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Evaluation of Carrot Pomace ( Daucus carota L.) as

Hypocholesterolemic and Hypolipidemic Agent on Albino Rats

Abd El-Moneim M.R. AFIFY

1*

, Ramy R. M. ROMEILAH

1

, Mahmoud M.H. OSFOR

2

, Amir S. M. ELBAHNASAWY

2

1Cairo University, Faculty of Agriculture, Biochemistry Department, P. Box 12613, Gamma Street, Giza, Egypt; [email protected] (*corresponding author)

2National Research Center, Food Science and Nutrition Department, Dokki, Giza, Egypt

Abstract

The current study examined the attenuating influence of dietary carrot pomace powder (CaPP) on hypercholesterolemia and various oxidative stress-associated with biochemical parameters in hypercholesterolemic rats. Thirty two male albino rats weighing 110±10 g were divided into four groups, the first group received the basal diet only and served as (negative control), the second group received the hypercholesterolemic diet and served as positive control, the other groups received hypercholesterolemic diet supplemented with 10%, 20% CaPP for six weeks. The obtained results revealed that groups supplemented with 10% and 20% CaPP significantly decrease total lipid, total cholesterol, triglycerides, low density lipoprotein cholesterol, liver enzymes: alanine aminotransferase, aspartate aminotransferase compared to positive and negative groups. Organs weight, body weight gain significantly decreased compared with positive control. Moreover dietary carrot pomace powder can used to reduce the body weight and reducing hypercholesterolemic complications. In addition, dietary carrot pomace powder serves to improve the blood picture and to reduce the blood glucose level in hypercholesterolemic rats and could use in obese people for body loss. Data of kidney function (Urea) record an increase in CaPP 20%

level (26.9±2.96) but this increase was non significant with the negative control group (26.6±3.1).

Keywords: Daucus carota, hypercholesterolemia, kidney function, obese people

Introduction

Although cholesterol is important and necessary for mammals, but high levels of cholesterol in the blood can damage arteries and are potentially linked to diseases such as those associated with the cardiovascular system and heart disease (Ingelsson et al., 2007).

Fiber is often classified according to its solubility in water into soluble and insoluble dietary fibers (Schnee- man, 2007; Van Way and Ireton-Jones, 2004). Increased dietary fiber intakes are associated with significantly lower prevalence rates of cardiovascular disease (Graham et al., 2007). Soluble fiber, when included within a low saturat- ed fat and cholesterol diet, lowers low-density lipoprotein cholesterol concentration about 5-10% in hypercholester- olaemic and diabetic patients (Anderson et al., 2009). A high intake of fiber, particularly of the soluble type, above the level recommended (25-35 g/day) by the American Dietetic Association (ADA), improves glycemic control, decreases hyperinsulinemia, and lowers plasma lipid con- centrations (Chandalia et al., 2000).

Waste by-products of vegetable food processing rep- resent a major disposal problem in industry (Schieber et al., 2001). Its transformation into value added products,

as fibers may contribute to diminish the problem and to recover valuable biomass and nutrients (Gerschenson et al., 2009).

Carrot (Daucus carota) is an important root vegeta- ble, and usually used for juice production, and there is a steady increase in carrot juice consumption (Schieber et al., 2001). In the juice industry, thousands of tons of car- rot pomace are produced after the juice extraction. Carrot pomace rich in insoluble fiber-rich fraction (56.3 g/100 g of pomace), which was mainly composed of pectic polysac- charides, hemicellulose, and cellulose. This insoluble fiber- rich fraction was found to have desirable physicochemical properties such as high water- and oil-holding capacities, cation-exchange capacity, glucose-adsorbing ability, and amylase inhibition activity (Chau et al., 2004a). Carrot pomace has the highest percentage of soluble fiber when compared with apple, cabbage, strawberry, black currant, and chokeberry pomace (Chantaro et al., 2008; Nawirska and Uklańska, 2008).

Chau et al. (2004b) found that the inclusion of pom- ace fiber in diet effectively decreased the concentrations of serum triacylglycerol, serum total cholesterol, and liver cholesterol, and increased the concentrations of fecal total lipid, fecal cholesterol, and fecal bile acids, and showing Received 28 October 2012; accepted 15 January 2013

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blood hemoglobin, red blood cells (RBCs), white blood cells (WBCs) and hematocrit (HCT), the 2nd heparin- ized tube was centrifuged at 2500 rpm at 37ºC for 15 min to separate the plasma which was kept in the deep freezer for the subsequent investigation. Also, body weight, food consumption were recorded day after day.

