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Different feeding habits influence the activity of digestive enzymes in freshwater fish/Diferentes habitos alimentares influenciam a atividade das enzimas digestivas em peixes de agua doce.

INTRODUCTION

Fish usually exhibit high versatility in their feeding habits that is reflected in different anatomical and functional features. This allows fish to explore a wide range of food resources and maximize the use of available food in the environment (PERETTI & ADRIAN, 2008). The digestive potential of fish is highly variable, changing with species, age, size, food and feeding history, stage of maturity and temperature (GARCIA-CARRENO et al., 2002). The analysis of digestive enzymes provides information on fish nutritional physiology and on their ability to take advantage of the different nutritional fractions of the feed (TENGJAROENKUL et al., 2000; ODEDEYI & FAGBENRO, 2010; LAZZARI et al., 2010; 2015).

Ctenopharyngodon idella (grass carp) (Characiformes, Cyprinidae), is an herbivorous fish species that feeds on aquatic plants (BILLARD & BERNI, 2004). The omnivorous Leporinus obtusidens (piava) (Characiformes, Anostomidae) feed on plants, insects and fishes (REYNALTE-TATAJE & ZANIBONIFILHO, 2010; LAZZARI et al., 2015). Rhamdia quelen (silver catfish) (Siluriformes, Heptapteridae) is an omnivorous fish with a tendency towards ichthyophagy, depending on food availability in the environment (BALDISSEROTTO et al., 2013). Hoplias malabaricus (traira) (Characiformes, Erythrinidae) is a carnivorous fish species that, in the adult stage, ingests intact preys (MENIN & MIMURA, 1991).

Several studies of digestive enzymes in fish species with different feeding habits have been reported (KUZ'MINA & KUZ'MINA, 1990; CHAKRABARTI et al., 2006; LOPEZ-VASQUEZ et al., 2009) and some showed that fish growth might be related to digestive enzyme capacity (CHAKRABARTI et al., 2006; FILIPPOV et al., 2013; LAZZARI et al., 2015). The aim of this study was to investigate protease and carbohydrase activities in four fish species raised in Brazil. The major propose is collected information concerning fish cultivated in Southern Brazil for improved in the future fish diets according to digestive enzymatic profile.

MATERIALS AND METHODS

Ten individuals of each species, C. idella (20.46 [+ or -] 3.9g and 12.95 [+ or -] 1.7cm), R. quelen (66.20 [+ or -] 10.5g and 18.75 [+ or -] 1.5cm) and L. obtusidens (69.80 [+ or -] 11.7g and 25.41 [+ or -] 0.8cm) with approximate age were obtained from the fish culture sector at Universidade Federal de Santa Maria. Hoplias malabaricus (60.30 [+ or -] 10.9g and 16.64 [+ or -] 1.6cm) was obtained from regional pond producer. Both species were fasted for 12h before euthanasia by section of spinal cord. Body weight and length were taken subsequently.

The fish were kept in 250L tanks with proper charge density for each species, and water quality parameters were monitored regularly: dissolved oxygen (5.8 [+ or -] 0.6mg [L.sup.-1]); temperature (23 [+ or -] 0.4 [degrees]C, using an oxygen meter Y5512; YSI Inc., Yellow Springs, OH, USA); pH 7.5 [+ or -] 0.3 (DMPH-2 pH meter, Digimed, Sao Paulo, SP, Brazil); total ammonia nitrogen levels (0.14 [+ or -] 0.04mg [L.sup.-1]) (EATON et al., 2005); un-ionized ammonia (N[H.sub.3]) levels 0.007 [+ or -] 0.001mg [L.sup.-1] (COLT, 2002); alkalinity (42 [+ or -] 2.7mg [L.sup.-1] CaC[O.sub.3]); nitrite (0.0033 [+ or -] 0.003mg [L.sup.-1]) (BOYD & TUCKER, 1992) and; water hardness (26.0 [+ or -] 1.4mg [L.sup.-1] CaC[O.sub.3]) (EDTA titrimetric method).

