Acta Veterinaria Brno

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• Li Wenyang, Li Hongxu, Fei Fan, Gao Xiaoqiang, Cao Shuquan, Li Wensheng, Jin Bo, Liu Baoliang: Analysis of correlation between daily rhythm of digestion and metabolism of grouper (Epinephelus lanceolatus\u2642\u2009×\u2009Epinephelus fuscoguttatus\u2640) and water quality parameters in recycling aquaculture system. Aquacult Int 2025, 33. <https://doi.org/10.1007/s10499-024-01706-x>
• Farias Caio Francisco Santana, Ventura Arlene Sobrinho, Jerônimo Gabriela Tomas, Cardoso Claudia Andrea Lima, de Matos Lorena Vieira, da Silva Grazyelle Sebrenski, Gonçalves Ligia Uribe, Povh Jayme Aparecido, Martins Maurício Laterça: Pharmacokinetics and metabolism of basil (Ocimum basilicum) essential oil as an anesthetic for tambaqui (Colossoma macropomum). Aquacult Int 2024, 32, 2923. <https://doi.org/10.1007/s10499-023-01304-3>
• Öz Mustafa, Inanan Burak Evren, Karasahin Tahir, Dikel Suat: Effects of glutamine on growth performance, nutrient content, fatty acid profile, and blood parameters of rainbow trout (Oncorhynchus mykiss). Journal of Fish Biology 2024, 104, 1213. <https://doi.org/10.1111/jfb.15666>
• Retcheski Milena Cia, Maximowski Luiz Vitor, Escorsin Keveen Jhonathan Soares, de Almeida Rosa Kurosaki Jéssica Kimie, Romão Silvia, Bitencourt Thiago Bergler, Parra Jorge Erick Garcia, Cazarolli Luisa Helena: Yarrowia lipolytica biomass—a potential additive to boost metabolic and physiological responses of Nile tilapia. Fish Physiol Biochem 2023, 49, 655. <https://doi.org/10.1007/s10695-023-01219-z>
• Jahanbani Alireza, Shahriari Ali, Mohammadian Takavar: Ureagenesis of Asian seabass (Lates calcarifer) under ammonia stress and overcrowding. Aquaculture 2023, 576, 739810. <https://doi.org/10.1016/j.aquaculture.2023.739810>
• Mwaura John Gitau, Wekesa Clabe, Ogutu Philip A., Okoth Patrick: Whole Transcriptome Analysis of Differentially Expressed Genes in Cultured Nile Tilapia (O. niloticus) Subjected to Chronic Stress Reveals Signaling Pathways Associated with Depressed Growth. Genes 2023, 14, 795. <https://doi.org/10.3390/genes14040795>
• Crane Adam L., Bairos‐Novak Kevin R., Goldman Jack A., Brown Grant E.: Chemical disturbance cues in aquatic systems: a review and prospectus. Ecological Monographs 2022, 92. <https://doi.org/10.1002/ecm.1487>
• Xu Hao, Ren Mingchun, Liang Hualiang, Ge Xianping, Ji Ke, Huang Dongyu, Yu Heng, Wu Longhua: Interactive effects of water salinity and dietary methionine levels on growth performance, whole-body composition, plasma parameters, and expression of major nutrient metabolism genes in juvenile genetically improved farmed Tilapia (Oreochromis niloticus). Aquaculture 2022, 546, 737381. <https://doi.org/10.1016/j.aquaculture.2021.737381>
• Hidalgo M. Carmen, Morales Amalia E., Pula Héctor J., Tomás-Almenar Cristina, Sánchez-Muros M. José, Melenchón Federico, Fabrikov Dmitri, Cardenete Gabriel: Oxidative metabolism of gut and innate immune status in skin and blood of tench (Tinca tinca) fed with different insect meals (Hermetia illucens and Tenebrio molitor). Aquaculture 2022, 558, 738384. <https://doi.org/10.1016/j.aquaculture.2022.738384>