Biochemical analysis Lipid profile

Plasma total lipid (TL), triglycerides (TG), total cho- lesterol (TC), low density lipoprotein cholesterol (LDL- C) and high density lipoprotein cholesterol (HDL-C) were determined according to Knight et al. (1972), Fos- sati and Prencipe (1982), Allain et al. (1974), Levy (1981) and Burstein (1970), respectively. Atherogenic Index (AI) was calculated according to Lee and Niemann (1996) us- ing following equation:

Determination of AST, ALT and ALP activities (liver functions)

Aspartate aminotransferase (AST) and alanine ami- notransferase (ALT) activities were measured colori- metrically at 340 nm in plasma according to the method described by Reitman and Frankel (1957). Alkaline phos- phatase (ALP) activity in plasma was determined colori- metrically at 405 nm according to the method of Rec (1972).

Determination of urea and creatinine (kidney functions)

For kidney functions urea in plasma was determined colorimetrically at 578 nm according to the methods de- scribed by Patton and Crouch (1977) and the determina- tion of plasma creatinine content was carried out colori- metrically at 510 nm according to the methods described by Faulkner and King (1976).

Determination of glucose

Plasma glucose level was determined colorimetrically at 510 nm according to Trinder (1969).

Determination of total protein and albumin

Plasma total protein and plasma albumin were de- termined colorimetrically according to the methods de- scribed by Henry (1976) and Doumas and Peters (1997) respectively.

Blood picture Blood hemoglobin

The concentration of blood hemoglobin was deter- mined colorimetrically at 546 nm according to the meth- pronounced hypolipidemic and hypocholesterolemic ef-

fects.

The objectives of this study are to investigate the hypo- cholesterolemic effects of carrot pomace powder in albino rats, furthermore explore the possibility of recycling the waste by-product of food processing to produce a high fi- ber rich product.

Materials and methods Materials

Fresh carrot pomace (Daucus carota) was obtained from local juice extraction shops, and then dried in an air- oven at 45°C for 48 h. The dried pomace was ground in a Multi Mill apparatus and passed through a 0.5-mm mesh sieve to obtain a fine carrot pomace powder.

Chemical composition

The determination of moisture, crude protein, total lipid, ash and crude fibers were done, nitrogen free extract was calculated by difference, deducing the percentage of ash, crude protein, total lipid and crude fibers from 100 according to AOAC (2000).

Biological effects of carrot pomace powder Experimental animals and diets

Thirty two Spraque-Dawley male albino rats weigh- ing 110±10 g were obtained from the laboratory ani- mal house, National Research Center. The animals were housed individually in stainless steel cages in a controlled environment (25±2ºC, 50-60% relative humidity and 12- hour light-dark cycle). The animals were fed ad libitum with a basal diet and water for two weeks, and were then randomly assigned to 4 groups (8 rats each) as follows:

Group 1 (negative control): received basal diet con- sisting of starch 65%, casein 10%, corn oil 10%, salt mix- ture 4%, vitamins mixture 1% and cellulose 10% (AOAC, 2000).

Group 2 (positive control): received hypercholester- olemia-induced diet (high fat diet) which prepared as bas- al diet preparation, except that the 10% corn oil portion was replaced with 10% sheep fat and it was supplemented with 1% cholesterol and 0.25% bile salts (Fukushima et al., 1997).

Group 3: received 80% high fat diet plus 20% carrot pomace powder.

Group 4: received 90% high fat diet plus 10% carrot pomace powder.

Experimental design

During the experimental period (6 weeks), water and diets were available ad libitum. At the end of the experi- ment, all the animals were scarified by cervical decapita- tion. Blood samples were collected in two tubes. The first one (0.5 ml blood) was used for the determination of

C HDL

C HDL l Cholestero Total

(AI) Index c Atherogeni

= −

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od of International Committee for Standardization in Haematology (1967).

Red blood cells (RBCs) and White blood cells (WBCs):

Red blood cells (RBCs) count and White blood cells (WBCs) count were measured according to the method of Natt and Herrick (1952).

Hematocrit (HCT)

Hematocrit (HCT) was determined according to the method of Campbell (1995). Hematocrit is the percent volume of whole blood occupied by red blood cells and is determined by centrifuging blood in special (hematocrit) capillary tubes.

Statistical analysis

Statistical analysis (standard deviation ‘‘SD’’ and standard error ‘‘SE’’) was carried out according to Fisher (1970). LSD (Least significant difference) test was used to compare the significant differences between means of treatment (Waller and Duncan, 1969). The statistical package for social science SPSS (1999) program version was used for all analysis.

Results

Chemical composition

The chemical composition of carrot pomace powder was shown in Tab. 1. The crude fiber content was (11.80%) dry weight basis, the ash content was 6.24%, crude protein 6.86 while total lipid was 1.48% dry weight basis.

Biological effects of carrot pomace powder

Tab. 2 illustrates the body weight gain (BWG), food in- take and feed efficiency ratio (FER) at the end of the study.

The results showed that the addition of CaPP with 10%

level, decreased (BWG) (1.8±0.07), while the addition of CaPP with 20% level was highly significantly decreased (1.0±0.07) than the positive control (2.4±0.06).

