Orientador: Carlos Raimundo Ferreira Grosso / Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos / Made available in DSpace on 2018-08-11T10:29:59Z (GMT). No. of bitstreams: 1 Bueno_CamilaMoraisMarques_M.pdf: 1235801 bytes, checksum: 01bf63d6c99cca84c0ff1402a773967a (MD5) Previous issue date: 2008 / Resumo: Dois grandes desafios na cadeia produtiva da piscicultura são o aproveitamento dos subprodutos gerados durante o processamento do pescado e a produção de micropartículas que sejam mais atrativas para a alimentação de larvas de peixes. O objetivo do trabalho foi extrair e caracterizar gelatina de pele de tilápia para utilizá-la como um substituto das gelatinas de mamíferos na formação da parede, juntamente com goma arábica, de micropartículas obtidas por coacervação complexa contendo como recheio o óleo de salmão. Gelatina de pele de tilápia foi obtida e caracterizada e comparada com gelatina suína comercial quanto à força de gel (Dnqqo), perfil de textura, ponto de fusão, distribuição de massa molar e composição centesimal. Foram também avaliadas as condições de processamento das micropartículas, sua morfologia e microestrutura por microscopia óptica e eletrônica de varredura, diâmetro médio e eficiência de encapsulação. Os resultados de força de gel para gelatina suína e de peixe do segundo lote produzido foram bastante similares, apresentando valores de 192,2 ± 2,9 g e de 202,8 ± 3,7 g, respectivamente. O primeiro lote de gelatina de peixe apresentou valor de força de gel bem inferior em relação ao segundo lote (11,5 ± 0,7 g), devido à presença de um conteúdo lipídico relativamente maior no primeiro lote. A gelatina suína apresentou ponto inicial de fusão maior (27,5°C) que as gelatinas de peixe do primeiro e do segundo lotes (18,5°C e 24,0°C, respectivamente). Quanto à distribuição de massa molar, observou-se maior degradação na gelatina suína do que nas gelatinas de peixe. O aumento da velocidade de agitação (14000 rpm) produziu micropartículas com recheio constituído por gotículas menores de óleo. O aumento da concentração de polímeros de parede (5,0 e 7,5%) resultou na produção de partículas com formatos irregulares. As diferentes gelatinas utilizadas para formação das paredes das micropartículas não provocaram alterações significativas nas eficiências de encapsulação, com os valores variando de 59,7 a 72,4%. Os diâmetros médios das micropartículas produzidas com as diferentes gelatinas e com os diferentes recheios variaram de 83 a 150 µm. A utilização de óleo de salmão e gelatina de peixe não modificou a morfologia das micropartículas, que mantiveram a esfericidade característica e a integridade das paredes. Considerando os resultados obtidos, conclui-se que é possível substituir gelatina suína comercial por gelatina de pele de tilápia e oleoresina de páprica + óleo de soja por óleo de salmão, permitindo uma produção de micropartículas ricas em ômega 3 e com uma possível maior atratividade na alimentação de larvas de peixes / Abstract: Two great challenges in the pisciculture production chain are the use of by-products generated during the fish processing and the production of more attractive microparticles for fish larvae feeding. The aim of this work was to extract and to characterize gelatin from tilapia skin to use it as a substitute of mammalian gelatins in the formation of matrix of microparticles, obtained by complex coacervation, containing salmon oil. Tilapia skin gelatin was obtained, characterized and compared to commercial pig gelatin as for gel strength (Dnqqo), texture profile, melting point, molecular weight distribution and proximate composition. Conditions of microparticles processing were also evaluated, their morphology and microstructure by optical and scanning electron microscope, mean diameter and encapsulation efficiency. Pig gelatin and one second lot of fish gelatin exhibited quite similar results of gel strength with values of 192,2 ± 2,9 g and 202,8 ± 3,7 g, respectively. Gel strength of first lot of fish gelatin (11,5 ± 0,7 g) was smaller than the second lot due to the lipid content slightly larger in the first lot. Pig gelatin presented an initial melting point larger (27,5°C) than first and second lots of fish gelatins (18,5°C and 24,0° C, respectively). Related to the molecular weight distribution, more degradation was observed in pig gelatin than fish gelatin. Higher agitation speed (14000 rpm) produced microparticles with core material constituted by smaller droplets of oil. The increase of the concentration of matrix polymeric material (5,0 and 7,5%) resulted in production of particles with irregular formats. The different gelatins used as matrix of microparticles did not cause significant alterations in the efficiencies of encapsulation, with values varying from 59,7 to 72,4%, as well as, the replacement of oleoresin of paprika + soy oil for salmon oil also did not produced significant differences among the microparticles regarding to this parameter. The mean diameter remained between 83 and 150 µm considering all the particles produced. The application of salmon oil and fish gelatin did not impair the morphology of microparticles that kept the characteristic spherical format and the wall integrity. Considering the obtained results, it is possible to substitute commercial pig gelatin for tilapia skin gelatin and oleoresin of paprika + soybean oil for salmon oil, allowing a production of microparticles rich in ômega 3 oil and possibly with a greater attractiveness in the feeding of fish larvae / Mestrado / Nutrição Experimental e Aplicada à Tecnologia de Alimentos / Mestre em Alimentos e Nutrição