• Espinoza‐Ramos Luis A., Pepe‐Victoriano Renzo, Huanacuni Jordan I., Nande Manuel: Effect of transportation time and stocking density on seawater quality and survival of Anisotremus scapularis (Perciformes: Haemulidae). J World Aquaculture Soc 2022, 53, 1042. <https://doi.org/10.1111/jwas.12865>
• Dhal Sambandh Bhusan, Jungbluth Kyle, Lin Raymond, Sabahi Seyed Pouyan, Bagavathiannan Muthukumar, Braga-Neto Ulisses, Kalafatis Stavros: A Machine-Learning-Based IoT System for Optimizing Nutrient Supply in Commercial Aquaponic Operations. Sensors 2022, 22, 3510. <https://doi.org/10.3390/s22093510>
• Novotny Ladislav: Respiratory Tract Disorders in Fishes. Veterinary Clinics of North America: Exotic Animal Practice 2021, 24, 267. <https://doi.org/10.1016/j.cvex.2021.01.001>
• Pikula Jiri, Pojezdal Lubomir, Papezikova Ivana, Minarova Hana, Mikulikova Ivana, Bandouchova Hana, Blahova Jana, Bednarska Małgorzata, Mares Jan, Palikova Miroslava: Carp Edema Virus Infection Is Associated With Severe Metabolic Disturbance in Fish. Front. Vet. Sci. 2021, 8. <https://doi.org/10.3389/fvets.2021.679970>
• Barca Sandra, Vieira-Lanero Rufino, Nachón David José, Sánchez-Hernández Javier, Cobo María del Carmen, Cobo Fernando: Complexity of the Relationship between Environmental Factors, Interspecific Competition, and Intrinsic Traits of the Species in Explaining the Invasive Success of Gobio lozanoi Doadrio & Madeira, 2004. Water 2021, 13, 3043. <https://doi.org/10.3390/w13213043>
• Zhang Huan, Sun Gaigai, Lin Zhihua, Yao Hanhan, Dong Yinghui: The razor clam Sinonovacula constricta uses the strategy of conversion of toxic ammonia to glutamine in response to high environmental ammonia exposure. Mol Biol Rep 2020, 47, 9579. <https://doi.org/10.1007/s11033-020-06018-w>
• Xu Chenyuan, Liu Wenbin, Zhang Dingdong, Liu Jiadai, Zheng Xiaochuan, Zhang Caiyan, Yao Jianguo, Zhu Chongmiao, Chi Cheng: Effects of partial fish meal replacement with two fermented soybean meals on the growth of and protein metabolism in the Chinese mitten crab (Eriocheir sinensis). Aquaculture Reports 2020, 17, 100328. <https://doi.org/10.1016/j.aqrep.2020.100328>
• Vaclavik Josef, Sehonova Pavla, Hodkovicova Nikola, Vecerkova Lenka, Blahova Jana, Franc Ales, Marsalek Petr, Mares Jan, Tichy Frantisek, Svobodova Zdenka, Faggio Caterina: The effect of foodborne sertraline on rainbow trout (Oncorhynchus mykiss). Science of The Total Environment 2020, 708, 135082. <https://doi.org/10.1016/j.scitotenv.2019.135082>
• Dinda Riya, Mandal Amit, Das S. K.: Neem (Azadirachta indica A. Juss) supplemented biofloc medium as alternative feed in common carp (Cyprinus carpio var. communis Linnaeus) culture. Journal of Applied Aquaculture 2020, 32, 361. <https://doi.org/10.1080/10454438.2019.1645076>
• Alam Muhammad Shoaib, Liang Xu‐Fang, Liu Liwei, He Shan, Liu Yong, Li Jiao: Effect of dietary protein‐to‐energy ratios on growth performance, body composition, feed utilization and nitrogen metabolism enzyme of Cirrhinus mrigala. Aquac Res 2020, 51, 5056. <https://doi.org/10.1111/are.14844>
• Hodkovicova N, Mares J, Sehonova P, Blahova J, Faldyna M, Modra H, Tichy F, Caha J, Vrankova A, Svobodova Z: The effect of a sudden temperature decrease on selected physiological indices in the common carp. Vet. Med. 2020, 65, 346. <https://doi.org/10.17221/67/2020-VETMED>
