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Research Article
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Proximate and Fatty Acid Composition of the Liver of Cultured Asian Redtail Catfish (Hemibagrus nemurus) and African Catfish (Clarias gariepinus) |
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H. Abdi,
A. Christianus,
E. Ramezani- Fard,
C.R. Saad
and
S.A. Hosseini
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ABSTRACT
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Catfish species are popular fish group consumed in Malaysia. African catfish, Clarias gariepinus and Asian redtail catfish, Hemibagrus nemurus are two of these catfish species. Unfortunately, some parts of these fish are removed during processing. This includes the liver which contained considerable amount of extractable lipid with both monounsaturated and polyunsaturated fatty acids. The fish samples were purchased and transported in ice box to the laboratory. Liver was extracted and analyzed for crude protein, crude lipid, moisture, ash, carbohydrate contents and fatty acid composition. Results were compared between male and female C. gariepinus and H. nemurus. Liver of female H. nemurus contained the highest amount of ash, crude lipid and carbohydrate and the lowest amount of moisture. Male H. nemurus had the lowest amount of protein, ash and crude lipid content. Moisture was found to be the highest in male C. gariepinus. The main fatty acid content of Asian redtail catfish and African catfish liver were C12:0, C14:0, C15:0, C16:0, C16:1, C17:0, C18:0, C18:1n-9, C182n-6, C183n-3, C204n-6, C24:1, C205n-3, C225n-3, C226n-3. The most abundant fatty acids in both species were oleic acid (18:1n-9) and palmitic acid (16:0). In conclusion, this study showed that H. nemurus and C. gariepinus, are two valuable source of protein and polyunsaturated fatty acid.
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How
to cite this article:
H. Abdi, A. Christianus, E. Ramezani- Fard, C.R. Saad and S.A. Hosseini, 2011. Proximate and Fatty Acid Composition of the Liver of Cultured Asian Redtail Catfish (Hemibagrus nemurus) and African Catfish (Clarias gariepinus). Journal of Fisheries and Aquatic Science, 6: 840-845.
DOI: 10.3923/jfas.2011.840.845
URL: https://scialert.net/abstract/?doi=jfas.2011.840.845
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Received: November 30, 2011;
Accepted: December 21, 2011;
Published: December 30, 2011
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INTRODUCTION
Fish is the primary source of animal protein for an estimated 1/6th of the
worlds population (Adebayo and Popoola, 2008).
Fish consumption and production has been on the rise in Malaysia with consumption
increased from 49 kg per capita in 2000 to 53 kg in 2005 (Farah
et al., 2011) and aquaculture production risen from 170 tons per
capita in 2000 to 210 tons in 2007 (FAO, 2011). Furthermore,
government allocated RM82 million to aid the aquaculture industry (Junaidi
and Hashida, 2010). Catfish is one of the common daily diet among Malaysian
families due to its taste and low market prices. Two species C. gariepinus
and H. nemurus are catfishes highly consumed in Malaysia. In addition
to Malaysia, catfish is an important fish in the aquaculture industry throughout
the world (Mukai and Lim, 2011).
There is a direct relation between production and fish waste. The rise of fish
waste production causes finance waste as well as environmental pollution. The
marine captured fishes total produced almost 25% wastage (Norziah
et al., 2009). The most rejected parts in processing pathway are
skin, head, bones and liver. These discarded parts contained nutritional values
in terms of protein and essential fatty acid compounds that can be used in the
production of fishmeal and fish oil. As a matter of fact, fish oil contained
the most beneficial fatty acids (Celik et al., 2005;
Thammapat et al., 2010) for human such as eicosapentaenoic
acid (EPA), docosahexaenoic acid (DHA) and Arachidonic Acids (AA). Muscle and
liver are two organs involved in the lipids storage (Kandemir
and Polat, 2007). Therefore, consumers demand more choices in the types
of fish oil as population grow. Proximate and fatty acid composition is influenced
by some parameters such as species (Rahnan et al.,
1995; Jabeen and Chaudhry, 2011) and sex (Luzia
et al., 2003; Guil-Guerrero et al., 2011).
For example, fatty acid composition of the liver of winghead shark was totally
different from the liver of sandbar shark (Saify et al.,
2003). In addition, the quality of fatty acid can vary between different
organs (Saify et al., 2003). However, the information
on proximate and fatty acid differences between species and influence of sex
on these parameters are scarce.