It was noticed that, there was no significant changes in food intake among carrot pomace at the level of 20%

(16.8±0.38), 10% (16.7±0.30) and negative control (18.0±0.60), but there was a significant decrease compar- ing with the positive control (20.1±0.33).

Also the feed efficiency ratio (FER) of the 20% CaPP group recorded a significant decrease (0.06±0.00) com- pared with positive control group (0.12±0.00) while

there were no significant changes in 10% CaPP group (0.11±0.00).

On other hand 20% CaPP group showed FER value around the negative control (0.06±0.00 and 0.07±0.00) respectively.

Rats fed on hypercholesterolemia-induced diet devel- oped hypercholesterolemia mark by significant increase in plasma total lipid, triglycerides, total cholesterol, low den- sity lipoprotein cholesterol (LDL-C), and atherogenic In- dex (AI) compared with negative control rats, while high density lipoprotein cholesterol (HDL-C) showed signifi- cant decrease (Tab. 3).

It is obvious that the intake of CaPP with different con- centrations significantly alleviated the total lipid compared with positive control (1252±36.5), but with no significant changes between them (10% and 20%), (609±19.8) and (569±22) respectively.

Total cholesterol recorded high significant decrease in the different concentration of CaPP (10% and 20%) (193±4.15) and (183±4.3) respectively compared with the positive control group (388.9±11.8) while there were non significant changes with the negative control group (199±6.2).

It can be noticed that the intake of CaPP with level 20% recorded some decrease in the total cholesterol than group with 10% and the negative group. In the same table, the triglycerides showed high significant decrease in group 3 (88.9±3.6) and group 4 (109±3.53) compared with the positive control (395±17.2), but the decrease in triglycer- ides of group 3 was non significant as compared with the negative control group (124±7.6).

Data in Tab. 3 demonstrates that the increase in LDL- C was improved by supplementation with CaPP with dif- ferent concentrations to hypercholesterolemic rats. The highest decrease in LDL-C was observed in group fed with 20% CaPP (114±4.05) compared with positive con- trol (324±11.5) and negative control (140±3.4), while the 10% level of CaPP (121±3.92) was non significant com- pared to negative control.

Tab. 1. Chemical composition of carrot pomace as (g/100 g) dry weight basis

Sample Moisture(Air dry) Crude protein Total

lipid Ash Crude

fiber Nitrogen free extract Carrot

pomace 26.5 6.86 1.48 6.24 11.80 73.62

Moisture of fresh carrot pomace was 86.8%

Tab. 2. The mean value of Body Weight Gain, Feed Efficiency Ratio and Food Intake in the experimental rats

Parameters Treatments

Body weight

gaing/d FER Food intake g/d Negative ControlG-1 1.3±0.11 c 0.07±0.00 b 18.0±0.60 b

Positive Control G-2 2.4±0.06 a 0.12±0.00 a 20.1±0.33 a 20% CaPPG-3 1.0±0.07 d 0.06±0.00 b 16.8±0.38 b 10% CaPPG-4 1.8±0.07 b 0.11±0.00 a 16.7±0.30 b All values represented as mean +S.E. Means with different letters are significantly different (p<0.05). * CaPP (carrot pomace powder)

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diet with 20% CaPP (12.8±0.42) compared with negative control (11.2±0.55) and positive control (9.3±0.55) while the tested diet with level 10% CaPP (11.8±0.4) was non significant with negative control. Also the red blood cells (RBCs) recorded no significant changes among the nega- tive control (5.2±0.17) and the group fed with 20% CaPP (5.1±0.15) and 10% CaPP (4.7±0.16), while recorded a significant increase in RBCs compared with the positive control group (3.6±0.18).

Tab. 4 also showed the Hematocrit Value (HCT %).

The CaPP groups with 20% & 10% showed no signifi- cant change compared with negative control (39.4±1.36, 35.5±1.39 and 36.9±2.02) respectively, while they showed a significant increase around the positive control (29.1±1.03).

The white blood cells (WBCs) count represented in the same table. The positive control (3.3±0.24) and the CaPP group with 10% (4.9±0.99) showed significant de- creases compared with negative control (9.6±0.84). On the other hand the value of WBCs count of CaPP group with 20% (7.1±1.42) recorded non significant changes with negative control.

Tab. 5 illustrates the liver functions in the four groups.

The aspartate aminotransferase (AST) showed a high significant decrease in group 3 and 4 (27.8±1.99 and 27.3±1.44) respectively compared with positive control (93.1±6.42), but there were non significant changes with the negative control group (28.4±2.32).