La fonctionnalisation d'emballages biodégradables avec des antioxydants naturels est l'une des techniques prometteuses pour améliorer la conservation des aliments, diminuer la quantité de conservateurs chimiques utilises, protéger la dégradation aromatique des produits et ainsi conserver une meilleure qualité globale. Le contrôle du relargage de ces composés actifs de l'emballage vers l'aliment permet d'étendre l'efficacité de la fonctionnalisation en libérant progressivement les antioxydants à la surface de l'aliment. L'objectif global de ce travail était de fonctionnaliser le polymère HPMC afin de produire un film d'emballage coloré à activité antioxydante et d'évaluer son aptitude à servir d'emballage actif. Tout d'abord, des films d'HPMC contenant différents colorants synthétiques comme le bleu, le vert, le jaune, le rouge et le blanc ont été testés afin de déterminer la couleur la plus adaptée pour le contrôle de la photo-oxydation de produits gras. Ensuite, la couleur rouge synthétique, montrant un maximum de contrôle contre la photo-oxydation, a été remplacée par des composés actifs naturels de même couleur. Ces composés provenaient soit d'un mélange d'extraits de betterave et de carottes pourpres, d'un mélange de bétalaïnes soit d'un mélange d'anthocyanes. Le mode d'incorporation de ces composés actifs dans la matrice d'HPMC, leurs effets sur les propriétés thermiques, mécaniques, barrière et structurales des films ont été étudiés. Les résultats ont montré que l'intégration de ces différents composés actifs naturels a permis d'améliorer les propriétés des films. Les composés actifs utilisés ont la capacité de contrôler le photo-vieillissement de la matrice polymérique et que l'HPMC est un bon candidat pour incorporer ces molécules et permettre le contrôle de la dégradation de produits alimentaires riches en lipides / Biodegradable packaging functionalized with natural antioxidants is one of the promising techniques to enhance foods shelf-life, lower use of preservatives in food formations, higher protection of flavours and higher food qualities. Controlled release of these bioactive compounds from packaging to food surface provides longer food stability by continuously librating antioxidants at food surface. The overall objective of the present work was to functionalize the HPMC polymer as colored antioxidant packaging and investigate its suitability as active packaging for unsaturated lipids. Firstly, HPMC films containing different synthetic colours like blue, green, yellow, red and white were tested to chose a suitable color having control against photo-oxidation. Secondly, red synthetic color (showing maximum control against pho-oxidation) was replaced by natural active red compounds including "natural red color" (beetroot extract + purple carrot extract), betalains and anthocyanins to produce bioactive food packaging. Mode of incorporation of these active compounds in HPMC matrix and also their potential effects on thermal, mechanical, barrier and structural properties of films were investigated. Controlled release kinetics, antioxidant capacity and light stability of bioactive compounds in HPMC films were also investigated. The overall results showed that successful incorporation of different natural active compounds have capability to improve film properties. The active compounds under discussion have ability to control photo ageing of polymer matrix and HPMC has the capability for being a suitable carrier for antioxidant active packaging for some food products

Três experimentos foram conduzidos para determinar o efeito de fontes lipídicas nos desempenhos reprodutivo e zootécnico de lambaris e a comparação no perfil de ácidos graxos nos tecidos de lambaris selvagens e de cativeiro. Para o experimento de reprodução e de crescimento foram fornecidas, desde a fase larval até o período reprodutivo (11 meses), três dietas elaboradas com diferentes fontes de óleo: soja (SO); óleo de resíduos de tilápia (TI); óleo de resíduo de salmão (SA). No período reprodutivo, os peixes (36 fêmeas e 72 machos) foram induzidos à desova artificialmente e foram avaliados os parâmetros reprodutivos (volume e número total de ovos, taxas de fertilização e eclosão, diâmetro do ovo e comprimento da larva), bem como, o acompanhamento da regeneração ovocitária pós-desova. Observaram-se ovos e larvas maiores e taxas de fertilização superiores na progênie dos peixes alimentados com dietas contendo