Time-dependent modulation of post-hatch cortisol and antioxidant responses in Melanotaenia boesemani embryos exposed to potassium derived from banana peel ash extract

Responses of M. boesemani to potassium exposure

Authors

  • Intanurfemi B Hismayasari Department of Aquaculture, Faculty of Marine and Fisheries, Brawijaya University, Jl. Veteran Ketawanggede Lowokwaru Malang, 65145, Indonesia; Sorong Polytechnic of Marine and Fisheries, Jl. Kapitan Pattimura Maladumes, Sorong, 98411, Papua Barat Daya, Indonesia https://orcid.org/0000-0001-5731-1473
  • Mohamad Fadjar Department of Aquaculture, Faculty of Marine and Fisheries, Brawijaya University, Jl. Veteran Ketawanggede Lowokwaru Malang, 65145, Indonesia
  • Abdul Rahem Faqih Department of Aquaculture, Faculty of Marine and Fisheries, Brawijaya University, Jl. Veteran Ketawanggede Lowokwaru Malang, 65145, Indonesia
  • Wahyu Endra Kusuma Department of Aquaculture, Faculty of Marine and Fisheries, Brawijaya University, Jl. Veteran Ketawanggede Lowokwaru Malang, 65145, Indonesia
  • Ernawati Ernawati Bone Polytechnic of Marine and Fisheries, Jl. Sungai Musi KM. 9, Kelurahan Waetuo / Pallette, Kecamatan Tanete Riattang Timur, Kabupaten Bone, 92718, Sulawesi Selatan, Indonesia https://orcid.org/0009-0000-2849-8240

DOI:

https://doi.org/10.62310/liab.v6i2.425

Keywords:

Stress response, Potassium exposure, Melanotaenia boesemani, Cortisol, Antioxidant enzymes, Survival

Abstract

Embryonic exposure to ionic disturbance can alter post hatch stress regulation in fish. This study examined whether immersion duration in potassium-rich banana peel ash extract affected endocrine and antioxidant responses in Melanotaenia boesemani. Embryos were immersed in a fixed potassium concentration of BPA extract (13.5 mg L-1) for 15.5, 24, and 32.5 h, alongside untreated and KCl reference groups (three biological replicates per treatment). Cortisol, superoxide dismutase (SOD), and catalase (CAT) were quantified at 7 days post hatching, and survival was recorded at 60 days post-hatching. Data were analyzed using one-way ANOVA with Tukey HSD, Pearson correlation, and principal component analysis (PCA). All four endpoints (cortisol, SOD, CAT, and survival rate) differed significantly among treatments (p<0.05). Cortisol was significantly higher in all BPA-exposed groups than in both controls, reaching its highest numerical value at 24 h, although the three BPA-duration groups did not differ significantly from one another. SOD and CAT activities increased with BPA exposure, reaching their highest values at 24 h. CAT remained significantly elevated relative to the controls and the 15.5 h group at both 24 and 32.5 h, whereas SOD was significantly elevated relative to the controls and the 15.5 h group only at 24 h. SR declined progressively with increasing immersion duration and was lowest at 32.5 h. Cortisol correlated positively with SOD (r = 0.86) and CAT (r = 0.81), and SOD correlated strongly with CAT (r = 0.87). Survival rate was negatively correlated with cortisol (r = -0.59) and CAT (r = -0.75). PCA reduced the four variables into two components explaining 94.3% of total variance and separated BPA exposed groups from controls along a biomarker dominated axis. These results indicate a coordinated endocrine and antioxidant response following embryonic BPA exposure, but the magnitude of the biomarkers was not directly related to survival outcome. The highest biomarker responses at 24 h coincided with intermediate survival, while the lowest survival at 32.5 h occurred alongside declining biomarker levels. This dissociation indicates that immersion duration itself, independent of potassium concentration, is an important variable to consider when evaluating biomass-derived potassium sources for use during early developmental stages.

