脯氨酸对高盐下缢蛏线粒体稳态与能量代谢的影响

Effects of proline on mitochondrial homeostasis and energy metabolism in the razor clam (Sinonovacula constricta) under high salinity stress

  • 摘要:
    目的 研究脯氨酸对高盐下缢蛏线粒体稳态及能量代谢的影响。
    方法 本实验设置对照组、高盐组及外源脯氨酸组,通过对缢蛏鳃组织超微结构的观察、线粒体动态平衡相关基因的表达(pinkparkinsirtopamnf2、ampkfis),以及能量代谢相关酶(PK、MDH、SDH、LDH)活性的测定,以期了解脯氨酸对提高缢蛏高盐耐受性能的作用。
    结果 高盐胁迫下缢蛏线粒体结构出现明显损伤,线粒体膜溶解、嵴断裂消失,空泡化等现象加剧;添加脯氨酸后线粒体面积与空泡率在胁迫48和72 h均显著低于对照组。高盐胁迫下,pinkparkin表达量先升后降,峰值分别在48、24 h,而添加脯氨酸组则持续上升,96 h显著高于高盐组;sirt基因表达量在高盐胁迫条件48 h时开始上升、72 h达峰值,而添加脯氨酸组12 h即显著上升且持续;ampk基因表达量在高盐组先升后降,外源脯氨酸组与其趋势一致但12 h峰值更高;opamnf2在高盐组在48 h达到峰值,而脯氨酸组则持续上升,且显著高于高盐组;fis基因表达量在高盐胁迫条件下先升后降,24 h达到最大值,添加脯氨酸组趋势相同但表达量显著更低。高盐胁迫条件下PK、MDH、SDH酶活性先升高后下降的趋势,而LDH活性与之相反;在添加脯氨酸组中,一定程度上增加了PK、MDH和SDH活性,显著高于高盐组,而LDH活性则显著低于高盐组。
    结论 脯氨酸能够稳定高盐胁迫下线粒体的结构,并且通过线粒体动态平衡来调节线粒体的数量和质量,缓解线粒体在高盐下的损伤,同时改善了高盐胁迫条件下有氧代谢水平,提高缢蛏的耐高盐性能。

     

    Abstract: Extreme weather events are increasingly exacerbating salinity fluctuations in estuarine and intertidal zones, posing a serious threat to the habitat stability of benthic bivalves. These rapid and unpredictable salinity changes disrupt osmotic balance and impair critical physiological functions, often resulting in high mortality rates in natural populations and substantial economic losses in aquaculture. The razor clam Sinonovacula constricta, as an economically important bivalve species, is particularly susceptible to severe damage under sudden salinity shifts. Previous studies have shown that exogenous proline, acting as an osmolyte, can alleviate tissue damage and oxidative stress induced by high salinity, thereby enhancing the hyperosmotic tolerance of S. constricta. To investigate the protective role of exogenous proline in mitochondrial homeostasis and energy metabolism of S. constricta under high salinity stress, three experimental groups were established that a control group, a high-salinity group, and exogenous proline group. The study evaluated the ultrastructure of gill tissue, expression levels of key mitochondrial dynamics-related genes (pink, parkin, sirt, opa, mnf2, ampk, fis), and activities of energy metabolism enzymes (PK, MDH, SDH, LDH). Results revealed that high salinity induced severe mitochondrial damage, including membrane dissolution, cristae fragmentation, and vacuolization. Following proline supplementation, the mitochondrial area and vacuolization rate at both 48 h and 72 h of stress were significantly lower than those in the control group. Gene expression analysis showed that under high salinity stress, pink and parkin expression initially increased and then decreased, peaking at 48 h and 24 h, respectively. In contrast, the exogenous proline group sustained higher expression levels, significantly exceeding those of the high salinity group at 96 h. The sirt gene exhibited upregulation starting at 48 h under high salinity, peaking at 72 h, while proline treatment triggered a significant and continuous increase from 12 h onward. ampk expression showed a transient increase under high salinity, with an earlier and higher peak at 12 h in the proline group. opa and mnf2 expression peaked at 48 h under high salinity, but continued to rise in the exogenous proline group, ending significantly higher. fis expression was also upregulated initially under salinity stress, peaking at 24 h, but remained significantly lower in the exogenous proline group. Enzymatically, high salinity led to an initial increase followed by a decline in PK, MDH, and SDH activities, while LDH activity showed the opposite trend. Proline supplementation enhanced PK, MDH, and SDH activities and suppressed LDH activity, indicating a shift toward improved aerobic metabolism. In conclusion, proline stabilizes mitochondrial structure, regulates mitochondrial dynamics and quality control, promotes efficient energy production, and enhances high salinity tolerance in S. constricta.

     

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