The digestive tract was immediately removed after euthanasia and divided into four sections: stomach (except for the grass carp, which does not possess stomach), anterior (or pyloric ceca), mid and posterior intestines. Portions were placed into ice and then stored at -20[degrees]C. Tissues were homogenized in buffer solution containing phosphate (10mM) and Tris (20mM), pH 7.0 using a Potter-Elvehijen homogenizer. The homogenates were centrifuged at 10.000g for 10min at 4[degrees]C and the supernatant (crude extract) was used as an enzyme source for all assays.

The effect of different pH on the incubation medium was studied for protease alkaline and amylase activities. Total acid protease activity was measured in the stomach, using a non-specific substrate (casein 1.5%) according to HIDALGO et al. (1999).

Trypsin, chymotrypsin, amylase and maltase were determined in homogenates from the stomach and anterior, mid and posterior intestine. The experimental protocol was modified according to BERNFELD (1955). The starch hydrolyzed by the enzyme and glucose levels were determined according to PARK & JOHNSON (1949). The protein content of crude extracts was determined by the method of LOWRY et al. (1951), using bovine serum albumin as a standard. For more details, see the technical of study LAZZARI et al. (2010).

Differences between species were analyzed by one-way analysis of variance followed by the Duncan test (Statistica 5.0). Data were expressed as mean [+ or -] SEM, and differences were considered significant at a probability level of 95% (P<0.05).

RESULTS

Trypsin, chymotrypsin and maltase activities were observed in the stomach of R. quelen, L. obtusidens, and H. malabaricus. The greatest trypsin activity was found in H. malabaricus following for L. obtusidens. The low values for trypsin were recorded to R. quelen. Chymotrypsin activity in the stomach was similar to R. quelen and H. malabaricus, and L. obtusidens showed lower activity as compared to other fish species. Maltase activity was highest in L. obtusidens comparing to H. malabaricus and R. quelen that showed similar maltase activity in stomach (Table 1).

Ctenopharyngodon idella and L. obtusidens showed the highest amylase activity at pH 7.0 and H. malabaricus at pH 8.5 and pH 8.0 in the anterior and midintestine, respectively (Figure 1A and B). Rhamdia quelen showed highest activity at pH 7.0 in the middle intestine (Figure 1B). Higher amylase activity in the anterior and mid in C. idella (Figure 1A and B). In the stomach the highest amylase activity was observed at pH 7.0 for L. obtusidens and R. quelen and pH 8.0 for H. malabaricus (Figure 1C).

Alkaline protease presented the highest activities at pH 8.0 or 8.5 for all species, but R. quelen and H. malabaricus also showed high activities at pH 9.0 and 10.0. Compared to the other species, C. idella continued to show high activity of alkaline protease in the middle portion of the intestine (Figure 2A and B). The highest acid protease activity in the stomach was at pH 2.5 for H. malabaricus and L. obtusidens and pH 2.0 for R. quelen (Figure 2C). In C. idella the mid intestine showed the highest activity for amylase and maltase when compared to anterior and posterior segments. In R. quelen the highest activity of these enzymes was exhibited in the anterior intestine. In L. obtusidens the highest amylase activity was detected in the anterior intestine and maltase in the mid intestine, but H. malabaricus showed very low amylase activity in all intestine portions. On the other hand, H. malabaricus presented maltase activity in middle and posterior intestine portions similar to that obtained for R. quelen, but lower than L. obtusidens and C. idella. (Figure 3).

The highest trypsin activity was observed in all intestine portions of H. malabaricus. Ctenopharyngodon idella exhibited the highest trypsin activity in the anterior intestine, L. obtusidens in the mid intestine and R quelen in the posterior intestine (Figure 3C). Ctenopharyngodon idella showed the highest chymotrypsin activity at all intestine portions. Rhamdia quelen and H. malabaricus showed high activity of this enzyme in the anterior portion but for L. obtusidens the highest activity was observed in the posterior intestine (Figure 3D).