• Lin Ching-Yu, Huang Lu-Hsueh, Deng Dong-Fang, Lee Sheng-Han, Liang Hao-Jan, Hung Silas S.O.: Metabolic adaptation to feed restriction on the green sturgeon (Acipenser medirostris) fingerlings. Science of The Total Environment 2019, 684, 78. <https://doi.org/10.1016/j.scitotenv.2019.05.044>
• dos Santos Silva Márcio José, da Costa Franklin Fernando Batista, Leme Fabiola Paes, Takata Rodrigo, Costa Deliane Cristina, Mattioli Cristiano Campos, Luz Ronald Kennedy, Miranda-Filho Kleber Campos: Biological responses of Neotropical freshwater fish Lophiosilurus alexandri exposed to ammonia and nitrite. Science of The Total Environment 2018, 616-617, 1566. <https://doi.org/10.1016/j.scitotenv.2017.10.157>
• Shi Xiao-chen, Jin Ai, Sun Jian, Tian Jing-jing, Ji Hong, Chen Li-qiao, Du Zhen-yu: The protein-sparing effect of α-lipoic acid in juvenile grass carp, Ctenopharyngodon idellus: effects on lipolysis, fatty acid β-oxidation and protein synthesis. Br J Nutr 2018, 120, 977. <https://doi.org/10.1017/S000711451800226X>
• Zhou J.S., Chen H.J., Ji H., Shi X.C., Li X.X., Chen L.Q., Du Z.Y., Yu H.B.: Effect of dietary bile acids on growth, body composition, lipid metabolism and microbiota in grass carp (Ctenopharyngodon idella). Aquacult Nutr 2018, 24, 802. <https://doi.org/10.1111/anu.12609>
• Barreto-Curiel Fernando, Focken Ulfert, D’Abramo Louis R., Viana María Teresa, Motta Andrea: Metabolism of Seriola lalandi during Starvation as Revealed by Fatty Acid Analysis and Compound-Specific Analysis of Stable Isotopes within Amino Acids. PLoS ONE 2017, 12, e0170124. <https://doi.org/10.1371/journal.pone.0170124>
• Czerniak Ewa, Gomułka Piotr, Dągowski Jakub: Influence of 1-phenoxy-2-propanol on blood profile of common carp. Acta Vet. Brno 2017, 86, 133. <https://doi.org/10.2754/avb201786020133>
• Vargas-Chacoff Luis, Ruiz-Jarabo Ignacio, Arjona Francisco J., Laiz-Carrión Raúl, Flik Gert, Klaren Peter H.M., Mancera Juan M.: Energy metabolism of hyperthyroid gilthead sea bream Sparus aurata L. Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 2016, 191, 25. <https://doi.org/10.1016/j.cbpa.2015.09.014>
• Min Eun-Young, Kim Shin-Hu, Hwang In-Ki, Kim Kyeong-Wook, Park Bo-Mi, Lee Jung Sick, Kang Ju-Chan: Influence of elevated temperatures on the physiological response of hemolymph from two species of abalone, Haliotis gigantea and Haliotis discus discus (Reeve, 1846). The Korean Journal of Malacology 2015, 31, 187. <https://doi.org/10.9710/kjm.2015.31.3.187>
• Emadi Shaibani Mina, Mojazi Amiri Bagher, Khodabandeh Saber: Starvation and refeeding effects on pyloric caeca structure of Caspian salmon (Salmo trutta caspius, Kessler 1877) juvenile. Tissue and Cell 2013, 45, 204. <https://doi.org/10.1016/j.tice.2013.01.001>
• Adamec Jiri, Jannasch Amber, Höök Tomas O., Nalepa Thomas, Gribskov Michael, Sepúlveda Maria S., Maity Suman: Metabolite Profiles in Starved Diporeia spp. Using Liquid Chromatography-Mass Spectrometry (LC-MS) Based Metabolomics. Journal of Crustacean Biology 2012, 32, 239. <https://doi.org/10.1163/193724011X615578>
• Caruso G., Maricchiolo G., Micale V., Genovese L., Caruso R., Denaro M. G.: Physiological responses to starvation in the European eel (Anguilla anguilla): effects on haematological, biochemical, non-specific immune parameters and skin structures. Fish Physiol Biochem 2010, 36, 71. <https://doi.org/10.1007/s10695-008-9290-6>