óleo de peixe, o que pode estar relacionado aos maiores valores da relação n-3/n-6 encontrados nos ovos. Para o experimento de desempenho zootécnico foram utilizados 192 lambaris sexados (espículas na nadadeira anal do macho), sendo 120 machos (peso médio 2,58 ± 0,13g) e 72 fêmeas (peso médio 4,00 ± 0,09g). O Delineamento utilizado foi o Inteiramente Casualizado em Esquema Fatorial 3 x 2, composto por três dietas (SO, TI, SA) e dois sexos. Verificou-se que as fêmeas apresentaram maior ganho em peso, taxas de conversão alimentar e taxa de eficiência protéica mais satisfatórias quando comparados com os machos, os quais apresentaram maior sobrevivência no final do experimento, independente da dieta fornecida. Para o terceiro experimento foram coletados 30 lambaris fêmeas selvagens e 30 fêmeas provenientes do cultivo. Extraíram-se os lipídios dos tecidos (músculo, ovários e fígado) de cada grupo, os quais foram separados (fases apolar e polar) e determinados os perfis de ácidos graxos. Os resultados foram submetidos a ANOVA e diferenciados pelo teste F. Os lambaris de ambos os grupos apresentaram em média 3,5g.100g-1 de teor de gordura no músculo. Os ovários dos peixes selvagens apresentaram a maior concentração de lipídios (14,447g.100g-1) quando comparados com os de cativeiro (13,181g.100g-1). A dieta não conseguiu suprir a quantidade mínima de importantes ácidos graxos no lipídio total e frações dos tecidos das fêmeas provenientes do cultivo em relação às selvagens. O ácido linolênico, considerado essencial para peixes de água doce, esteve presente em menores quantidades no lipídio total e nas frações polar e apolar nos tecidos dos lambaris cultivados, o que pode estar relacionado com deficiência em dietas comerciais para peixes onívoros. Com base nos resultados observados nos experimentos de reprodução e desempenho, sugere-se a inclusão de óleo de resíduos de tilápia e salmão na ração de peixes de lambaris. Ainda foi observado que os lambaris são capazes de elongar e dessaturar os ácidos graxos com 18 carbonos na cadeia, para a produção de Ácidos Araquidônico (AA), Eicosapentaenóico (EPA) e Docosahexaenóico (DHA), devido às baixas quantidades desses ácidos graxos na dieta e posterior aumento nos tecidos. / Three trials were conducted to determine the effect of lipid sources on lambari reproductive and growth performances as well as to make the comparison in the fatty acid profiles in tissues of lambari wild and captive. For the reproduction and growth performances were provided since the larval stage until the reproductive period (11 months), three diets containing different sources of oil: soybean oil (SO); tilapia waste oil (IT); salmon waste oil ( SA). During the reproductive period, fish (36 females and 72 males) were artificially induced to spawn and the reproduction parameters (volume and total number of eggs, fertilization and hatching rates, egg diameter and larval length) were evaluated, as well as monitoring of oocyte regeneration post-spawning. It were observed larger eggs and larvae and higher fertilization rate in the progeny of fish fed diets containing fish oil, which may be related to higher n-3/n-6 ratio values found in the eggs. For the trial of growth performance were used 192 sexed lambaris (male anal fin spines) with 120 males (mean weight 2.58 ± 0.13g) and 72 females (mean weight 4.00 ± 0.09g). The fish were separated on a random method in a factorial scheme 3 x 2, composed by three diets (SO, TI e SA) and two sexes. It was verified that females had higher weight gain, improved feed conversion and protein efficiency rates than males, which showed higher survival at the end of the trial, regardless of diet. In the third trial were collected 30 wild and 30 captive females. The lipids of tissues (muscle, liver and ovary) were extracted from each group and were separated (polar and non polar) and thus determined the fatty acids profiles. The results were analyzed by ANOVA and F test. The lambaris of both groups had mean of 3.5g.100g-1 in the muscle and the wild fish ovaries showed the highest concentration of lipids (14.447g.100g-1) than farming fish (13.181 g.100g-1). The diet failed to supply the minimum amount of important fatty acids in fractions and total lipids of cultivate females and these evidences were higher in the ovaries. Linolenic acid which is considered essential for freshwater fish, was present in smaller amounts in total lipids and polar and nonpolar fractions in all tissues of the cultivated lambari, which may be related to default in commercial diets for omnivores fish. In view of parameters observed in reproduction and growth trials, it can be suggest the inclusion of waste tilapia and salmon oil in lambari broodstock diet. Also it was observed that lambaris have the capacity elongation and desaturation of fatty acids with 18 carbons in the chain for the Arachidonic Acid (AA), Eicosapentaenoic Acid (EPA) and Docosahexaenoic Acid (DHA) production due to low amount of these fatty acids in the diet and the increase in the tissues.

