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Histomorphogenesis on hindbrain in Huso huso (Beluga sturgeon) larvae

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Abstract

This study has been done on evolution and morphology of hindbrain structure, during larvae life from 1 to 54 dph on Huso huso. It was concentrated on significant cerebellum and medulla oblongata. The cerebellum occupied the rostral part of dorsal wall of fourth ventricle. The fourth ventricle was visible on 1 day old and by aging was majorly. The fourth ventricle lied on the caudally and continued into central canal (cc) in spinal cord. Cortex of cerebellum had three layers, which were visible from 6 days old. Granular layer of corpus cerebelli, eminentia granularis, and less valvula cerebelli contained Golgi type II, and purkinje cells and observed from 6 days old clearly. Three sulci recognized in cerebellum on 15 days old. Medulla oblongata located at the caudal part of cerebellum and observed from 1 day old and contained eminentia granulares and crista cerebellares. Nucleuses of facial and vagal nerves were in ventral thick part of medulla oblongata. This structure, similar to cerebellum had columns of columnar cells in its gray matter. The white and gray matter, in hindbrain was visible on 1 and 3 days old, and from 6 days old the rate of white matter increased. Stereological results showed that there were significantly distinctive regional differences in the volume of different parts of hindbrain represented a correlation and was P < 0.05. Generally, in H. huso larvae from 1 to 54 days old, the volume of hindbrain had a significant increased such that it had the largest volume in fish brain compare to other parts.

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References

  • Bauchot R, Bauchot ML, Platel R, Ridet JM (1977) Brains of Hawaiian tropical fishes; brain size and evolution. Copeia 1977:42–46

    Article  Google Scholar 

  • Brandstatter R, Kotrschal K (1989) Life history of roach, Rutilus rutilus (cyprinidae, Teleostei). Brain Behav Evol 34:35–42

    Article  CAS  PubMed  Google Scholar 

  • Broglio C, Rodriquez R, Salas C (2003) Spatial cognition and its neural basis in teleost fishes. Fish Fisher 4:274–255

    Article  Google Scholar 

  • Burr HS (1928) The central nervous system of Orthagoriscus mola. J Comp Neurol 45:33–128

    Article  Google Scholar 

  • Butler AB, Hodos W (2005) Comparative vertebrate neuroanatomy, evolution and adaptation, 2th edition, United States of America

  • Davis RE, Northcutt RG (eds) (1983) Fish neurobiology, vol II. The university of Michigan Press, Ann Arbor

    Google Scholar 

  • Eaton RC, Lee RK, Foreman MB (2001) The Mauthner cell and other identified neurons of the brainstem escape network of fish. Prog Neurobiol 63:467–485

    Article  CAS  PubMed  Google Scholar 

  • Evans HM (1935) The brain of Gadus, with special reference to the medulla oblongata and its variations according to the feeding habits if different Gadidae – I. Proc R Soc Lond B Biol Sci 117B:367–399

    Google Scholar 

  • Evans H M (1940) Brain and body fish. A Study of Brain Pattern in Relation to Hunting and Feeding in Fish London: The Technical Press Ltd pp 164

  • Finger TE (1988) Organization of chemosensory systems within the brains of bony fish. In: Atema J, Fay RR, Popper AN, Tavolga WN (eds) Sensory biology of aquatic animals. Speringer-Verlag, New York, NY, pp 339–364

    Chapter  Google Scholar 

  • Gibbs MA, Northcutt RG (2004) Development of the lateral line system in the shovelnose sturgeon. Brain Behav Evol 64:70–84

    Article  PubMed  Google Scholar 

  • Gundersen HJG, Jensen EB (1987) The efficiency of systematic sampling in stereology and its prediction. J Microsc 147:263–229

    Article  Google Scholar 

  • Helfman G, Collette B, Facey D (1997) The diversity of fishes, vol 544. Blackwell publishing, London

    Google Scholar 

  • Hernando J A, Domezain A, Zabala C, Domezain J, Cabrera R, Soriguer M C (2005) Desarrollo de las aletas pectorales durante la morfogenesis de Acipenser naccarii, Bonaparte 1836. In: IX Congreso Nacional de Acuiculture. Abstract Book. Junta de Andalucia, Cadiz, pp 81–85

  • Huesa G, Anadon R, Yanez J (2003) Afferent and efferent connections of the cerebellum of the chondrostean Acipenser baerii. A carbocyanine dye (DiL) tracing study. J Comp Neurol 460:327–344

    Article  PubMed  Google Scholar 

  • Ito H, Ishikawa Y, Yoshimoto M, Yoshimoto N (2007) Diversity of brain morphology in teleost: brain and ecological niche. Brain Behav Evol 69:76–86

    Article  PubMed  Google Scholar 

  • Johnston JB (1898) Hindbrain and cranial nerves of Acipenser. Anat Anz 14:580–602