The HDL-C in the pervious table recorded a high sig- nificant increase in group 3 and 4 compared with the posi- tive control (37.8±3.5). It can be noticed that the intake of CaPP with level 20% recorded highly increase in HDL-C (51.5±2.44) but this increase was non significant com- pared with negative control and the 10% CaPP (48.4±3.0 and 47.1±2.36) respectively. Supplementation with 20%

and 10% CaPP showed highly decrease in atherogenic In- dex (AI) which were 2.55 and 3.10 respectively compared with positive control (9.28).

Tab. 4 showed the data of blood picture, it was noticed a significant increase in the hemoglobin among the tested

Tab. 3. Plasma total lipid, total cholesterol, triglycerides, LDL-C, HDL-C (mg/dl) and AI in the experimental rats Parameters

Treatments

Total lipid

(mg/dL) Total cholesterol

(mg/dl) Triglycerides

(mg/dL) LDL-C

(mg/dl) HDL-C

(mg/dl) AI

Negative ControlG-1 631±38.1 b 199±6.2 b 124±7.6 b 140±3.4 b 48.4±3.0 a 3.11

Positive Control G-2 1252±36.5 a 388.9±11.8 a 395±17.2 a 324±11.5 a 37.8±3.5 b 9.28

20% CaPPG-3 569±22 b 183±4.3 b 88.9±3.6 c 114±4.05 c 51.5±2.44 a 2.55

10% CaPPG-4 609±19.8 b 193±4.15 b 109±3.53 bc 121±3.92 bc 47.1±2.36 a 3.10

All values represented as mean +S.E. Means with different letters are significantly different (p<0.05). *CaPP (carrot pomace powder)

Tab. 4. Complete blood picture of the experimental rats Parameters

Treatments

Hemoglobin

(g/dL) RBCs Count

(×million cells /mm³) Hematocrit Value (HCT %)

WBCs Count (×10³ cells /µL)

Negative ControlG-1 11.2±0.55 b 5.2±0.17 a 36.9±2.02 a 9.6±0.84 a

G-2

Positive Control 9.3±0.55 c 3.6±0.18 b 29.1±1.03 b 3.3±0.24 c

20% CaPPG-3 12.8±0.42 a 5.1±0.15 a 39.4±1.36 a 7.1±1.42 ab

10% CaPPG-4 11.8±0.4 ab 4.7±0.16 a 35.5±1.39 a 4.9±0.99 bc

All values represented as mean +S.E. Means with different letters are significantly different (p<0.05). * CaPP (carrot pomace powder)

Tab. 5. Plasma ALT, AST and ALP activities (IU/L) in the experimental rats

Parameters

Treatments AST (IU/L) ALT (IU/L) ALP (IU/L) Negative ControlG-1 28.4±2.32 b 25.6±2.25 b 91±4.81 b

Positive Control G-2 93.1±6.42 a 86±4.04 a 183±4.25 a 20% CaPPG-3 27.8±1.99 b 24±2.23 b 84.5±6.36 b 10% CaPPG-4 27.3±1.44 b 24.8±2.28b 90.4±6.18 b All values represented as mean +S.E. Means with different letters are significantly different (p<0.05).* CaPP (carrot pomace powder)

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(183±4.25) but this value was non significant with nega- tive control (91±4.81).

Data in Tab. 6. represents the results of kidney function tests. Urea records an increase in CaPP with about 20%

level (26.9±2.96) but this increase was non significant with the negative control group (26.6±3.1), on the other side CaPP with 10% level (19.5±2.92) was non significant with the positive control group (12.9±1.73). Also the cre- atinine concentration showed in the same table recorded a significant decrease in 20% CaPP group (0.9±0.06) com- pared with the positive control (1.2±0.07) while the 10%

CaPP group (1.2±0.05) showed non significant changes with the positive control.

The results presented in Tab. 7. indicate the hyperc- holesterolemia effects on blood glucose and plasma total protein and albumin. Total protein recorded a non sig- nificant changes between negative control (7±0.26) and 20% CaPP group (7.5±0.2), while the 10% CaPP showed a significant decrease (6±0.23) which was also significant compared with the positive control (4.2±0.28) which re- corded the lowest value.

Albumin was significantly decreased in 10% CaPP group (3.5±0.18) and positive control (2.5±0.24) com- pared with the 20% CaPP group (4.3±0.17) which was non significant compared with the negative control (4±0.28). In the same table, glucose records an increase in positive control group (105±3.95), this increase in glu- cose level improved by supplementation with 20% CaPP (87.5±3.52) and 10% CaPP (90.5±3.16) this improve reached to the normal level of glucose in negative control group (87±6.67).

Data in Tab. 8. illustrate the organs weight of the ex- perimental rats, supplementations decreased the liver weight in CaPP with 10% (15.0±0.63) and the 20%

level (11.6±0.80) compared with positive control group (20.0±0.85), on the other hand the negative control group recorded the lowest liver weight (9.1±0.27). Kidney has non significant changes in weight between the 10% CaPP group (2.5±0.07) and positive control (2.7±0.06), also the 20% CaPP group (2.3±0.05) showed a value around the negative control (2.2±0.05). Finally, heart and spleen weights showed non significant changes in all groups.