Salmon is a good source of long chain (LC) omega 3 fatty acids and selenium; these are well recognised for their health benefits. Recommendations for LC omega 3 fatty acid intakes presume equivalence between fish and fish oil. The aim of this research was to compare the effects of consuming salmon with salmon oil capsules on LC omega 3 fatty acid and selenium status. Forty four healthy subjects were randomly assigned to consume either two servings of 120 g farmed New Zealand King (FNZK) salmon/week or 2, 4 or 6 capsules of salmon oil/day for 8 weeks. Fasting blood samples, anthropometric measures, food consumption habits information and blood pressure (BP) measurements were obtained at the study commencement and ending. Each subject’s intake of LC omega 3 fatty acids and selenium was determined by analysing the fatty acid and selenium content of duplicate portions of cooked salmon and capsules. The amount of salmon consumed was then calculated by subtracting unconsumed amounts of salmon and then calculating the intake of LC omega 3 fatty acids as grams of LC omega 3 fatty acids consumed per day. Percentage of compliance to capsule intake, based on counts of unconsumed capsules, was calculated to determine the amount of LC omega 3 fatty acids consumed per day from capsules. Change in red blood cells (RBC) LC omega 3 fatty acid levels from equivalent amounts of LC omega 3 fatty acids consumed from capsules and salmon were compared using linear regression analysis predictive models fitted to the capsule data. Omega 3 index was calculated. LC omega 3 fatty acid intakes from salmon and 2, 4 and 6 capsules were 0.82, 0.24, 0.47 and 0.68 g/day, respectively. Equal amounts of LC omega 3 fatty acids consumed from salmon and capsules resulted in similar increases in RBC LC omega 3 fatty acids and omega 3 index (RBC eicosapentaenoic acid (EPA): 0.80 [0.58 – 1.02] vs. 1.00 [0.71 – 1.27] %; RBC docosahexaenoic acid (DHA): 0.93 [0.58 – 1.29] vs. 0.99 [0.68 – 1.31] %; omega 3 index: 1.92 [1.46 – 2.38] vs. 2.25 [1.65 – 2.83] %). The capsules did not contain selenium, but the salmon provided 6.84 µg selenium/day. Plasma selenium concentrations increased significantly in the salmon group compared to the capsule

Salmon is a good source of long chain (LC) omega 3 fatty acids and selenium; these are well recognised for their health benefits. Recommendations for LC omega 3 fatty acid intakes presume equivalence between fish and fish oil. The aim of this research was to compare the effects of consuming salmon with salmon oil capsules on LC omega 3 fatty acid and selenium status. Forty four healthy subjects were randomly assigned to consume either two servings of 120 g farmed New Zealand King (FNZK) salmon/week or 2, 4 or 6 capsules of salmon oil/day for 8 weeks. Fasting blood samples, anthropometric measures, food consumption habits information and blood pressure (BP) measurements were obtained at the study commencement and ending. Each subject’s intake of LC omega 3 fatty acids and selenium was determined by analysing the fatty acid and selenium content of duplicate portions of cooked salmon and capsules. The amount of salmon consumed was then calculated by subtracting unconsumed amounts of salmon and then calculating the intake of LC omega 3 fatty acids as grams of LC omega 3 fatty acids consumed per day. Percentage of compliance to capsule intake, based on counts of unconsumed capsules, was calculated to determine the amount of LC omega 3 fatty acids consumed per day from capsules. Change in red blood cells (RBC) LC omega 3 fatty acid levels from equivalent amounts of LC omega 3 fatty acids consumed from capsules and salmon were compared using linear regression analysis predictive models fitted to the capsule data. Omega 3 index was calculated. LC omega 3 fatty acid intakes from salmon and 2, 4 and 6 capsules were 0.82, 0.24, 0.47 and 0.68 g/day, respectively. Equal amounts of LC omega 3 fatty acids consumed from salmon and capsules resulted in similar increases in RBC LC omega 3 fatty acids and omega 3 index (RBC eicosapentaenoic acid (EPA): 0.80 [0.58 – 1.02] vs. 1.00 [0.71 – 1.27] %; RBC docosahexaenoic acid (DHA): 0.93 [0.58 – 1.29] vs. 0.99 [0.68 – 1.31] %; omega 3 index: 1.92 [1.46 – 2.38] vs. 2.25 [1.65 – 2.83] %). The capsules did not contain selenium, but the salmon provided 6.84 µg selenium/day. Plasma selenium concentrations increased significantly in the salmon group compared to the capsule