• Stegeman Nadia, Heatley J. Jill, Rodrigues Aline, Pool Roy: Nephroblastoma in a Koi (Cyprinus carpio). Journal of Exotic Pet Medicine 2010, 19, 298. <https://doi.org/10.1053/j.jepm.2010.10.009>
• Żarski Daniel, Kucharczyk Dariusz, Targońska Katarzyna, Krejszeff Sławomir, Czarkowski Tomasz, Babiarz Ewelina, Nowosielska Dorota: Dynamics of nitrogen and phosphorus in closed and semi-closed recirculating aquaculture systems during the intensive culture of goldfish, Carassius auratus auratus (L.), juveniles. Archives of Polish Fisheries 2010, 18. <https://doi.org/10.2478/v10086-010-0022-z>
• Sripadi Prabhakar, Nazarian Javad, Hathout Yetrib, Hoffman Eric P., Vertes Akos: In vitro analysis of metabolites from the untreated tissue of Torpedo californica electric organ by mid-infrared laser ablation electrospray ionization mass spectrometry. Metabolomics 2009, 5, 263. <https://doi.org/10.1007/s11306-008-0147-x>
• Madison B. N., Dhillon R. S., Tufts B. L., Wang Y. S.: Exposure to low concentrations of dissolved ammonia promotes growth rate in walleye Sander vitreus. Journal of Fish Biology 2009, 74, 872. <https://doi.org/10.1111/j.1095-8649.2008.02165.x>
• Carneiro Paulo César Falanghe, Swarofsky Elaine Correa, Souza Daniana Pinotti E., César Thiago Mocelin Ramos, Baglioli Bárbara, Baldisserotto Bernardo: Ammonia‐, Sodium Chloride‐, and Calcium Sulfate‐induced Changes in the Stress Responses of Jundiá, Rhamdia quelen, Juveniles. J World Aquaculture Soc 2009, 40, 810. <https://doi.org/10.1111/j.1749-7345.2009.00302.x>
• Dobšíková R., Svobodová Z., Bláhová J., Modrá H., Velíšek J.: The effect of transport on biochemical and haematological indices of common carp (Cyprinus carpio L.). Czech J. Anim. Sci. 2009, 54, 510. <https://doi.org/10.17221/52/2009-CJAS>
• Svobodová Zdeňka, Máchová Jana, Kroupová Hana, Smutná Miriam, Groch Ladislav: Ammonia autointoxication of common carp: case studies. Aquacult Int 2007, 15, 277. <https://doi.org/10.1007/s10499-007-9079-0>
• Le François N. R., Savoie A., Siikavuopio S. I.: Gill metabolic and osmoregulatory responses of juvenile Atlantic cod (Gadus morhua) to chronic ammonia exposure. J Appl Ichthyol 2007, 0, 071018043205008. <https://doi.org/10.1111/j.1439-0426.2007.01012.x>
• Boudreaux Perry J., Ferrara Allyse M., Fontenot Quenton C.: Acute Toxicity of Ammonia to Spotted Gar, Lepisosteus oculatus, Alligator Gar, Atractosteus spatula, and Paddlefish, Polyodon spathula. J World Aquaculture Soc 2007, 38, 322. <https://doi.org/10.1111/j.1749-7345.2007.00104.x>
• Miller Todd W.: Tissue-specific response of δ15N in adult Pacific herring (Clupea pallasi) following an isotopic shift in diet. Environ Biol Fish 2006, 76, 177. <https://doi.org/10.1007/s10641-006-9020-9>
• Das P.C., Ayyappan S., Jena J.K.: Haematological changes in the three Indian major carps, Catla catla (Hamilton), Labeo rohita (Hamilton) and Cirrhinus mrigala (Hamilton) exposed to acidic and alkaline water pH. Aquaculture 2006, 256, 80. <https://doi.org/10.1016/j.aquaculture.2006.02.019>
• Stinefelt Beth M., Eya Jonathan C., Semmens Kenneth J., Blemings Kenneth P.: Effect of Diet and Strain on Growth and Performance in Hybrid Bluegills. N American J Aquac 2004, 66, 312. <https://doi.org/10.1577/A03-069.1>