Discussion

Chemical composition of CaPP was shown that Capp is rich in fibers (11.8%) dry weight, results was agree with Bao and Chang (1994) who found that the carrot pomace is rich in fiber more than carrot peels and more that some agriculture by-products such as pear, orange, peach. Also these results are in the same line with Chau et al. (2004a) who found that carrot pomace was rich in dietary fiber and low in protein whereas, the values reported by Holland et al. (1991) for most of these parameters are different i.e.

moisture (88.8%), protein (0.7 %), fat (0.5%), crude fiber (2.4%).

Furthermore, alanine aminotransferase (ALT) was rep- resented in the obvious table. The tested groups recorded non significant changes with the negative control. Nega- tive control was (25.6±2.25), CaPP 20% was (24±2.23) and CaPP 10% (24.8±2.28), on other hand there were a high significant decrease compared with the positive con- trol group (86±4.04). The same results in alkaline phos- phatase (ALP) which showed a very highly significant de- crease in the CaPP groups 10% and 20% (90.4±6.18 and 84.5±6.36) respectively compared with positive control Tab. 6. Plasma urea and creatinine (mg/dL) of the experimental rats

Parameters Treatments

Urea

(mg/dL) Creatinine (mg/dL) Negative ControlG-1 26.6±3.1 a 0.9±0.08 b

G-2

Positive Control 12.9±1.73 b 1.2±0.07 a 20% CaPPG-3 26.9±2.96 a 0.9±0.06 b 10% CaPPG-4 19.5±2.92 ab 1.2±0.05 a All values represented as mean +S.E. Means with different letters are significantly different (p<0.05). * CaPP (carrot pomace powder)

Tab. 7. Plasma protein, albumin (g/dL) and plasma glucose (mg/dL) of the experimental rats

Parameters Treatments

Total protein

(g/dL) Albumin

(g/dL) Glucose (mg/dL) G-1

Negative Control 7±0.26 a 4±0.28 ab 87±6.67 b Positive Control G-2 4.2±0.28 c 2.5±0.24 c 105±3.95 a

G-3

20% CaPP 7.5±0.2 a 4.3±0.17 a 87.5±3.52 b 10% CaPPG-4 6±0.23 b 3.5±0.18 b 90.5±3.16 b All values represented as mean +S.E. Means with different letters are significantly different (p<0.05). * CaPP (carrot pomace powder)

Tab. 8. Relative organs weight (g) of the experimental rats Organs

Treatments Liver Heart Kidney Spleen Negative Control 9.1±0.27 d 1.3±0.06 a 2.2±0.05 b 1.1±0.05 a G-1

Positive Control 20.0±0.85 a 1.4±0.05 a 2.7±0.06 a 1.3±0.06 a G-2 20% CaPPG-3 11.6±0.80 c 1.3±0.07 a 2.3±0.05 b 1.2±0.05 a 10% CaPPG-4 15.0±0.63 b 1.4±0.05 a 2.5±0.07 a 1.2±0.05 a All values represented as mean +S.E.Means with different letters are significantly different (p<0.05). * CaPP (carrot pomace powder)

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The previous results indicated that the rats fed on hy- percholesterolemic diet showed increased liver enzymes (AST, ALT and Alkaline phosphatase). The liver is a cen- tral organ for many physiological and biochemical process necessary for maintenance of life (Souba and Wilmore, 1983). Morphological alterations that occur in the liver affect many metabolic processes in the organism. Peroxide formation induced by hypercholesterolemia (Sudhahar et al., 2007) result in the release of some enzymes by interact- ing with cellular structure and function. Thus, the serum activities of cellular enzymes such as transaminases, alka- line phosphatase, and lactate dehydrogenase do increase.

With the increase in cellular membrane permeability, in- tracellular fluid transfers onto intercellular space, resulting in muscle and liver cell degeneration.

Rats fed on 10 and 20% CaPP supplemented to hy- percholesterolemic diet showed improved liver functions.

AST and ALT levels act as indicators of liver functions, hence, restoration of normal levels of these enzymes indi- cates normal functions of liver. The reduction of AST and ALT close to their normal levels due to consumption of CaPP (Quanhong et al., 2005). The present study also re- vealed that the ALP activity was increased when the liver functions abnormally (Rashad and Moharib, 2008), thus the study of liver ALP was done in the present study to find out the effect of these dietary fiber (CaPP) on liver ALP.

Results showed that CaPP with 10 and 20% had a lowering effect on the activity of ALP in serum of hyperc- holesterolemic rats compared to the positive control, but this decrease was not significant with the negative control group. This effect is mainly related to the presence of natu- ral soluble and insoluble dietary fiber (Rashad and Mo- harib, 2003).