MATERIALS AND METHODS Sample preparation: Fish samples were purchased from a wet market (Pasar Borong Selangor, Malaysia) and a fish farm in Semenyih Selangor, Malaysia. Total length and weight were recorded. Livers was extracted and kept at -20°C for further analysis. All samples were prepared in triplicates.
Proximate composition and fatty acid analysis: AOAC methods (AOAC,
2005) were used in all the proximate composition analysis. Fatty Acid Methyl
Ester (FAME) was prepared according to method described by Ramezani-Fard
et al. (2011). Fatty acid methyl ester was then analyzed by a Gas
Chromatography (Agilent 7890N).
Statistical analysis: All data were statistically analyzed by one-way ANOVA method using SPSS 16.0. The mean differences were compared using Duncans multiple range test at p<0.05. RESULTS
Proximate composition: Table 1 shows the liver proximate
composition of H. nemurus and C. gariepinus. There was a significant
difference between two species (p<0.01). Male H. nemurus showed the
lowest amount of protein content comparing the other fish. The highest amount
of ash content among the fish samples belonged to the female H. nemurus
which was followed by C. gariepinus and male H. nemurus.
Table 1: |
Proximate composition (wet weight) of the liver from male
and female of C. gariepinus and H. nemurus |
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All values are in percentage. Standard deviations are given
in parenthesis. Means sharing the same letter do not differ significantly
at p<0.05. (a, b, c, d, e... express statistical differences among mean
values) |
The highest amount of moisture was observed in the liver of male C. gariepinus
followed by female C. gariepinus, male H nemurus and female
H. nemurus. Total fat found to be highest in female H. nemurus followed
by female C. gariepinus, male C. gariepinus and male H. nemurus.
The highest carbohydrate content was observed in female H. nemurus while
the lowest value was observed in male H. nemurus.
Fatty acid composition: Liver fatty acid composition of C. gariepinus and H. nemurus are presented in Table 2. There was significant difference (p<0.01) between fish species and sex in term of fatty acid composition. Monounsaturated fatty acids (MUFAs) were found as the most abundant fatty acids in both species. Male C. gariepinus had the highest amount of 18:1n-9, while the male H. nemurus had the lowest amount of this fatty acid. Female H. nemurus had the highest amount of Saturated Fatty Acid (SFA) and it followed by male H. nemurus and male and female C. gariepinus. Palmitic acid (16:0) was found to be the major SFA. The palmitic acid observed was in female H. nemurus. Stearic acid (18:0) was the second major SFA with the values from 6.71% for female C. gariepinus to 8.80% for male H. nemurus. The omega-6 PUFAs measured in this study were linoleic acid (18:2n-6; 11.12-16.48%), arachidonic acid (20:4n-6; 1.36-4.10%) as well as gamma linolenic acid (18:3n-6; 0.44-1.00%). The 18:2n-6 was the most abundant n-6 PUFA observed in all the fish. Omega-3 PUFAs measured in this study were EPA (20:5n-3; 0.25-0.97%), DPA (22:5n-3; 0.36-0.54%) and DHA (22:6n-3; 1.17-4.17%). The main n-3PUFA was 22:6n-3 which was highest in female H. nemurus (4.17%).
Table 2: |
Fatty acid composition of the liver from male and female
of C. gariepinus and H. nemurus |
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All values are in percentage. Standard deviations are given
in parenthesis. Means sharing the same letter do not differ significantly
at p<0.05. (a, b, c, d, e... express statistical differences among mean
values) |
DISCUSSION
This study showed that proximate and fatty acid composition of liver varies
significantly between H. nemurus and C. gariepinus. In addition,
these results were influenced by sex. Sathivel et al.
(2002) reported a high percentage of moisture (74.9%) and protein (11.4)
in channel catfish (Ictalurus punctatus) but in this study the average
protein was higher (17.26-23.3%). Viscera of Asian catfish (Pangasius bocourti)
had less protein (1%) and more lipid (93.32%) than muscle. These finding suggested
that proximate compositions can varies between organs which is in agreement
with Thammapat et al. (2010). Kandemir
and Polat (2007) reported that liver in rainbow trout (11.2-22.3%) contained
more lipid than muscle (2.20-6.31). Total lipid in liver of wild (32%) and farmed
(37.5%) sea bass (Dicentrarchus. labrax) was reported by Bhouri
et al. (2010). Rainbow trout was estimated between 11.2-22.3% (Kandemir
and Polat, 2007). In contrast, total fat observed in this study was much
less (4.9-12.40%). Hassan et al. (2010) measured
lipid content in wild (3.32-5.91%) and farmed (4.72-7.43%) Catla catla.