DISCUSSION

The knowledge of the feeding habits of different fish species associated with enzymes activities in the digestive tract is important to provide an appropriate diet for each species because digestive enzymes activity very reflects the changes in dietary (PERETTI & ANDRIAN, 2008; LAZZARI et al., 2010; 2015).

The carnivorous H. malabaricus showed lower amylase, maltase, alkaline protease and chymotrypsin activity compared to the other fish species studied. The main digestive enzymes of H. malabaricus are represented by acid protease in the stomach and trypsin in the intestine, but this species also showed some chymotrypsin and maltase activity in the stomach and all intestine portions. Other carnivorous species such as Oncorhynchus mykiss and Pseudoplatystoma corruscans also showed high protease activity in the stomach (HIDALGO et al., 1999; LUNDSTEDT et al., 2004). In the present study, amylase and maltase activities were found in H. malabaricus, likely because they would be required to digest the glycogen present in animal tissues. Another carnivorous fish, the sea bass (Lates calcarifer), also presented amylase activity in the digestive tract (SABAPATHY & TEO, 1992).

The highest total alkaline protease activity measured in the intestine was found at pH 8.0 and 8.5 for all fish species studied. However, some activity was also detected at pH 9.0 and 10.0 for all species, mainly in the anterior intestine. On the other hand, GARCIACARRENO et al. (2002) verified that the optimum pH for intestinal enzymes of Brycon orbignyanus was 10.0. The results observed at high alkaline pHs (9.0 and 10.0) are probably due to other alkaline proteases as carboxipeptidase-like, elastase-like or collagenase-like activities (HIDALGO et al., 1999).

The herbivore C. idella presented the highest amylase and maltase activities within the fish species studied, in accordance with CHAKRABARTI et al. (2006), who found high amylase activity in herbivorous fish. However, C. idella also presented alkaline protease, trypsin and chymotrypsin activities in the intestine. In agreement with the present study, KUZ'MINA & KUZ'MINA (1990) and CHAKRABARTI et al. (2006) also found high protease activity in non-carnivorous fish. In addition, the herbivorous Oreochromis niloticus (Nile tilapia) demonstrated higher carbohydrase activity than protease activity when compared to carnivorous and omnivorous fish (TENGJAROENKUL et al., 2000). Different authors have reported a close relationship between herbivorous feeding habits and higher amylase activity (HIDALGO et al., 1999; ODEDEYI & FAGBENRO, 2010).

In conclusion our study showed higher acid protease and trypsin activities in the carnivorous species studied, while higher amylase and maltase activities were found in the herbivorous species. Omnivorous species presented intermediate activity values. The results are within the expected range for each species and their feeding habits. The application of these feedings in the formulation of specific diets for each species using sources of low cost and good digestibility to fish.

http://dxs.doi.org/ 10.1590/0103-8478cr20160113

Received 02.04.16

Approved 05.30.16

Returned by the author 12.06.16 CR-2016-0113.R1

ACKNOWLEDGEMENTS

The authors thank Dr. Everton Behr for his technical help. V.L. Loro and B. Baldisserotto received research fellowships from Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq--Brazil).

REFERENCES

BALDISSEROTTO, B. et al. Jundia (Rhamdia sp.). In: BALDISSEROTTO, B.; GOMES, L.C. (Eds.). Especies nativas para piscicultura no Brasil. 2.ed. Santa Maria: UFSM, 2013. p.301-323.

BERNFELD, P. Amylases a and b: colorimetric assay methods. In: COLOWICK, S. P.; KAPLAN, N. O. Methods in Enzimology. New York: Academic, 1955. p.49-158.

BILLARD, R.; BERNI, P. Trends in cyprinid polyculture. Cybium, v.28, p.255-261, 2004. Avaliable from: <http://sfi.mnhn.fr/cybium/ numeros/2004/283/11-Billard193.pdf>. Accessed: Feb. 01, 2016.