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References

Akhsan WM, Nur B, Dewi NN. (2020). Growth performance and survival rate of Boeseman’s rainbowfish (Melanotaenia boesemani) in natural spawning technique at Depok, West Java, Indonesia. IOP Conference Series: Earth and Environmental Science 441(1): 012037. https://doi.org/10.1088/1755-1315/441/1/012037

Alasmari AF, Ali N, Alasmari F, Alanazi WA, Alqahtani F, Alharbi M, Alotaibi FM, Aldossari AA, Alswayyed M, Alanazi MM, Alshamrani AA. (2020). Elucidation of the molecular mechanisms underlying sorafenib-induced hepatotoxicity. Oxidative Medicine and Cellular Longevity 2020(1): 7453406. https://doi.org/10.1155/2020/7453406

Aldurrah Z, Mohd Kauli FS, Abdul Rahim N, Zainal Z, Afzan A, Al Zarzour RH, Muhamad Salhimi S, Che Zain MS, Zakaria F. (2023). Antidepressant evaluation of Andrographis paniculata Nees extract and andrographolide in chronic unpredictable stress zebrafish model. Comparative Biochemistry and Physiology Part C: Toxicology and Pharmacology 271: 109678. https://doi.org/10.1016/j.cbpc.2023.109678

Bai Z, Bao Z, Hu H. (2025). Chemical recycling of catalytic glycolysis of polyethylene terephthalate with potassium-rich biomass. Recycling 10(3): 85. https://doi.org/10.3390/recycling10030085

Castillo-Ramírez LA, Ryu S, De Marco RJ. (2024). Cortisol dynamics and GR-dependent feedback regulation in zebrafish larvae exposed to repeated stress. Biology Open 13(10): 1–7. https://doi.org/10.1242/bio.061683

Culbert BM, Regish AM, Hall DJ, McCormick SD, Bernier NJ. (2022). Neuroendocrine regulation of plasma cortisol levels during smoltification and seawater acclimation of Atlantic salmon. Frontiers in Endocrinology 13: 859817. https://doi.org/10.3389/fendo.2022.859817

Dagoudo M, Mutebi ET, Qiang J, Tao YF, Zhu HJ, Ngoepe TK, Xu P. (2023). Effects of acute heat stress on haemato-biochemical parameters, oxidative resistance ability, and immune responses of hybrid yellow catfish (Pelteobagrus fulvidraco × P. vachelli) juveniles. Veterinary Research Communications 47(3): 1217–1229. https://doi.org/10.1007/s11259-022-10062-1

de Fátima Pereira de Faria C, de Andrade BU, Urbinati EC. (2025). Physiological responses of pacu (Piaractus mesopotamicus) to intermittent cold exposure: A comprehensive analysis of stress, immunity, antioxidant, and metabolic adaptations. Fish Physiology and Biochemistry 51(1): 1–21. https://doi.org/10.1007/s10695-024-01445-z

Gupta S, Roy S. (2024). Captive culture of Boeseman’s rainbowfish (Melanotaenia boesemani): First approach in Indian perspective. Research Journal of Agricultural Sciences 15(2): 327–330.

Han S, Han L, Yuan F, Liu W, Wang J, Jin X, Sun Y. (2025). Exploring disparities in gill physiological responses to NaHCO3-induced habitat stress in triploid and diploid crucian carp (Carassius auratus): A comprehensive investigation through multi-omics and biochemical analyses. Metabolites 15(1): 5. https://doi.org/10.3390/metabo15010005

Hismayasari IB, Fadjar M, Faqih AR, Kusuma WE, Kusrini E, Syahidah D, Pattirane CP, Herlina C. (2026). Comparison of the toxicity of bio-based and synthetic potassium in Melanotaenia boesemani embryos. Letters in Animal Biology 6(1): 108–117. https://doi.org/10.62310/liab.v6i1.401

Li X, Dai Y, Li X, Guo H, Dai J, Wang H, Xiong D, Liao G. (2025). Oxidative stress responses and recovery of marine medaka (Oryzias melastigma) in early-life stages after acute exposure to crude oil. Journal of Marine Science and Engineering 13(5): 965. https://doi.org/10.3390/jmse13050965

Liu Z, Shangguan Y, Zhu P, Sultan Y, Feng Y, Li X, Ma J. (2022). Developmental toxicity of glyphosate on embryo-larval zebrafish (Danio rerio). Ecotoxicology and Environmental Safety 236: 113493. https://doi.org/10.1016/j.ecoenv.2022.113493

Mezzomo NJ, Fontana BD, Müller TE, Duarte T, Quadros VA, Canzian J, Pompermaier A,

Soares SM, Koakoski G, Loro VL, Rosemberg DB, Barcellos LJG. (2019). Taurine modulates the stress response in zebrafish. Hormones and Behavior 109: 44–52. https://doi.org/10.1016/j.yhbeh.2019.02.006