This indicated that species has a huge effect on proximate composition of liver.
There was no report on the comparison of liver proximate composition between
sexes. Lipids storage organ varied between species and inactive fishes like
catfish family tend to store lipid in liver more than muscle (Castell
et al., 1972; Kandemir and Polat, 2007).
Therefore, study on the fatty acid composition of liver from these two commonly
consumed species of catfish with a huge amount of wastage during processing
is necessary. Fatty acid composition in the liver was directly affected by species
and sex which is in agreement with Kandemir and Polat (2007).
Approximately 15 fatty acids were found in the liver of H. nemurus and
C. gariepinus. In agreement with Thammapat et
al. (2010), MUFA observed as the most common fatty acids followed by
SFA, n-6 PUFA and n-3 PUFA in both species. Liver in male and female C. gariepinus
stored more n-6 and MUFA compared to male and female H. nemurus. However,
male and female H. nemurus contained more n-3 and SFA. Therefore, the
oil extracted from the liver of H. nemurus showed the characteristic
of having a higher EPA and DHA. Higher n-3 PUFA benefits the heart condition;
therefore, consumption of H. nemurus liver oil is better than C. gariepinus.
The fatty acids C15:0, C16:1 and C24:1 found in this study were not found in
Catla catla (Hassan et al., 2010). However,
pacific halibut (Hippoglossus stenolepsis) had all the above mentioned
fatty acids (Bechtel and Oliveira, 2006). In term of
fatty acid quality, the most common fatty acids in wild sea bass (Bhouri
et al., 2010) and Sardinella lemuru (Khoddami
et al., 2009) is SFA with majority of palmitic acid in Sardinella
and stearic acid in sea bass. However, this study showed that MUFA, oleic acid
in particular, is the most common fatty acids. However both omega-3 and omega-6
were higher in sea bass (D. labrax). In addition, main PUFA class in
sea bass is omega-3. In contrast, this study showed that omega-6 is the main
PUFA class. MUFA was also the main fatty acid compound in Pacific halibut (Hippoglossus
stenolepsis) but overall percentage of omega-3 was also higher than omega-6
(Bechtel and Oliveira, 2006).
Comparing the other catfish species, Shirai et al.
(2001) reported that PUFA is the most abundant fatty acids in the liver
of wild and cultured Silurus asotus while palmitic acid was the highest
fatty acid content in both catfish.
CONCLUSION In conclusion, liver of H. nemurus and C. gariepinus are a valuable sources of protein and lipid with the excellent amount of omega-3, omega-6, MUFA, DHA and EPA that can be used for human consumption instead of being treated as waste.
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REFERENCES |
Farah, A.A., M. Zainalabidin and A.L. Ismail, 2011. The influence of socio-demographic factors and product attributeson attitudes toward purchasing special rice among Malaysian consumers. Int. Food Res. J., 18: 1135-1142. Direct Link |
Adebayo, O.T. and O.M. Popoola, 2008. Comparative evaluation of efficacy and cost of synthetic and non-synthetic hormones for artificial breeding of African catfish ( Clarias gariepinus Burchell, 1822). J. Fish. Aquat. Sci., 3: 66-71. CrossRef | Direct Link |
AOAC, 2005. Official Methods of Analysis. 18th Edn., Association of Analytical Chemists, Washington, DC., USA
Bechtel, P.J. and A.C.M. Oliveira, 2006. Chemical characterization of liver lipid and protein from cold-water fish species. J. Food Sci., 71: S480-S485. CrossRef | Direct Link |
Bhouri, A.M., I. Bouhlel, L. Chouba, M. Hammami, M. El-Cafsi and A. Chaouch, 2010. Total lipid content, fatty acid and mineral compositions of muscles and liver in wild and farmed sea bass ( Dicentrarchus labrax). Afr. J. Food Sci., 4: 522-530. Direct Link |
Castell, J.D., R.O. Sinnhuber, J.H. Wales and D.J. Lee, 1972. Essential fatty acids in the diet of rainbow trout ( Salmo gairdnerii): Growth, feed conversion and some gross deficiency symptoms. J. Nutr., 102: 77-86.