BOYD, C. E.; TUCKER, C. S. Water quality and pond soil analyses for aquaculture. Alabama: Alabama Agricultural Experiment Station, Auburn University, 1992. 188p.

CHAKRABARTI, R. et al. Functional changes in digestive enzymes and characterization of proteases of silver carp (D and bighead carp ($) hybrid, during early ontogeny. Aquaculture, v.253, p.694-702, 2006. Avaliable from: <https://www.researchgate.net/profile/RajaRathore/ publication/232380390Functionalchangesindigestiveenzymesandchar acterizationofproteasesofsilvercarp%28%29andbigheadcarp%28%29 hybridduringearlyontogeny/links/0046351c18baa96e1400 0000.pdf>. Accessed: Feb. 01, 2016. doi: 10.1016/j.aquaculture.2005.08.018.

COLT, J. List of spreadsheets prepared as a complement. In: WEDEMEYER, G. A. (Ed). Fish hatchery management. 2. ed. Bethesda: American Fisheries Society Publications, 2002. 751p.

EATON, A. D. et al. Standard methods for the examination of water and wastewater. 21. ed. Washington: American Public Health Association, 2005. 1193p.

FILIPPOV, A. A. et al. Effects of organic pollutants on fish digestive enzymes: a review. Inland Water Biology, v.6, p.155-160, 2013. Available from: <http://link.springer.com/article/10.1134%2FS19950829130200 3X>. Accessed: Feb. 01, 2016. doi: 10.1134/S199508291302003X.

GARCIA-CARRENO, F. L. et al. Digestive proteinases of Brycon orbignyanus (Characidae, Teleostei): characteristics and effects of protein quality. Comparative Biochemistry and Physiology--Part B, v.132, p.343-352, 2002. Available from: <http://www.bashanfoundation. org/carreno/carrrenocharacidae.pdf>. Accessed: Feb. 01, 2016.

HIDALGO, M. C. et al. Comparative study of digestive enzymes in fish with different nutritional habits. Proteolytic and amylase activities. Aquaculture, v.170, p.267-283, 1999. Available from: <http://ac.els-cdn. com/S004484869800413X/1-s2.0-S004484869800413X-main.pdf?_ tid=cc3f0 85e-7c72-11e3-8614-00000aab0f26&acdnat=1389632004_81 ce406d86b8e1217d669d5a1545a 634> . Accessed: Jan. 13, 2014.

KUZ'MINA, V. V.; KUZ'MINA, Y. G. Level of total proteolytic activity in some species of fish from the Volga barin. Journal of Ichthyology, v.30, p.25-35, 1990.

LAZZARI, R. et al. Protein sources and digestive enzyme activities in jundia (Rhamdia quelen). Scientia Agricola, v.67, n.3, p.259-266, 2010. Avaliable from: <http://www.scielo.br/pdfZs/v67n 3/a02v67n3. pdf>. Accessed: Feb. 01, 2016.

LAZZARI, R et al. Utilizacao de residuos de frutas em dietas para piava. Boletim do Instituto de Pesca, v.41, n.2, p. 227-237, 2015. Avaliable from: <ftp://ftp.sp.gov.br/ftppesca/41_2_227-237.pdf>. Accessed: Feb. 01, 2016.

LOPEZ-VASQUEZ, K. et al. Digestive enzymes of eight Amazonian teleosts with different feeding habits. Journal of Fish Biology, v.74, p.1620-1628, 2009. Available from: <http://onlinelibrary.willey.com/ doi/10.1111/j.1095-8649.2009.02196.x/epdf>. Acessed: Feb. 01, 2016.

LOWRY, O. H. et al. Protein measurement with folin phenol reagent. Journal of Biological Chemistry, v.193, p.265-275, 1951.Avaliable from: <http://garfield.library.upenn.edu/classics1977/A1977DM02300001. pdf>. Accessed: Feb. 01, 2016.