Salmon is a good source of long chain (LC) omega 3 fatty acids and selenium; these are well recognised for their health benefits. Recommendations for LC omega 3 fatty acid intakes presume equivalence between fish and fish oil. The aim of this research was to compare the effects of consuming salmon with salmon oil capsules on LC omega 3 fatty acid and selenium status. Forty four healthy subjects were randomly assigned to consume either two servings of 120 g farmed New Zealand King (FNZK) salmon/week or 2, 4 or 6 capsules of salmon oil/day for 8 weeks. Fasting blood samples, anthropometric measures, food consumption habits information and blood pressure (BP) measurements were obtained at the study commencement and ending. Each subject’s intake of LC omega 3 fatty acids and selenium was determined by analysing the fatty acid and selenium content of duplicate portions of cooked salmon and capsules. The amount of salmon consumed was then calculated by subtracting unconsumed amounts of salmon and then calculating the intake of LC omega 3 fatty acids as grams of LC omega 3 fatty acids consumed per day. Percentage of compliance to capsule intake, based on counts of unconsumed capsules, was calculated to determine the amount of LC omega 3 fatty acids consumed per day from capsules. Change in red blood cells (RBC) LC omega 3 fatty acid levels from equivalent amounts of LC omega 3 fatty acids consumed from capsules and salmon were compared using linear regression analysis predictive models fitted to the capsule data. Omega 3 index was calculated. LC omega 3 fatty acid intakes from salmon and 2, 4 and 6 capsules were 0.82, 0.24, 0.47 and 0.68 g/day, respectively. Equal amounts of LC omega 3 fatty acids consumed from salmon and capsules resulted in similar increases in RBC LC omega 3 fatty acids and omega 3 index (RBC eicosapentaenoic acid (EPA): 0.80 [0.58 – 1.02] vs. 1.00 [0.71 – 1.27] %; RBC docosahexaenoic acid (DHA): 0.93 [0.58 – 1.29] vs. 0.99 [0.68 – 1.31] %; omega 3 index: 1.92 [1.46 – 2.38] vs. 2.25 [1.65 – 2.83] %). The capsules did not contain selenium, but the salmon provided 6.84 µg selenium/day. Plasma selenium concentrations increased significantly in the salmon group compared to the capsule

Três experimentos foram conduzidos para determinar o efeito de fontes lipídicas nos desempenhos reprodutivo e zootécnico de lambaris e a comparação no perfil de ácidos graxos nos tecidos de lambaris selvagens e de cativeiro. Para o experimento de reprodução e de crescimento foram fornecidas, desde a fase larval até o período reprodutivo (11 meses), três dietas elaboradas com diferentes fontes de óleo: soja (SO); óleo de resíduos de tilápia (TI); óleo de resíduo de salmão (SA). No período reprodutivo, os peixes (36 fêmeas e 72 machos) foram induzidos à desova artificialmente e foram avaliados os parâmetros reprodutivos (volume e número total de ovos, taxas de fertilização e eclosão, diâmetro do ovo e comprimento da larva), bem como, o acompanhamento da regeneração ovocitária pós-desova. Observaram-se ovos e larvas maiores e taxas de fertilização superiores na progênie dos peixes alimentados com dietas contendo óleo de peixe, o que pode estar relacionado aos maiores valores da relação n-3/n-6 encontrados nos ovos. Para o experimento de desempenho zootécnico foram utilizados 192 lambaris sexados (espículas na nadadeira anal do macho), sendo 120 machos (peso médio 2,58 ± 0,13g) e 72 fêmeas (peso médio 4,00 ± 0,09g). O Delineamento utilizado foi o Inteiramente Casualizado em Esquema Fatorial 3 x 2, composto por três dietas (SO, TI, SA) e dois sexos. Verificou-se que as fêmeas apresentaram maior ganho em peso, taxas de conversão alimentar e taxa de eficiência protéica mais satisfatórias quando comparados com os machos, os quais apresentaram maior sobrevivência no final do experimento, independente da dieta fornecida. Para o terceiro experimento foram coletados 30 lambaris fêmeas selvagens e 30 fêmeas provenientes do cultivo. Extraíram-se