Effects of salinity on gills' chloride cells, stress indices, and gene expression of Asian seabass (Lates calcarifer, Bloch, 1790).

Asian seabass Cortisol Heat shock proteins Immune-related genes Ionocytes

Journal

Fish physiology and biochemistry
ISSN: 1573-5168
Titre abrégé: Fish Physiol Biochem
Pays: Netherlands
ID NLM: 100955049

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 21 05 2021
accepted: 07 10 2021
pubmed: 31 10 2021
medline: 24 2 2022
entrez: 30 10 2021
Statut: ppublish

Résumé

A 2-week research was carried out to assess water salinity (WS) effects including 0, 15, 35, and 50‰ on osmoregulatory mechanisms and stress indices in Asian sea bass (34.4 g) juveniles. Except for fish reared at 50‰, in the other treatments, it gradually decreased to the prescribed WS during a 10-day period (- 5‰ a day). After a 10-day acclimation period, fish were reared at the prescribed WS for 2 weeks. Fish reared at 15 and 35‰ had higher chloride cell (CC) counts in the interlamellar region. The number of CC in the interlamellar region elevated with increment of WS up to 35‰, but they were pronouncedly reduced in 50‰ group. The diameter of CC in the interlamellar region was not affected by WS. The smallest nucleus diameter of CC in the interlamellar region was observed in fish reared at 15‰ (P < 0.05). The largest and the smallest amounts of serum aspartate aminotransferase were observed in fish reared at freshwater and 15‰, respectively. Fish reared at 35‰ had the highest serum sodium and potassium contents. Serum chloride content and total osmolality increased with increment of WS (P < 0.05). Serum cortisol and glucose contents gradually increased with elevation of WS up to 35‰; then, their contents remarkably decreased. The relative expression of insulin like growth factor-1 in the liver of fish reared at 35‰ was strikingly higher than that in the other groups. The relative expression of HSP70 gene in fresh water group was pronouncedly elevated compared to other treatments. The relative expression of interleukin-1β in 15 and 35‰ groups was higher than that in the other groups; however, the relative expression of lysozyme gene in the liver of fish reared at fresh water was pronouncedly lower than that in the other treatments. The results of this study suggested rearing L. calcarifer at 15‰ closer to the isosmotic point and better provide its welfare.

Identifiants

pubmed: 34716532
doi: 10.1007/s10695-021-01024-6
pii: 10.1007/s10695-021-01024-6
doi:

Substances chimiques

Chlorides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2027-2039

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Nature B.V.

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Auteurs

Maryam Azodi (M)

Persian Gulf Research Institute, University of Persian Gulf, 7516913798, Bushehr, Iran.

Mahmoud Nafisi Bahabadi (MN)

Persian Gulf Research Institute, University of Persian Gulf, 7516913798, Bushehr, Iran.
Department of Fisheries and Biology, Persian Gulf Research Institute, Persian Gulf University, 7516913798, Bushehr, Iran.

Ahmad Ghasemi (A)

Persian Gulf Research Institute, University of Persian Gulf, 7516913798, Bushehr, Iran.

Vahid Morshedi (V)

Persian Gulf Research Institute, University of Persian Gulf, 7516913798, Bushehr, Iran. v.morshedi@gmail.com.

Mansour Torfi Mozanzadeh (MT)

Agricultural Research Education and Extension Organization (AREEO), South Iran Aquaculture Research Centre, Iranian Fisheries Science Institute (IFSRI), Ahwaz, Iran. mansour.torfi@gmail.com.

Raheleh Shahraki (R)

Department of Basic Sciences, Division of Histology, Faculty of Veterinary Medicine, Shahid Chamran University, Ahwaz, Iran.

Omid Khademzadeh (O)

Department of Fisheries, Faculty of Marine Natural Resources, Khorramshahr University of Marine Science and Technology, Khorramshahr, Iran.

Shirin Hamedi (S)

Persian Gulf Research Institute, University of Persian Gulf, 7516913798, Bushehr, Iran.

Sakineh Avizhgan (S)

Persian Gulf Research Institute, University of Persian Gulf, 7516913798, Bushehr, Iran.

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