LUNDSTEDT, L. M. et al. Digestive enzymes and metabolic profile of Pseudoplatystoma corruscans (Teleostei: Siluriformes) in response to diet composition. Comparative Biochemistry and Physiology --Part B, v.137, p.331-339, 2004. Available from: <http://ac.elscdn.com/S109649590303828/1-s2.0-S1096495903003828-main. pdf?tid=b8b1db7c-a4ec-11e6-91a2-00000aab0f01& acdnat=1478524 910_3f0b1e79f3d7dca29dfb1f70145f627a>. Accessed: Feb. 01, 2016.

MENIN, E.; MIMURA, O. M. Anatomia funcional da cavidade bucofaringeana de Hoplias malabaricus (Bloch, 1794) (Characiformes, Erythrinidae). Revista Ceres, v.38, p.240-255, 1991. Avaliable from: <http://www.ceres.ufv.br/ojs/index.php/ ceres/article/download/2137/188>. Accessed: Feb. 01, 2016.

ODEDEYI, D. O.; FAGBENRO, O. A. Feeding habits and digestive enzymes in the gut of Mormyrus rume (Valenciennes 1846) (Osteichthtes, Mormyridae). Tropical Zoology, v.23, p.75-89, 2010. Avaliable from: <https://www.researchgate.net/publication/287551841_Feeding_ habits_and_digestive_enzymes_in_the_gut_of_Mormyrus_rume_ Valenciennes_1846_Osteichth yes_Mormyridae>. Accessed: Feb. 01, 2016.

PARK, J. T; JOHNSON, M. J. A submicro determination of glucose. Journal of Biological Chemistry, v.181, p.149-151, 1949. Available from: <wwwjbc.org/content/181/1/149.long>. Accessed: Feb. 03, 2016.

PERETTI, D.; ANDRIAN, I. F. Feeding and morphological analysis of the digestive tract of four species of fish (Astyanax altiparanae, Parauchenipterus galeatus, Serrasalmus marginatus and Hoplias aff. malabaricus) from the upper Parana River floodplain, Brazil. Brazilian Journal of Biology, v.68, n.3, p.671-679, 2008. Avaliable from: <http:// www.scielo.br/scielo.php?pid= S1519-69842008000300027&script=sci_ arttext>. Accessed: Feb. 01, 2016. doi: 10.1590/S1519-698420080 00300027.

REYNALTE-TATAJE, D.; ZANIBONI-FILHO, E. Cultivo de piapara, piaucu, piava e piau--genero Leporinus. In: BALDISSEROTTO, B.; GOMES, L. C. (Eds). Especies nativas para piscicultura no Brasil. Santa Maria: UFSM, 2010. p.73-99.

SABAPATHY, U.; TEO, L. H. A quantitative study of some digestive enzymes in the rabbitfish, Siganus canaliculatus and the Sea bass, Lates calcarifer. Journal of Fish Biology, v.42, p.595-602, 1992. Avaliable from: <http://onlinelibrary.wiley.com/doi/10.1111/j.1095-8649.1993. tb003 62.x/pdf>. Accessed: Feb. 01, 2016. doi: 10.1016/S0022474X(00)00016-3.

TENGJAROENKUL, B. et al. Distribution of intestinal enzyme activities along the intestinal tract of cultured Nile tilapia, Oreochromis niloticus L. Aquaculture, v.182, p.317-327, 2000. Available from: <http://www.thaiscience.info/Article%20for%20ThaiScience/Article/2/ Ts-2%20distrib.of%20intestinal%20enzyme%20act.along%20 intestinal%20tract%20of%20cultured%20nile%20tilapia,%20 oreochromis%20niloticus%20l..pdf>. Accessed: Feb. 01, 2016.

Carolina Rosa Gioda (1) Alexandra Pretto (2) Carine de Souza Freitas (3) Jossiele Leitemperger (4) Vania Lucia Loro (4) Rafael Lazzari (5) Leandro Ademar Lissner (6) Bernardo Baldisserotto (3,7) Joseania Salbego (3) *

(1) Instituto de Ciencias Biologicas, Universidade Federal de Rio Grande (FURG), Rio Grande, RS, Brasil.