Nathaniel P, Varghese T, S TC, Deo AD, K N, K V, Bhatt S, B S, Akhila S, Gupta S. (2026). Heatwave duration modulates physio-biochemical responses in genetically improved farmed tilapia (Oreochromis niloticus) under simulated conditions. Fish Physiology and Biochemistry 52(4): 109. https://doi.org/10.1007/s10695-026-01728-7

Opinion AGR, Vanhomwegen M, De Boeck G, Aerts J. (2023). Long-term stress-induced cortisol downregulation, growth reduction and cardiac remodeling in Atlantic salmon. Journal of Experimental Biology 226(22): 246504. https://doi.org/10.1242/jeb.246504

Putra NR, Aziz AHA, Faizal ANM, Che Yunus MA. (2022). Methods and potential in valorization of banana peels waste by various extraction processes: In review. Sustainability 14(17): 10571. https://doi.org/10.3390/su141710571

Raposo de Magalhães C, Farinha AP, Blackburn G, Whitfield PD, Carrilho R, Schrama D, Cerqueira M, Rodrigues PM. (2022). Gilthead seabream liver integrative proteomics and metabolomics analysis reveals regulation by different prosurvival pathways in the metabolic adaptation to stress. International Journal of Molecular Sciences 23(23): 15395. https://doi.org/10.3390/ijms232315395

Shaughnessy CA, Myhre VD, Hall DJ, McCormick SD, Dores RM. (2023). Hypothalamus-pituitary-interrenal (HPI) axis signaling in Atlantic sturgeon (Acipenser oxyrinchus) and sterlet (Acipenser ruthenus). General and Comparative Endocrinology 339: 114290. https://doi.org/10.1016/j.ygcen.2023.114290

Ullah R, Ghayyur S, Samad SU, Arshad SM, Ghayyur S, Shah R, Arif S. (2026). Integrated biomarker responses and multivariate assessment of polyethylene microplastics toxicity in the endemic freshwater fish Tor putitora. Environmental Geochemistry and Health 48(2): 1–28. https://doi.org/10.1007/s10653-025-02963-2

Valcarce DG, Sellés-Egea A, Riesco MF, De Garnica MG, Martínez-Fernández B, Herráez MP, Robles V. (2024). Early stress exposure on zebrafish development: Effects on survival, malformations and molecular alterations. Fish Physiology and Biochemistry 50(4): 1545–1562. https://doi.org/10.1007/s10695-024-01355-0

Vieira RSF, Venâncio CAS, Félix LM. (2025). Behavioral, metabolic, and biochemical alterations caused by an acute stress event in a zebrafish larvae model. Fish Physiology and Biochemistry 51(1): 1–14. https://doi.org/10.1007/s10695-024-01421-7

Wang X, Ma A, Huang Z, Sun Z, Liu Z. (2022). Genetic mechanism for antioxidant activity of endogenous enzymes under salinity and temperature stress in turbot (Scophthalmus maximus). Antioxidants 11(10): 2062. https://doi.org/10.3390/antiox11102062

Xu H, Miao XM, Wang WB, Wang G, Li Y. (2022). Transcriptome analysis reveals the early resistance of zebrafish larvae to oxidative stress. Fish Physiology and Biochemistry 48(4): 1075–1089. https://doi.org/10.1007/s10695-022-01100-5

Yuan M, Fang Q, Lu W, Wang X, Hao T, Chong CM, Chen S. (2025). Stress in fish: Neuroendocrine and neurotransmitter responses. Fishes 10(7): 307. https://doi.org/10.3390/fishes10070307

Zare M, Heidari E, Hosseini Choupani SM, Akhavan SR, Rombenso A, Esmaeili N. (2023). The recovery time between early mild stress and final acute stress affects survival rate, immunity, health, and physiology of Oscar (Astronotus ocellatus). Animals 13(10): 1606. https://doi.org/10.3390/ani13101606

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Published

12-09-2026

How to Cite

Hismayasari, I. B., Fadjar, M., Faqih, A. R. ., Kusuma, W. E., & Ernawati, E. (2026). Time-dependent modulation of post-hatch cortisol and antioxidant responses in Melanotaenia boesemani embryos exposed to potassium derived from banana peel ash extract: Responses of M. boesemani to potassium exposure. Letters in Animal Biology, 6(2), 89–96. https://doi.org/10.62310/liab.v6i2.425

Issue

Section

Research Articles
Recieved 2026-08-11
Accepted 2026-09-04
Published 2026-09-12

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