The result of the present study also declared that CaPP especially at 20% level has a significant improvement ef- fect on the kidney functions represented in urea and crea- tinine. This could be explained as consumption of food rich in dietary fibers stimulates the extrarenal route of nitrogen excretion. Younes et al. (1998) found that indi- gestible carbohydrate/dietary fibers increased cecal weight and cecal blood flow, leading to accelerated diffusion of blood urea into the cecal lumen (by threefold), urea lysis to ammonia and protein synthesis by the microflora, and increased fecal excretion of nitrogen. Thus, reduce the role of kidney in the excretion of nitrogen and reduce blood urea concentration.

Total protein and albumin were markedly increased with addition of 10%, 20% CaPP especially with 20%, these results were on a opposite side to Eggum (1992) who reported that dietary fiber had a negative influence on di- gestion and assimilation of proteins. Also results show a markedly decrease of glucose on hypercolesterolemic rats fed on 10 and 20% CaPP. These results were confirmed by Chau et al. (2004a) who found that fiber has functional properties and in vitro hypoglycemic effects. Rodríguez The increase in BWG, FI and FER for positive control

which fed on hypercholesterolemic diet may be due to the presence of animal fat and cholesterol used to increase feeding. Also results revealed that the reduction in BWG of the rats fed on diet containing 20% CaPP indicate mus- cle tissue wasting this decrease may due to high content of fiber, these results were agreed with Parveen et al. (2000) who reported that the fiber content of diet reduce calories and losses weight.

However Chau et al. (2004b) was on an opposite side, they found that consumption of water-insoluble fiber rich fraction didn’t affect the weights of hamsters. Also Nicolle et al. (2003) were on contrary line with our study who found no significant changes on body weight gain and food intake in the groups feed on carrot diet with the con- trol group.

The addition of carrot in the diet with 10, 20% con- centrations lead to decrease in total lipid, total cholesterol, triglycerides and LDL-C but resulting increase of HDL- C. Our data was in the same line with Nicolle et al. (2003) who found carrot consumption exerts a moderate lower- ing cholesterol effect (12% decreases). A significant 11%

reduction of cholesterol has been observed in human sub- jects by Robertson et al. (1979).

Hsu et al. (2006) recorded significant decrease in con- centration of serum triglyceride, serum total cholesterol of hamsters fed on diet containing insoluble fiber-rich frac- tions prepared from carrot pomace. Whereas an absence of effect was reported by Wisker et al. (1994).

The improvement in lipid profile of blood could be re- ferred to a multi factors besides on the role of amino acids of protein, dietary fibers and antioxidants may play a good part in this action. Beneficial treatment of CaPP showed that the dietary fibers are having the potential to lower the levels of total cholesterol and LDL-c in blood. Absorption of bile salts by soluble dietary fiber (SDF) results in chang- es in cholesterol metabolism, loss of cholesterol, unavail- ability of bile salts in the intestine for micelle formation, which inhibits lipid fractions absorption, increased fecal bulk dilutes bile acids in the lower intestinal tract, and short chain fatty acids produced especially the propionate, which has been proposed to inhibit hepatic cholesterol synthesis (Tharanathan and Mahadevamma, 2003).

The improvement in blood picture data was noticed especially in hemoglobin which recorded a significant in- crease in 20% CaPP than control group also hematocrite was in significant increase in 10%, 20% CaPP compared with positive control, this increase in blood picture may due to the high presence of iron. These data were corre- sponding with Sharma et al. (2012) who found that carrot are a good source of minerals like Ca, P, Fe and Mg. Also Gopalan et al. (1991) reported the chemical constituents of carrot as moisture (86%), protein (0.9%), crude fiber (1.2%) and Fe (2.2 mg/100g), Ca (80 mg/100g) and P (53 mg/100g).

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rot insoluble fiber-rich fractions. LWT-Food Sci Technol 37(2):155-160.

Doumas BT, Peters T Jr (1997). Serum and urine albumin: a progress report on their measurement and clinical signifi- cance. Clin Chem Acta 258(1):3-20.

Eggum BO (1992). The influence of dietary fibre on protein digestion and utilisation, 153-165p. In: Schweizer TF, Ed- wards CA (Eds.). Dietary Fibre-A Component of Food. Nu- tritional Function in Health and Disease, Springer-Verlag, London.

Faulkner NR, King JW (1976). Fundamental of clinical chemis- try (2nd ed.) Tietz, Sannders Philadelphia, 994-998 p.

Fisher RA (1970). Statistical method for research workers Edin- burgh ed. 14. Oliver and Boyed, 140 p.

Fossati P, Prencipe L (1982). The determination of triglyceride using enzymatic methods. Clin Chem 28:2077-2080.

Fukushima M, Takayama Y, Habaguchi T, Nakano M (1997).