os lipídios dos tecidos (músculo, ovários e fígado) de cada grupo, os quais foram separados (fases apolar e polar) e determinados os perfis de ácidos graxos. Os resultados foram submetidos a ANOVA e diferenciados pelo teste F. Os lambaris de ambos os grupos apresentaram em média 3,5g.100g-1 de teor de gordura no músculo. Os ovários dos peixes selvagens apresentaram a maior concentração de lipídios (14,447g.100g-1) quando comparados com os de cativeiro (13,181g.100g-1). A dieta não conseguiu suprir a quantidade mínima de importantes ácidos graxos no lipídio total e frações dos tecidos das fêmeas provenientes do cultivo em relação às selvagens. O ácido linolênico, considerado essencial para peixes de água doce, esteve presente em menores quantidades no lipídio total e nas frações polar e apolar nos tecidos dos lambaris cultivados, o que pode estar relacionado com deficiência em dietas comerciais para peixes onívoros. Com base nos resultados observados nos experimentos de reprodução e desempenho, sugere-se a inclusão de óleo de resíduos de tilápia e salmão na ração de peixes de lambaris. Ainda foi observado que os lambaris são capazes de elongar e dessaturar os ácidos graxos com 18 carbonos na cadeia, para a produção de Ácidos Araquidônico (AA), Eicosapentaenóico (EPA) e Docosahexaenóico (DHA), devido às baixas quantidades desses ácidos graxos na dieta e posterior aumento nos tecidos. / Three trials were conducted to determine the effect of lipid sources on lambari reproductive and growth performances as well as to make the comparison in the fatty acid profiles in tissues of lambari wild and captive. For the reproduction and growth performances were provided since the larval stage until the reproductive period (11 months), three diets containing different sources of oil: soybean oil (SO); tilapia waste oil (IT); salmon waste oil ( SA). During the reproductive period, fish (36 females and 72 males) were artificially induced to spawn and the reproduction parameters (volume and total number of eggs, fertilization and hatching rates, egg diameter and larval length) were evaluated, as well as monitoring of oocyte regeneration post-spawning. It were observed larger eggs and larvae and higher fertilization rate in the progeny of fish fed diets containing fish oil, which may be related to higher n-3/n-6 ratio values found in the eggs. For the trial of growth performance were used 192 sexed lambaris (male anal fin spines) with 120 males (mean weight 2.58 ± 0.13g) and 72 females (mean weight 4.00 ± 0.09g). The fish were separated on a random method in a factorial scheme 3 x 2, composed by three diets (SO, TI e SA) and two sexes. It was verified that females had higher weight gain, improved feed conversion and protein efficiency rates than males, which showed higher survival at the end of the trial, regardless of diet. In the third trial were collected 30 wild and 30 captive females. The lipids of tissues (muscle, liver and ovary) were extracted from each group and were separated (polar and non polar) and thus determined the fatty acids profiles. The results were analyzed by ANOVA and F test. The lambaris of both groups had mean of 3.5g.100g-1 in the muscle and the wild fish ovaries showed the highest concentration of lipids (14.447g.100g-1) than farming fish (13.181 g.100g-1). The diet failed to supply the minimum amount of important fatty acids in fractions and total lipids of cultivate females and these evidences were higher in the ovaries. Linolenic acid which is considered essential for freshwater fish, was present in smaller amounts in total lipids and polar and nonpolar fractions in all tissues of the cultivated lambari, which may be related to default in commercial diets for omnivores fish. In view of parameters observed in reproduction and growth trials, it can be suggest the inclusion of waste tilapia and salmon oil in lambari broodstock diet. Also it was observed that lambaris have the capacity elongation and desaturation of fatty acids with 18 carbons in the chain for the Arachidonic Acid (AA), Eicosapentaenoic Acid (EPA) and Docosahexaenoic Acid (DHA) production due to low amount of these fatty acids in the diet and the increase in the tissues.