(2) Universidade Federal do Pampa (UNIPAMPA), Uruguaiana, RS, Brasil.

(3) Programa de Pos-graduacao em Farmacologia, Universidade Federal de Santa Maria (UFSM), Av. Roraima, 1000, 97105- 900, Santa Maria, RS, Brasil. E-mail: josalbego2004@yahoo.com.br. 'Corresponding author.

(4) Programa de Pos-graduacao em Bioquimica Toxicologica, Universidade Federal de Santa Maria (UFSM), Av. Roraima, 1000, Santa Maria, RS, Brasil.

(5) Departamento de Zootecnia e Ciencias Biologicas, Universidade Federal de Santa Maria (UFSM), Palmeira das Missoes, RS, Brasil.

(6) Universidade Federal do Pampa (UNIPAMPA), Cacapava do Sul, RS, Brasil.

(7) Departamento de Fisiologia e Farmacologia, Programa de Pos-graduacao em Farmacologia e Zootecnia, Universidade Federal de Santa Maria (UFSM), Santa Maria, RS, Brasil.

Caption: Figure 1--Amylase activity at different pHs in the anterior (A) and [min.sup.-1] (B) intestine and stomach (C) of the studied species. Activity is expressed as U mg [protein.sup.-1], where U=1 [micro]mol glucose min mg [protein.sup.-1]. Data represent mean [+ or -] SEM (n=10). * Represents the pH at which the enzyme has the highest activity.

Caption: Figure 2--Alkaline protease activity at different pHs in the anterior (A) and mid (B) intestine and acid protease activity in the stomach (C) of the studied species. Activity is expressed as U mg [protein.sup.-1], where U=1 [micro]g tyrosine [min.sup.-1] mg [protein.sup.-1]. Data represent mean [+ or -] SEM (n=10). * Represents the pH at which the enzyme has the highest activity.

Caption: Figure 3--Amylase (A) and maltase (B) activities in anterior, middle and posterior intestine of the studied species. Activity is expressed as U mg protein-1, where U=1 [micro]mol glucose [min.sup.-1] mg [protein.sup.-1]. Trypsin (C) and chymotrypsin (D) activity in anterior, middle and posterior intestine of the studied species. Activity is expressed as U mg protein-1, where U = g of substrate hydrolyzed (TAME or BTEE) [min.sup.-1] mg [protein.sup.-1]. Data represent mean [+ or -] SEM (n=10). 'Represents the portion of the intestine where the highest activity is observed for each enzyme.
Table 1--Trypsin, chymotrypsin and maltase activities in the stomach
of the studied species data on enzyme digestive activities (n=10) are
expressed as U mg protein-1 where U=1pmol of substrate hydrolyzed
min-1. Different superscript letters represent significant difference
of digestive enzymes activity comparing different fish species
(P<0.05).

Species                        Trypsin

Rhamdia quelen         0.102 [+ or -] 0.027 (c)
Leporinus obtusidens   0.362 [+ or -] 0.031 (b)
Hoplias malabaricus    1.150 [+ or -] 0.11 (a)

Species                     Chymotrypsin

Rhamdia quelen         114.6 [+ or -] 11.7 (a)
Leporinus obtusidens   71.86 [+ or -] 16.5 (b)
Hoplias malabaricus    113.5 [+ or -] 12.6 (a)

Species                       Maltase

Rhamdia quelen         1.30 [+ or -] 0.36 (a)
Leporinus obtusidens   1.62 [+ or -] 0.29 (b)
Hoplias malabaricus    1.14 [+ or -] 0.19 (a)
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Title Annotation:texto en ingles
Author:Gioda, Carolina Rosa; Pretto, Alexandra; Freitas, Carine de Souza; Leitemperger, Jossiele; Loro, Van
Publication:Ciencia Rural
Date:Mar 1, 2017
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