Comparative hypocholesterolemic effects of capybara (Hy- drochoerus hydrochaeris dabbenei) oil, horse oil and sardine oil in cholesterolfed rats. Lipid 32(4):391-395.

Gerschenson LN, Rojas AML, de Escalada Pla M, Fissore E (2009). Functional properties of dietaryfibre isolated from Cucurbita moschata Duchesne ex Poiret through different extraction procedures, 359-370 p. In: Govil JN, Singh VK (Eds.). Recent Progress in Medicinal Plants. Volume 24 Standardization of herbal/ayurvedic formulations. Texas:

Studium Press LLC.

Gopalan C, Rama Sastri BV, Balasubramanian SC (1991). Nu- tritive value of Indian foods. National institute of Nutrition, ICMR, Hyderabad.

Graham I, Atar D, Borch-Johnsen K (2007). European guide- lines on cardiovascular disease prevention in clinical prac- tice: executive summary. Eur Heart J 28:2375-2414.

Henry RJ (1976). Clinical chemistry, Hoeber, NY, 413 p.

Holland B, Unwin ID, Buss DH (1991). Vegetables, Herbs and Spices. Fifth supplement to McCance and Widdowson’s.

The Composition of Foods, Royal Society of Chemistry, Cambridge, London.

Hsu PK, Chien PJ, Chen CH, Chau CF (2006). Carrot insol- uble fiber-rich fraction lowers lipid and cholesterol absorp- tion in hamsters. LWT-Food Sci Technol 39(4):338-343.

Ingelsson E, Schaefer EJ, Contois JH, McNamara JR, Sullivan L, Keyes MJ, Pencina MJ, Schoonmaker C, Wilson PW, D’Agostino RB, Vasan RS (2007). Clinical utility of differ- ent lipid measures for prediction of coronary heart disease in men and women. JAMA 298(7):776-85.

International Committee for Standardization in Haematology.

(1967). Recommendations for haemoglobinometry in hu- man blood. Brit J Haemat 13(4):71-75.

Knight JA, Anderson SJ, Rawle JM (1972). Chemical bases of the sulfo-phosphovanillin reaction for estimating serum to- tal lipid. Clin Chem 18(3):199-202.

Lee R, Niemann D (1996). Nutritional Assessment 2nd ed Mos- et al. (2006) declared that glucose of diabetic patients de-

creased by having diets rich in fiber. These results given are in a good agreement with Singh et al. (2005) who found that feeding of PoPP at 5% and 10% to diabetic rats signi- cantly decreased their blood glucose level.

It could be noticed from previous results that hyperc- holesterolemia increased organs weight especially liver and kidney compared with negative control, while their spleen and heart had no significant changes in their weight. How- ever, 10% and 20% CaPP supplemented to hypercholes- terolemic treated groups had a significantly decreased in liver and kidney weights.

Conclusions

Finally the present results clearly refer to possibility us- ing carrot pomace powder as hypocholesterolemic agent.

In addition, CaPP also serves to improve the lipid profile (cholesterol, total lipid, triglycerides, LDL-C and HDL- C) and blood picture and to reduce the blood glucose level in hypercholesterolemic rats and could use in obese people for body loss.

References

Allain CC, Poon LS, Chan CS, Richmoud W, Fu PC (1974).

Enzymatic determination of total serum cholesterol. Clin Chem 20(4):470-475.

Anderson JW, Baird P, Davis RH Jr, Ferreri S, Knudtson M, Ko- raym A, Waters V, Williams CL (2009). Health benefits of dietary fiber. Nutr Rev 67(2):188-205.

AOAC (2000). Method of analysis. Association of Official Ag- riculture Chemists. 17th ed, Washington D.C., USA.

Bao B, Chang KC (1994). Carrot pulp chemical composition, colour, and water-holding capacity as affected by blanching.

J Food Sci 59(6):1159-1161.

Burstein M (1970). A fully enzymatic colorimetric determina- tion of HDL cholesterol in the serum. Lipid Res 11:583- 595.

Campbell TW (1995). Avian hematology and cytology, 2nd ed.

Iowa State University Press, Ames, Iowa, 3-19 p.

Chandalia M, Garg A, Lutjohann D, von Bergmann K, Grundy SM, Brinkley LJ (2000). Beneficial effects of high dietary fi- ber intake in patients with type 2 diabetes mellitus. N Engl J Med 342(19):1392-1398.

Chantaro P, Devahastin S, Chiewchan N (2008). Production of antioxidant high dietary fiber powder from carrot peels.

Food Sci Technol 41(10):1987-1994.

Chau CF, Chen CH, Wang YT (2004b). Effects of a novel pom- ace fiber on lipid and cholesterol metabolism in the hamster.

Nutrit Res 24:337-345.

Chau CF, Chen CH, Lee MH, Chau CF, Chen CH, Lee MH (2004a). Comparison of the characteristics, functional properties and in vitro hypoglycemic effects of various car-

(8)

SPSS (1999). Statistical Package for the Social Sciences, version 10, SPSS, Inc., Chicago, Illinois.

