on postprandial blood glucose in healthy and diabetic subjects (Johnston et al., 2004; Johnston and Buller, 2005; Ostman et al., 2005; Leeman et al., 2005). Apple cider vinegar which is made by fermentation of apple juice has been used as a folk medicine and its consumption as a home remedy for diabetes is widely advertised in mass media. However, scientific database about its biological effects is scarce. Thus, the present study was conducted to investigate the effect of apple cider vinegar on fasting blood glucose, HbA1-c and lipid profiles in healthy and diabetic rats.

MATERIALS AND METHODS

This study was conducted in July 2005 at Animal Research Center, Ahvaz Jundishapour University of Medical Sciences, Ahvaz, Islamic Republic of Iran.

Animals: Forty male Wistar rats (300±30 g; 4-5 months old) were obtained from the animal research center (Jondyshapour Ahvaz University of Medical Sciences, Ahvaz, Iran). They were housed in the colony in cages (2-3 rats in each cage) under controlled conditions at a room temperature of 22-24°C, 55-60% humidity and a 12 h light/dark cycle. Standard animal pellets (Chavdane, Shahreza, Iran) and tap water were provided ad libitum. Nine rats died accidentally because of diabetes, so the provided results were from 31 rats.

Induction of diabetes: Streptozotocin (STZ) was purchased from Sigma-Aldrich (St. Louis, United State). Diabetes was induced by intraperitoneal injection of a single dose of streptozotocin (60 mg kg-1 b.wt.) dissolved in normal saline (Yamamoto et al., 2000). The control rats received only the same volume of saline. STZ-injected animals were allowed to drink 4.5 g L-1 sodium chloride solution instead of water for the whole period of treatment to prevent diuresis and were given 5% glucose solution in the 3rd day after STZ ingestion to prevent hypoglycemic mortality (Khaksari et al., 2004). Diabetes was confirmed by measuring fasting blood glucose, 6 days after STZ injection. The animals with blood glucose ≥150 mg dL-1 were considered to be diabetic (Trivedi et al., 2004).

Treatment diet: Apple cider vinegar (Yeko-Yek, Iran) was purchased from local shop containing 4.4 g dL-1 acetic acid. The animal pellets were powdered by a kitchen blender and mixed with apple cider vinegar (6 g vinegar/100 g animal food) (Kondo et al., 2001). This mixture was then transformed into a pellet form using an industrial meat mincer. The pellets were then dried at room temperature and used for the experiment. The treatment was started on the day 8th after STZ-injection and continued for 4 weeks.

Experimental design: The animals were randomly divided into four groups of ten, classified as: normal: normal rats treated with apple cider vinegar, diabetic control: diabetic rats treated with apple cider vinegar. Blood samples (2-3 mL) were collected after 12 h fasting from the tail vein under ketamine anesthesia (90 mg kg-1, i.p.), before and after the treatment period (end of the 4th week).

Serum was separated by centrifugation at 3000 x g at 4°C for 15 min and stored at -20°C for biochemical analysis. Fasting blood glucose, Total Cholesterol (TC), triglyceride and high density lipoprotein cholesterol concentrations were determined by enzymatic colorimetric assays using commercially available kits (Pars Diagnostics, Iran). Low density lipoprotein cholesterol was estimated using Freidewald formula (Friedewald et al., 1972). The concentration of HbA1-c in whole blood was measured by ion-exchange column chromatography (Hb-Gold system, Italy).

Statistical analysis: All results are presented as the Mean±SD. Statistical analysis were performed with the SPSS software (version 15 SPSS Inc, Chicago, IL). The comparisons of mean values within a group were performed using paired t-test, whereas those between the groups were assessed using independent sample t-test. The p-values of <0.05 were considered significant.

RESULTS

FBG and HbA1-c: As shown in Table 1, initial values for FBG were similar in normal rats and remained unchanged after intervention with apple cider vinegar. Diabetic rats exhibited elevated level of blood glucose as compared with normal rats (p<0.05). Although, diet containing apple cider vinegar had no significant effect on FBG, it resulted in a significant decrease in HbA1-c by 18.8% in diabetic rats (p<0.05).

Lipid profiles: The total serum cholesterol did not change in any group (Table 2, 3). In normal rats treated with apple cider vinegar, 47% reduction in LDL-c levels (p<0.005) and 34% increase in HDL-c levels (p<0.005) were observed. Significant differences in these parameters were also observed in respect to normal rats (p<0.005) (Table 2).

There was a marked elevation in serum TG concentration (1.8 fold) after STZ injection in diabetic control group (p<0.005). However, supplementation with apple cider vinegar significantly reduced the serum TG compared with control group (Table 3). Serum HDL-c was significantly reduced in diabetic control rats (compared with initial values), however treatment with vinegar resulted in a marked elevation (18%) in HDL-c in diabetic animals (p<0.05).

