Univ. Littoral Côte d'Opale, USC ANSES, EA 7394 - ICV - Institut Charles Viollette, F-62200 Boulogne-sur-Mer, France; Univ. Lille, F-59000 Lille, France; Univ. Artois, F-62000 Arras, France; INRA, French National Institute for Agricultural Research, France; ISA, F-59000 Lille, France.
Univ. Bordeaux, INSERM U1045, IHU-LIRYC, F-33600 Pessac, France.
Food Chem. 2019 Jul 30;287:38-45. doi: 10.1016/j.foodchem.2019.02.076. Epub 2019 Feb 23.
The current methods used to routinely assess freshness in the fishing industry reflect more a state of spoilage than a state of freshness. Mitochondria, the seat of cellular respiration, undergo profound changes in post mortem tissues. The objective of this study was to demonstrate that mitochondrial activity constitutes a putative early fish freshness marker. The structure of gilthead sea bream (Sparus aurata) muscle tissue was evaluated over time by transmission electron microscopy. Respiration was assessed in mitochondria isolated from sea bream fillets using oxygraphy. Membrane potential (ΔΨ) was determined by fluorescence (Rhodamine 123). Mitochondrial activity of fillets stored at +4 °C was studied for 6 days. Changes in mitochondrial cristae structure appeared from Day 3 highlighting the presence of dense granules. ΔΨ and mitochondrial activity were significantly disrupted in sea bream fillets after 96 h of storage at +4 °C. Mitochondrial activity constituted a reliable and early indicator of fish freshness.
当前用于渔业常规评估新鲜度的方法更多地反映了变质状态,而不是新鲜状态。线粒体是细胞呼吸的场所,在死后组织中会发生深刻的变化。本研究的目的是证明线粒体活性是一种潜在的早期鱼类新鲜度标志物。通过透射电子显微镜评估了真鲷(Sparus aurata)肌肉组织的结构。使用耗氧法评估了从真鲷鱼片分离的线粒体中的呼吸作用。通过荧光(Rhodamine 123)测定膜电位(ΔΨ)。研究了在+4°C下储存 6 天的鱼片的线粒体活性。从第 3 天开始,线粒体嵴结构的变化出现,突出了致密颗粒的存在。在+4°C下储存 96 小时后,真鲷鱼片的ΔΨ和线粒体活性明显受到破坏。线粒体活性是鱼类新鲜度的可靠和早期指标。