    Google Scholar 

  • Kimley AP, Beavers SC, Curtis TH, Jorgensen SJ (2002) Movements and swimming behavior of three species of sharks in La Jolla Canyon, California. Environ Biol Fishes 63:117–135

    Article  Google Scholar 

  • Kotrschal K, Van Staaden MJ, Huber R (1998) Fish brains: evolution and environmental relationships. Rev Fish Biol Fish 8:373–408

    Article  Google Scholar 

  • Lauder GV, Liem K (1983) The evolution and inter relationships of the actinopterygian fishes. Bull Mus Comp Zool 150:95–197

    Google Scholar 

  • McCormik CA (1982) The organization of the octavolateralis area in actinopterygian fishes: a new interpretation. J Morphol 171:159–181

    Article  Google Scholar 

  • Meek J, Nieuwenhuys R (1998) Holosteans and teleosts. In: Nieuwenhuys R, Ten Donkelaar HJ, Nicholson C (eds) The central nervous system of vertebrates. Springer, Berlin, pp 760–937

    Google Scholar 

  • Nieuwnhuys R (1967) Comparative anatomy of cerebellum. Prog Brain Res 15:1–93

    Google Scholar 

  • Nieuwnhuys R (1998) Chondrostean fishes. In: Nieuwnhuys R, Ten Donkelaar HJ, Nicholson C (eds) The central nervous system of vertebrates. Speringer Verlag, Berlin, pp 701–757

    Chapter  Google Scholar 

  • Norris HW (1925) Observations upon the peripheral distribution of the cranial nerves of certain ganoids fishes (Amia, Lepidosteus, Polyodon, Scaphyrrinchus, and Acipenser). J Comp Neurol 39:345–432

    Article  Google Scholar 

  • Northcutt RG (1978) Brain organization in the cartilaginous fishes. In: Hodgson ES, Mathewson RF (eds) Sensory biology of sharks, skates and rays. Office of Naval Research, Arlington, pp 117–193

    Google Scholar 

  • Northcutt RG (1996) The agnathan ark: the origin of craniate brains. Brain Behav Evol 48:237–247

    Article  CAS  PubMed  Google Scholar 

  • Northcutt RG, Davis RE (1983) Fish neurobiology. University of Michigan Press, Ann Arbor

    Google Scholar 

  • Popper AN, Fay RR (1993) Sound detection and processing by fish: critical review and major research questions. Brain Behav Evol 41:14–38

    Article  CAS  Google Scholar 

  • Pouwels E (1978) On the development of the cerebellum of the trout, Salmo gairdneri. I. Patterns of cell migration. Anat Embryol 152:291–308

    Article  CAS  PubMed  Google Scholar 

  • Singh CP (1972) A comparative observation of the brain of some Indian freshwater teleost, with special reference to their feeding habits. Anat Anz 131:377–422

    Google Scholar 

  • Teeter JH, Szamier RB, Bennet MVL (1980) Ampullary electroreceptors in the sturgeon Scaphirhynchus platorynchus (Rafinesque). J Comp Physiol 138:213–233

    Article  Google Scholar 

  • Theunissen F (1914) The arrangements of the motor roots and nuclei in the brain of Acipenser ruthenus and Lepisosteus osseus. Proc Kon Ned Akad Wet (Amsterdam) 16:1032–1041

    Google Scholar 

  • Vazquez M, Rodriguez F, Domezain A, Salas C (2002) Development of the brain of the sturgeon Acipenser naccarii. Piscifactoria de Sierra Nevada, Riofrio, Granada, Spain. Appl Ichthyol 18:275–279

    Article  Google Scholar 

  • Wagner HJ (2003) Volumetric analysis of brain areas indicates a shift in sensory orientation during development in the deep-sea grenadier Coryphaenoides armatus. Mar Biol 142:791–797

    Article  Google Scholar 

Download references

Acknowledgments

Thanks to Dr. Tavighi for practical assistance and labor on the thesis, Dr. Shojaei for embryology information, and Dr. Behnam Rassouli for stereological technique.

Funding

The study was supported by the Faculty of Veterinary Science Ferdowsi University of Mashhad, Iran, (Grant number455).

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All authors contributed equally to this work and are responsible for the data presented herein.

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Correspondence to Sherma Tavighi.

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The authors declare that they have no conflict of Interest.

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The study protocol was approved by the Animal Care and Use Committee, Faculty of Veterinary Science, Ferdowsi University, Iran (Animal Use Protocol No.140).

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This article does not contain any studies with human participants performed by any of the authors.

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Tavighi, S., Saadatfar, Z., Shojaei, B. et al. Histomorphogenesis on hindbrain in Huso huso (Beluga sturgeon) larvae. Comp Clin Pathol 28, 783–791 (2019). https://doi.org/10.1007/s00580-019-02915-0

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