Vats Ravi, Ungalara Ramakrishna, Dubey Rikesh K, Sundd Prithu, Pradhan-Sundd Tirthadipa
Versiti Blood Research Institute and Blood Center of Wisconsin, 8733 West Watertown Plank Road, Milwaukee, WI 53226, USA.
Divisions of Cell Biology, Neurobiology and Anatomy and Bioengineering, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Cells. 2025 Jan 28;14(3):194. doi: 10.3390/cells14030194.
Pain constitutes a significant comorbidity associated with sickle cell disease (SCD). Analgesics serve as the primary method for pain management; however, the long-term effects of these drugs on the liver of SCD patients remain not completely understood. Using real-time intravital imaging, we analyzed the effect of non-steroidal analgesics (NSA) in the liver of control and SS (SCD) mice. Remarkably, we found completely opposing effects in the liver of control and SS mice post-NSA treatment. Whereas SS mice were able to better tolerate the NSA treatment acutely compared to their littermate controls, in the long term, these mice showed delayed resolution of liver injury and exacerbated fibrosis compared to control mice. Mechanistically, we found that SS mice were protected from cytotoxicity caused by NSA at baseline due to the significant activation of hepatic Kupffer cells, which produced heme-oxygenase 1 (HO-1). HO-1 promoted the activation of the cytoprotective enzyme Cyp3A11, which inhibited hepatic damage caused by NSA. However, in the long term, depletion of hepatic Kupffer cells led to reduced expression of HO-1, which blocked the activation of Cyp3A11, resulting in fibrosis and a delay in the resolution of liver injury and inflammation. These preclinical data provide a strong proof-of-concept for HO-1 as well as Cyp3A11 as cytoprotectors against NSA-induced liver damage in the Townes model of SCD and support further development of these compounds as potential novel therapies for end-organ damage in SCD.
疼痛是镰状细胞病(SCD)的一种重要合并症。镇痛药是疼痛管理的主要方法;然而,这些药物对SCD患者肝脏的长期影响仍未完全明确。我们利用实时活体成像技术,分析了非甾体类镇痛药(NSA)对对照小鼠和SS(SCD)小鼠肝脏的影响。值得注意的是,我们发现NSA治疗后,对照小鼠和SS小鼠的肝脏出现了完全相反的效应。与同窝对照小鼠相比,SS小鼠在急性情况下能够更好地耐受NSA治疗,但从长期来看,与对照小鼠相比,这些小鼠的肝损伤消退延迟且纤维化加剧。从机制上讲,我们发现由于肝库普弗细胞的显著激活,SS小鼠在基线时受到NSA引起的细胞毒性的保护,肝库普弗细胞产生血红素加氧酶1(HO-1)。HO-1促进了细胞保护酶Cyp3A11的激活,从而抑制了NSA引起的肝损伤。然而,从长期来看,肝库普弗细胞的耗竭导致HO-1表达减少,这阻碍了Cyp3A11的激活,导致纤维化以及肝损伤和炎症消退延迟。这些临床前数据为HO-1以及Cyp3A11作为SCD汤姆斯模型中对抗NSA诱导的肝损伤的细胞保护剂提供了有力的概念验证,并支持将这些化合物进一步开发为SCD终末器官损伤的潜在新疗法。