Table 1: Concentrations of Fasting Blood Glucose (FBG) and HbA1-c before and after 4 weeks treatment with apple cider vinegar in normal and diabetic rats
Data are expressed as Mean±SD. ap<0.05 as compared to initial values (before). bp<0.05 as compared to control group. Normal+vinegar: Normal rats treated with apple cider vinegar; Diabetic+vinegar: Diabetic rats treated with apple cider vinegar

Table 2: Concentrations of serum triglyceride (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDL-c) and low density lipoprotein cholesterol (LDL-c) before and after 4 weeks treatment with apple cider vinegar in normal rats
Data are expressed as Mean±SD. ap<0.005 as compared to initial values (before). bp<0.005 as compared to normal rats treated with apple cider vinegar (Normal+vinegar)

Table 3: Concentrations of serum triglyceride (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDL-c) and low density lipoprotein cholesterol (LDL-c) before and after 4 weeks treatment with apple cider vinegar in diabetic rats
Data are expressed as Mean±SD. ap<0.005 as compared to initial values (before). b p<0.005 as compared to control group. cp<0.05 as compared to initial values (before). Diabetic+vinegar: Diabetic rats treated with apple cider vinegar

DISCUSSION

Results from the present study indicated that feeding a diet containing apple cider vinegar has a beneficial effect on serum lipid profiles of normal and diabetic rats. HbA1-c levels were also reduced in diabetic rats. However, the fasting blood glucose concentration was not altered by apple cider vinegar. Present results regarding HbA1c is consistent with the findings by Sakakibara et al. (2007), who reported a significant reduction of HbA1-c by acetic acid-mixed diet in diabetic KK-A(y) mice. Johnston et al. (2009) was also found that daily consumption of vinegar at meal time reduced the HbA1-c values in diabetic patients. The improved HbA1-c levels by vinegar could be explained by the effect of acetic acid (its main component) in lowering the glycemic index of diet (Ostman et al., 2005; Sugiyama et al., 2003). It has been demonstrated that the consumption of diets with low glycemic index improve HbA1-c in subjects with type 2 diabetes (Wolever et al., 1992; Brand-Miller et al., 2003). These results suggest that vinegar may improve glycemic control. However, this is contrary to the result of the earlier study that showed no changes in HbA1-c after administration of white vinegar (Shishehbor et al., 2007). Further studies will be required to confirm the beneficial effects of vinegar on FBG and HbA1-c.

Diabetes mellitus is associated with profound alterations in plasma lipid and lipoprotein profile which are considered as risk factors for coronary heart disease (Betteridge, 1997; Creager et al., 2003). Increased plasma TG and reduced HDL-c levels are the key characteristics of dyslipidemia in type 2 diabetes (Lehto et al., 1997). The current study showed that the administration of apple cider vinegar decreased the elevated plasma TG levels in diabetic rats. This is consistent with the finding by Bender et al. (2002), who reported that oral administration of apple cider vinegar to normal mice induced a significant reduction in plasma TG levels. Similar results were also observed in the earlier study in diabetic rats treated with white vinegar (Shishehbor et al., 2007). Furthermore, Fushismi et al. (2006) have reported that acetic acid lowered serum TG in rats which were fed a cholesterol-rich diet. Although higher plasma TG concentrations in diabetic mice treated with acetic acid were observed by Sakakibara et al. (2007), while TG levels in the liver was significantly decreased. Taken together, these results indicate that ingestion of vinegar may affect plasma TG concentrations. The hypotriglyceridemic effect of apple cider vinegar might be due to the reduction of hepatic TG storage (Bender et al., 2002). This could be further supported by the findings of Fushismi et al. (2006), who reported that dietary acetic acid reduces serum TG concentrations in rats through inhibition of lipogenesis in the liver, together with a concomitant enhancement of fatty acid β-oxidation.

The observed reduction in plasma triglyceride seen in diabetic rats was paralleled by increased plasma HDL-c concentration. Furthermore, apple cider vinegar lowered serum LDL-c and increased serum HDL-c in normal rats. These remarkable effects were also induced by white vinegar in normal rats in the earlier experiment (Shishehbor et al., 2007). The possible mechanism attributed to these findings could be related to the lowering effect of vinegar/or acetic acid on the glycemic index (Ostman et al., 2005; Sugiyama et al., 2003). It has been found that the lower glycemic index diets are able to increase HDL-c and reduce LDL-c levels (Leeds, 2002; Slyper et al., 2004). Furthermore, the low glycemic diet has been shown to decrease serum LDL-c concentrations in diabetic patients (Jarvi et al., 1999). Ford and Liu (2001) also reported an inverse relation between dietary glycemic index and plasma HDL-c concentrations in adults. The results of the present study might also be due to the effect of polyphenols in apple cider vinegar (Kahle et al., 2006). Apple polyphenols have been shown to decrease the serum LDL-c levels in healthy human (Nagasako-Akazome et al., 2007) and increase the serum HDL-c in rats (Osada et al., 2006) and in hamsters (Lam et al., 2008). These changes in HDL-c and LDL-c concentrations could be possibly contributed to the suppression of intestinal lipoprotein secretion by apple polyphenols (Vidal et al., 2005). These results suggest that apple cider vinegar may improve lipoprotein pattern not only by lowering the glycemic index but also by its polyphenolic compounds.

Findings of the present study show a favorable effect of apple cider vinegar on plasma lipoprotein modification managing the diabetic complications.

ACKNOWLEDGMENTS

This study is a part of the M.Sc Project of Anahita Mansoori. The study was supported by grant No. 84U38 of the Ahvaz Joundishapour University of Medical Sciences, Ahvaz, Islamic Republic of Iran. We thank Azar Mostofi and Ahmad Zand-Moghadam for technical assistance.

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