Celik, M., A. Diler and A. Kucukgulmez, 2005. A comparison of the proximate compositions and fatty acid profiles of zander ( Sander lucioperca) from twocdifferent regions and climatic conditions. Food Chem., 92: 637-641.
Ramezani-Fard, E., M.S. Kamarudin, S.A. Harmin and C.R. Saad, 2011. Dietary saturated and omega-3 fatty acids affect growth and fatty acid profiles of Malaysian mahseer. Eur. J. Lipid Sci. Technol., CrossRef |
FAO, 2011. The state of world fisheries and aquaculture. Fisheries and Aquaculture Department, FAO, Rome, Malaysia, http://www.fao.org/fishery/sofia/en.
Guil-Guerrero, J.L., E. Venegas-Venegas, M.A. Rincon-Cervera and M.D. Suarez, 2011. Fatty acid profiles of livers from selected marine fish species. J. Food Compos. Anal., 24: 217-222. CrossRef |
Hassan, M., S.A.S. Chatha, I. Tahira and B. Hussain, 2010. Total lipids and fatty acid profile in the liver of wild and farmed catla catla fish. Grasas Aceites, 61: 52-57. CrossRef | Direct Link |
Jabeen, F. and A.S. Chaudhry, 2011. Chemical compositions and fatty acid profiles of three freshwater fish species. Food Chem., 125: 991-996. CrossRef | Direct Link |
Junaidi, M.S. and N.H. Hashida, 2010. Effect of pH on the waste production of catfish in running water system. Centre For Foundation Studies in Science, University of Malaya, 50603 Kuala Lumpur, Malaysia, http://www.seafdec.org.my/v12/images/pdf/afas2010/FP1.pdf.
Kandemir, S. and N. Polat, 2007. Seasonal variation of total lipid and total fatty acid in muscle and liver of rainbow trout ( Oncorhynchus mykiss W., 1792) reared in derbent dam lake. Turk. J. Fish. Aquat. Sci., 7: 27-31. Direct Link |
Khoddami, A., A.A. Ariffin, J. Bakar and H.M. Ghazali, 2009. Fatty acid profile of the oil extracted from fish waste (head, intestine and liver) ( Sardinella lemuru). World Applied Sci. J., 7: 127-131. Direct Link |
Mukai, Y. and L.S. Lim, 2011. Larval rearing and feeding behavior of African catfish, Clarias gariepinus under dark conditions. J. Fish. Aquat. Sci., 6: 272-278. CrossRef | Direct Link |
Norziah, M.H., J. Nuraini and K.Y. Lee, 2009. Studies on the extraction and characterization of fish oil from wastes of seafood processing industry. Asian J. Food Agro-Ind., 2: 959-973. Direct Link |
Luzia, L.A., G.R. Sampaio, C.M.N. Castellucci and E.A.F.S. Torres, 2003. The influence of season on the lipid profiles of five commercially important species of Brazilian fish. Food Chem., 83: 93-97. CrossRef |
Rahnan, S.A., T.S. Huah, O. Nassan and N.M. Daud, 1995. Fatty acid composition of some Malaysian freshwater fish. Food Chem., 54: 45-49. CrossRef |
Saify, Z.S., S. Akhtar, K.M. Khan, S. Perveen, S.A.M. Ayattollahi. S. Siddiqui and M.Z. Khan, 2003. Study on the fatty acid composition of fish liver oil from two marine fish, Eusphyra blochii and Carcharhinus bleekeri. Turk. J. Chem., 27: 251-258. Direct Link |
Sathivel, S., W. Prinyawiwatkul, C.C. Grimm, J.M. King and S. Lloyd, 2002. FA composition of crude oil recovered from catfish viscera. J. Am. Oil Chem. Soc., 79: 989-992. Direct Link |
Shirai, N., H. Suzuki, S. Tokairin and S. Wada, 2001. Spawning and season affect lipid content and fatty acid composition of ovary and liver in Japanese catfish ( Silurus asotus). Comp. Biochem. Physiol., 129B: 185-195. CrossRef |
Thammapat, P., P. Raviyan and S. Siriamornpun, 2010. Proximate and fatty acids composition of the muscles and viscera of Asian catfish ( Pangasius bocourti). Food Chem., 122: 223-227. CrossRef |
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