Schieber A, Stintzing FC, Carle R (2001). By-products of plant food processing as a source of functional compounds-recent developments. Trends Food Sci Technol 12:401-413.

Schneeman BO (2007). Dietary fiber and gastrointestinal func- tion, 168-176 p. In: Mccleary BV, Prosky L (Eds.). Advanced Dietary Fiber Technology, Black Well Science, Oxford.

Sharma KD, Karki S, Thakur NS, Attri S (2012). Chemical composition, functional properties and processing of carrot- a review. J Food Sci Technol 49(1):22-32.

Singh N, Kamath V, Rajini PS (2005). Protective effect of potato peel powder in ameliorating oxidative stress in streptozoto- cin diabetic rats. Plant Foods Human Nutr 60(2):49-54.

Souba WW, Wilmore DW (1983). Postoperative alteration of arteriovenous exchange of amino acids across the gastroin- testinal tract. Surgery 94(2):342-350.

Sudhahar V, Kumar SA, Sudharsan PT, Varalakshmi P (2007).

Protective effect of lupeol and its ester on cardiac abnormali- ties in experimental hypercholesterolemia. Vascul Pharma- col 46:412-418.

Tharanathan RN, Mahadevamma S (2003). Grain legumes-a boon to human nutrition. Trends Food Sci Technol 14:507- 518.

Trinder P (1969). Determination of blood glucose using an oxi- dation peroxidase system with a non carsinogenic chromo- gene. Ann Clin Biochem 6:24-26.

Van Way CW, Ireton-Jones CS (2004). Nutrition Secrets. 2nd Edition, Hanley and Belfus Inc., Philadelphia. Pennsylvania.

284 p.

Waller RA, Duncan DB (1969). Aboys rule for symmetric mul- tiple comparison problem. An State Assoc J 65:1485-1503.

Wisker E, Schweizer TF, Daniel M, Feldheim W (1994). Fibre- mediated physiological effects of raw and processed carrots in humans. J Nutr 72(4):579-599.

Younes H, Garleb KA, Behr SR, Demigne C, Remesy C (1998).

Dietary fiber stimulates the extrarenal route of nitrogen ex- cretion in partially nephrectomized rats. J Nutr Biochem 9:613-620.

by Missou USA.

Levy AL (1981). A fully enzymatic colourimetric determination of LDL-cholesterol in the serum. Clin Chem 27(5):653- 662.

Natt MP, Herrick CA (1952). A new blood count diluent for counting erythrocytes and leukocytes of the chicken. Poult Sci 31:735-738.

Nawirska A, Uklańska C (2008). Waste products from fruit and vegetable processing as potential sources for food enrich- ment in dietary fibre. Acta Sci Pol Technol Aliment 7(2):35- 42.

Nicolle C, Cardinault N, Aprikian O, Busserolles J, Grolier P, Rock E, Demigné C, Mazur A, Scalbert A, Amouroux P, Rémésy C (2003). Effect of carrot intake on cholesterol metabolism and on antioxidant status in cholesterol-fed rat.

Eur J Nutr 42(5):254-61.

Parveen N, Akhtar MS, Abbas N, Abid AR (2000). Effects of carrot residue fibre on body weight gain and serum lipid fractions. Int J Agri Biol 2:125-128.

Patton CJ, Crouch SR (1977). Spectrophotmetric and kinetics investigations of the Berthelot reaction for the determina- tion of ammonia. Anal Chem 49:464-469.

Quanhong L, Caili F, Yukui R, Guanghui H, Tongyi C (2005).

Effects of protein-bound polysaccharide isolated from pumpkin on insulin in diabetic rats. Plant Foods Hum Nutr 60(1):13-16.

Rashad MM, Moharib SA (2003). Effect of type and level of dietary fiber supplements in rats. Grasas y Aceites 54:277- 284.

Rashad MM, Moharib SA (2008). Studies of the effect of some plant leaf fibers on the key liver enzymes intermediate carbo- hydrate and lipid metabolism in rats. Adv Food Sci 1:1-8.

Rec G (1972). Optimised standard colorimetric methods. J Clin Chem Clin Biochem10:182-185.

Reitman S, Frankel S (1957). A colourimetric method for the determination of serum glutamic oxaloacetic and glutamic pyruvic transaminases. Am J Clin Path 28(56):56-62.

Robertson J, Brydon WG, Tadesse K, Wenham P, Walls A, East- wood MA (1979). The effect of raw carrot on serum lipid and colon function. Am J Clin Nutr 32:1889-1892.

Rodríguez R, Jiménez A, Fernández-Bolaños J, Guillén R, Heredia A (2006). Dietary fibre from vegetable products as source of functional ingredients. Trends Food Sci Technol 17:3-15.

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