The tissue-specific nature of physiological zebrafish mitochondrial bioenergetics.
Rafael David Souto de AzevedoKivia Vanessa Gomes FalcãoSinara Monica Vitalino de AlmeidaMarlyete Chagas AraújoReginaldo Correia Silva-FilhoMaria Bernadete de Souza MaiaIan Porto Gurgel do AmaralAna Catarina Rezende LeiteRanilson de Souza BezerraPublished in: Mitochondrion (2024)
Zebrafish are a powerful tool to study a myriad of experimental conditions, including mitochondrial bioenergetics. Considering that mitochondria are different in many aspects depending on the tissue evaluated, in the zebrafish model there is still a lack of this investigation. Especially for juvenile zebrafish. In the present study, we examined whether different tissues from zebrafish juveniles show mitochondrial density- and tissue-specificity comparing brain, liver, heart, and skeletal muscle (SM). The liver and brain complex IV showed the highest O 2 consumption of all ETC in all tissues (10x when compared to other respiratory complexes). The liver showed a higher potential for ROS generation. In this way, the brain and liver showed more susceptibility to O 2 - generation when compared to other tissues. Regarding Ca 2+ transport, the brain showed greater capacity for Ca 2+ uptake and the liver presented low Ca 2+ uptake capacity. The liver and brain were more susceptible to producing NO. The enzymes SOD and Catalase showed high activity in the brain, whereas GPx showed higher activity in the liver and CS in the SM. TEM reveals, as expected, a physiological diverse mitochondrial morphology. The essential differences between zebrafish tissues investigated probably reflect how the mitochondria play a diverse role in systemic homeostasis. This feature may not be limited to normal metabolic functions but also to stress conditions. In summary, mitochondrial bioenergetics in zebrafish juvenile permeabilized tissues showed a tissue-specificity and a useful tool to investigate conditions of redox system imbalance, mainly in the liver and brain.
Keyphrases
- resting state
- white matter
- oxidative stress
- gene expression
- skeletal muscle
- cerebral ischemia
- functional connectivity
- heart failure
- multiple sclerosis
- type diabetes
- risk assessment
- reactive oxygen species
- brain injury
- adipose tissue
- metabolic syndrome
- deep learning
- subarachnoid hemorrhage
- mass spectrometry
- atrial fibrillation