Cumhur Cure Medine, Cure Erkan
Department of Biochemistry, Private Tanfer Hospital, Istanbul 34394, Turkey.
Department of Internal Medicine, Bagcilar Medilife Hospital, Istanbul 34200, Turkey.
World J Virol. 2023 Jan 25;12(1):12-21. doi: 10.5501/wjv.v12.i1.12.
The liver has many significant functions, such as detoxification, the urea cycle, gluconeogenesis, and protein synthesis. Systemic diseases, hypoxia, infections, drugs, and toxins can easily affect the liver, which is extremely sensitive to injury. Systemic infection of severe acute respiratory syndrome coronavirus 2 can cause liver damage. The primary regulator of intracellular pH in the liver is the Na/H exchanger (NHE). Physiologically, NHE protects hepatocytes from apoptosis by making the intracellular pH alkaline. Severe acute respiratory syndrome coronavirus 2 increases local angiotensin II levels by binding to angiotensin-converting enzyme 2. In severe cases of coronavirus disease 2019, high angi-otensin II levels may cause NHE overstimulation and lipid accumulation in the liver. NHE overstimulation can lead to hepatocyte death. NHE overstimulation may trigger a cytokine storm by increasing proinflammatory cytokines in the liver. Since the release of proinflammatory cytokines such as interleukin-6 increases with NHE activation, the virus may indirectly cause an increase in fibrinogen and D-dimer levels. NHE overstimulation may cause thrombotic events and systemic damage by increasing fibrinogen levels and cytokine release. Also, NHE overstimulation causes an increase in the urea cycle while inhibiting vitamin D synthesis and gluconeogenesis in the liver. Increasing NHE3 activity leads to Na loading, which impairs the containment and fluidity of bile acid. NHE overstimulation can change the gut microbiota composition by disrupting the structure and fluidity of bile acid, thus triggering systemic damage. Unlike other tissues, tumor necrosis factor-alpha and angiotensin II decrease NHE3 activity in the intestine. Thus, increased luminal Na leads to diarrhea and cytokine release. Severe acute respiratory syndrome coronavirus 2-induced local and systemic damage can be improved by preventing virus-induced NHE overstimulation in the liver.
肝脏具有许多重要功能,如解毒、尿素循环、糖异生和蛋白质合成。全身性疾病、缺氧、感染、药物和毒素很容易影响肝脏,肝脏对损伤极为敏感。严重急性呼吸综合征冠状病毒2的全身感染可导致肝损伤。肝脏细胞内pH值的主要调节因子是钠/氢交换体(NHE)。生理上,NHE通过使细胞内pH值呈碱性来保护肝细胞免于凋亡。严重急性呼吸综合征冠状病毒2通过与血管紧张素转换酶2结合来增加局部血管紧张素II水平。在2019冠状病毒病的严重病例中,高血管紧张素II水平可能导致NHE过度刺激和肝脏脂质蓄积。NHE过度刺激可导致肝细胞死亡。NHE过度刺激可能通过增加肝脏中的促炎细胞因子引发细胞因子风暴。由于白细胞介素-6等促炎细胞因子的释放随NHE激活而增加,病毒可能间接导致纤维蛋白原和D-二聚体水平升高。NHE过度刺激可能通过增加纤维蛋白原水平和细胞因子释放导致血栓形成事件和全身损伤。此外,NHE过度刺激会导致尿素循环增加,同时抑制肝脏中的维生素D合成和糖异生。增加NHE3活性会导致钠负荷增加,从而损害胆汁酸的容纳和流动性。NHE过度刺激可通过破坏胆汁酸的结构和流动性来改变肠道微生物群组成,从而引发全身损伤。与其他组织不同,肿瘤坏死因子-α和血管紧张素II会降低肠道中的NHE3活性。因此,管腔内钠增加会导致腹泻和细胞因子释放。通过防止病毒诱导的肝脏NHE过度刺激,可以改善严重急性呼吸综合征冠状病毒2引起的局部和全身损伤。