All-male production in Nile tilapia (Oreochromis niloticus) through discrete anastrozole immersion: hormonal and histological insights.

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Hauptverfasser: Katare, Milind B, Mogalekar, Havagiappa S, Swami, Aarti M, Singh, Mukesh K, Lende, Smit R, Chanu, Sanjarambam Nirupama, Marak, Senrita Raksam
Format: Artículo científico
Sprache:en
Veröffentlicht: Fish physiology and biochemistry 2026
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author Katare, Milind B
Mogalekar, Havagiappa S
Swami, Aarti M
Singh, Mukesh K
Lende, Smit R
Chanu, Sanjarambam Nirupama
Marak, Senrita Raksam
author_facet Katare, Milind B
Mogalekar, Havagiappa S
Swami, Aarti M
Singh, Mukesh K
Lende, Smit R
Chanu, Sanjarambam Nirupama
Marak, Senrita Raksam
Katare, Milind B
Mogalekar, Havagiappa S
Swami, Aarti M
Singh, Mukesh K
Lende, Smit R
Chanu, Sanjarambam Nirupama
Marak, Senrita Raksam
collection PubMed - marine biology
contents All-male production in Nile tilapia (Oreochromis niloticus) through discrete anastrozole immersion: hormonal and histological insights. Katare, Milind B Mogalekar, Havagiappa S Swami, Aarti M Singh, Mukesh K Lende, Smit R Chanu, Sanjarambam Nirupama Marak, Senrita Raksam Animals Male Anastrozole Cichlids Aromatase Inhibitors Testosterone Female Estradiol Generating all-male cohorts of Nile tilapia (Oreochromis niloticus) is commercially essential in modern aquaculture, as males exhibit substantially faster growth rates than females. Although oral delivery of the synthetic androgen 17α-methyltestosterone (MT) has long been the prevailing industry method for sex reversal, a range of practical and environmental shortcomings have fuelled the search for alternative strategies. The present study evaluated whether brief, repeated bath immersions in anastrozole, a third-generation, non-steroidal aromatase inhibitor, could reliably induce male sex reversal in Nile tilapia fry. Using a completely randomized design with five treatment levels (0, 1000, 1500, 2000, and 2500 µg/l anastrozole), each replicated three times, 3-day-old post-hatch fry were exposed to 3-h immersion sessions on days 3, 5, and 8 post-hatching, followed by a 120-day grow-out period. A clear and potent dose-dependent masculinizing effect was recorded; the 1500- and 2500-µg/l concentrations each yielded fully male populations (100%), as verified through phenotypic assessment, plasma hormone profiling, and gonadal histology. Aromatase inhibition was confirmed by marked reductions in circulating estradiol alongside significant increases in testosterone. Cortisol showed a transient, dose-dependent rise after the treatment window, yet post-treatment survival throughout the grow-out phase remained excellent, exceeding 98% and showing no statistically significant variation across groups. Histological evaluation revealed characteristic testicular architecture and atretic ovarian regression in all treated fish, in sharp contrast to the controls. The data collectively demonstrate that discrete anastrozole immersion represents an effective, operationally practical, and environmentally preferable alternative to conventional dietary hormone administration for all-male tilapia production.
format Artículo científico
id pubmed_42171893
institution PubMed
language en
publishDate 2026
publisher Fish physiology and biochemistry
record_format pubmed
spellingShingle All-male production in Nile tilapia (Oreochromis niloticus) through discrete anastrozole immersion: hormonal and histological insights.
Katare, Milind B
Mogalekar, Havagiappa S
Swami, Aarti M
Singh, Mukesh K
Lende, Smit R
Chanu, Sanjarambam Nirupama
Marak, Senrita Raksam
Animals
Male
Anastrozole
Cichlids
Aromatase Inhibitors
Testosterone
Female
Estradiol
All-male production in Nile tilapia (Oreochromis niloticus) through discrete anastrozole immersion: hormonal and histological insights. Katare, Milind B Mogalekar, Havagiappa S Swami, Aarti M Singh, Mukesh K Lende, Smit R Chanu, Sanjarambam Nirupama Marak, Senrita Raksam Animals Male Anastrozole Cichlids Aromatase Inhibitors Testosterone Female Estradiol Generating all-male cohorts of Nile tilapia (Oreochromis niloticus) is commercially essential in modern aquaculture, as males exhibit substantially faster growth rates than females. Although oral delivery of the synthetic androgen 17α-methyltestosterone (MT) has long been the prevailing industry method for sex reversal, a range of practical and environmental shortcomings have fuelled the search for alternative strategies. The present study evaluated whether brief, repeated bath immersions in anastrozole, a third-generation, non-steroidal aromatase inhibitor, could reliably induce male sex reversal in Nile tilapia fry. Using a completely randomized design with five treatment levels (0, 1000, 1500, 2000, and 2500 µg/l anastrozole), each replicated three times, 3-day-old post-hatch fry were exposed to 3-h immersion sessions on days 3, 5, and 8 post-hatching, followed by a 120-day grow-out period. A clear and potent dose-dependent masculinizing effect was recorded; the 1500- and 2500-µg/l concentrations each yielded fully male populations (100%), as verified through phenotypic assessment, plasma hormone profiling, and gonadal histology. Aromatase inhibition was confirmed by marked reductions in circulating estradiol alongside significant increases in testosterone. Cortisol showed a transient, dose-dependent rise after the treatment window, yet post-treatment survival throughout the grow-out phase remained excellent, exceeding 98% and showing no statistically significant variation across groups. Histological evaluation revealed characteristic testicular architecture and atretic ovarian regression in all treated fish, in sharp contrast to the controls. The data collectively demonstrate that discrete anastrozole immersion represents an effective, operationally practical, and environmentally preferable alternative to conventional dietary hormone administration for all-male tilapia production.
title All-male production in Nile tilapia (Oreochromis niloticus) through discrete anastrozole immersion: hormonal and histological insights.
topic Animals
Male
Anastrozole
Cichlids
Aromatase Inhibitors
Testosterone
Female
Estradiol
url https://pubmed.ncbi.nlm.nih.gov/42171893/