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Organogenesis of exocrine pancreas in sharpsnout sea bream (Diplodus puntazzo) larvae: characterization of trypsin expression

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Abstract

The ontogeny and differentiation stages of digestive systems related with trypsin expression in larvae of sharpsnout sea bream, Diplodus puntazzo, were investigated from hatching to 40 DAH (days after hatching), and total lengths and weights of larvae were determined. Histologic and enzymatic techniques were used to explain the functional development of the pancreas including trypsin activity. The pancreas was identified as a compact structure located in the region slightly posterior to the liver. At 3 DAH, first anus and then mouth opened. Incipient pancreas secretion polyhedral cells could be first observed as zymogen granules. During larval metamorphosis, the pancreas became diffuse, spreading throughout the mesentery in proximity to the stomach, the anterior intestine and the pyloric caeca. The specific activity of trypsin (42.54 ± 6.8 mU/mg protein−1) was found as early as after hatching at larvae size of 2.87 ± 0.34 mm at 0 DAH. Activity further increased until 10 DAH, especially after exogenous feeding. The highest trypsin activity was detected at 25 DAH as 119.26 ± 11.6 mU/mg protein−1. It is concluded that exocrine pancreas organogenesis is the main critical step in the development of digestive system that results in zymogen granules accumulation and increased trypsin activity.

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References

  • Aktülün S, Suzer C, Kamacı HO, Çoban D, Saka Ş, Fırat K (2008) Activity of the digestive protease, chymotrypsin, in larvae of the cultured sharpsnout seabream (Diplodus puntazzo) larvae. The Israeli J Aquac Bamidgeh 60(2):82–88

    Google Scholar 

  • Boglione C, Giganti M, Selmo C, Cataudella S (2003) Morphoecology in larval fin fish: a new candidate species for aquaculture, Diplodus puntazzo (Sparidae). Aquacult Int 11:17–41

    Article  CAS  Google Scholar 

  • Bradford MM (1976) A rapid sensitive method for the quantification of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254

    Article  CAS  PubMed  Google Scholar 

  • Cahu CL, Zambonino Infante JL (2001) Substitution of live food by formulated diets in marine fish larvae. Aquaculture 200:161–180

    Article  Google Scholar 

  • Caruso G, Genovese L, Micale V, Spedicato MT, Mancuso M (2001) Preliminary investigation of the digestive enzymes in Pagellus erythrinus (Linneo 1758) larvae. Mar Freshw Behav Physiol 34:265–268

    Article  CAS  Google Scholar 

  • Chen BN, Qin JG, Kumar SM, Hutchinson WG, Clarke SM (2006) Ontogenetic development of digestive enzymes in yellowtail kingfish Seriola lalandi larvae. Aquaculture 260:264–271

    Article  CAS  Google Scholar 

  • Guyot E, Dı’az JP, Connes R (1995) Organogenesis of the liver in sea bream Sparus aurata. J Fish Biol 47:427–437

    Article  Google Scholar 

  • Kolkovski S (2001) Digestive enzymes in fish larvae and juveniles-implications and application to formulated diets. Aquaculture 200:181–201

    Article  CAS  Google Scholar 

  • Micale V, Garaffo M, Genovese L, Spedicato MT, Muglia U (2006) The ontogeny of the alimentary tract during larval development in common pandora Pagellus erythrinus, L. Aquaculture 251:354–365

    Article  Google Scholar 

  • Micale V, Di Giancamillo A, Domeneghini C, Mylonas CC, Nomikos N, Papadakis IE, Muglia U (2008) Ontogeny of the digestive tract in sharpsnout sea bream Diplodus puntazzo (Cetti, 1777). Histol Histopathol 23:1077–1091

    CAS  PubMed  Google Scholar 

  • Moyano FJ, Diaz M, Alarcon FJ, Sarasquete MC (1996) Characterisation of digestive enzyme activity during larval development of gilthead seabream (Sparus aurata). Fish Physiol Biochem 15:121–130

    Article  CAS  Google Scholar 

  • Nolting M, Ueberschär B, Rosenthal H (1999) Trypsin activity and physiological aspects in larval rearing of European sea bass (Dicentrarchus labrax) using live prey and compound diets. J Appl Ichthyol 15:138–142

    Article  CAS  Google Scholar 

  • Papandroulakis N, Kentouri M, Maingot E, Divanach P (2004) Mesocosm: a reliable technology for larval rearing of Diplodus puntazzo and Diplodus sargus sargus. Aquacult Int 12:345–355

    Article  Google Scholar 

  • Ribeiro L, Sarasquete C, Dinis MT (1999) Histological and histochemical development of the digestive system of Solea senegalensis (Kaup, 1858) larvae. Aquaculture 171:293–308

    Article  CAS  Google Scholar 

  • Santamaria CA, Marin de Mateo M, Traveset R, Sala R, Grau A, Pastor E, Sarasquete C, Crespo S (2004) Larval organogenesis in common dentex Dentex dentex L. (Sparidae): histological and histochemical aspects. Aquaculture 237:207–228

    Article  Google Scholar 

  • Sarasquete C, Polo A, Yu’fera M (1995) Histology and histochemistry of the development of the digestive system of larval gilthead seabream Sparus aurata L. Aquaculture 130:79–92

    Article  Google Scholar 

  • Suzer C, Fırat K, Saka Ş (2006) Ontogenic development of the digestive enzymes in common pandora, Pagellus erythrinus, L. larvae. Aquac Res 37:1565–1571

    Article  Google Scholar 

  • Suzer C, Aktülün S, Çoban D, Kamacı HO, Saka Ş, Fırat K, Alpbaz A (2007a) Digestive enzyme activities in sharpsnout seabream (Diplodus puntazzo) larvae. Comp Biochem Physiol 148A(2):470–477. doi:10.1016/j.cbpa.2007.06.418

    CAS  Google Scholar 

  • Suzer C, Kamacı HO, Çoban D, Saka Ş, Fırat K, Ozkara B, Ozkara A (2007b) Digestive enzyme activity of the red porgy (Pagrus pagrus, L.) during larval development under culture conditions. Aquacult Res 38(16):1778–1785. doi:10.1111/j.1365-2109.2007.01841.x

    Article  CAS  Google Scholar 

  • Tseng HC, Grendell JH, Rothman SS (1982) Food, deodenal extracts, and enzyme secretion by the pancreas. Am J Physiol 243:G304–G312

    CAS  PubMed  Google Scholar 

  • Zambonino Infante JL, Cahu CL (2001) Ontogeny of the gastrointestinal tract of marine fish larvae. Comp Biochem Physiol 130C(3):477–487. doi:10.1016/S1532-0456(01)00274-5

    CAS  Google Scholar 

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Acknowledgments

The authors would like to express our sincere gratitude to Assoc. Prof. Dr. Hakan POSTACI for the excellent cooperation for histological analysis and also the staff of the Teknomar Sea Fish Broodstock Centre where the experiments were conducted (Akuvatur Mediterranean Sea Foods, Izmir, TURKEY) for their most efficient technical assistance.

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Correspondence to H. Okan Kamaci.

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Kamaci, H.O., Suzer, C., Çoban, D. et al. Organogenesis of exocrine pancreas in sharpsnout sea bream (Diplodus puntazzo) larvae: characterization of trypsin expression. Fish Physiol Biochem 36, 993–1000 (2010). https://doi.org/10.1007/s10695-009-9377-8

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  • DOI: https://doi.org/10.1007/s10695-009-9377-8

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