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罗氟司特在脓毒症中的心血管效应:风险还是获益?

Cardiovascular effects of Roflumilast during sepsis: Risks or benefits?

机构信息

Department of Pharmacology, Federal University of Santa Catarina, Florianópolis, Brazil; Department of Neurosciences "Rita Levi Montalcini", University of Turin, Turin, Italy.

Department of Pharmacology, Federal University of Santa Catarina, Florianópolis, Brazil.

出版信息

Eur J Pharmacol. 2024 Nov 15;983:177015. doi: 10.1016/j.ejphar.2024.177015. Epub 2024 Sep 26.

Abstract

BACKGROUND

Phosphodiesterase-4 (PDE4) is responsible for terminating cyclic adenosine monophosphate (cAMP) signalling. PDE4 inhibitors, such as roflumilast (RFM), have anti-inflammatory activity and have been studied in inflammation-induced tissue damage in sepsis. However, the role of RFM on cardiovascular derangements induced by sepsis is still unknown. Thus, we aimed to evaluate the potential effects of RFM on cardiovascular collapse and multiorgan damage caused by sepsis.

METHODS

Sepsis was induced by cecal ligation and puncture (CLP) in male rats. Six hours after the CLP or sham procedure, animals were randomly assigned to receive either RFM (0.3 mg/kg) or vehicle subcutaneously, and cardiovascular parameters were assessed 24 h after the surgery and organ/plasma samples were collected for further analyses.

RESULTS

Sepsis induced hypotension, tachycardia, reduced renal blood flow (RBF) and hyporeactivity to vasoconstrictors both in vivo and ex vivo. RFM treatment increased systemic cAMP levels and RBF. RFM also attenuated hypoperfusion and liver damage induced by CLP. Furthermore, RFM reduced systemic nitric oxide (NO) levels in septic rats, while there were no changes in hepatic NOS-2 expression. Nevertheless, RFM exacerbated sepsis-induced hypotension and tachycardia without ameliorating vascular hyporeactivity.

CONCLUSION

Our data show that PDE-4 inhibition protects septic rats from hepatic injury and improves renal perfusion. However, RFM worsened hemodynamic parameters and showed no protection against sepsis-induced cardiovascular dysfunction and mortality. Thus, despite the anti-inflammatory benefits of RFM, its application in sepsis should be approached cautiously.

摘要

背景

磷酸二酯酶 4(PDE4)负责终止环磷酸腺苷(cAMP)信号转导。PDE4 抑制剂,如罗氟司特(RFM),具有抗炎活性,并已在脓毒症引起的炎症性组织损伤中进行了研究。然而,RFM 对脓毒症引起的心血管紊乱的作用尚不清楚。因此,我们旨在评估 RFM 对脓毒症引起的心血管衰竭和多器官损伤的潜在影响。

方法

通过盲肠结扎和穿刺(CLP)在雄性大鼠中诱导脓毒症。CLP 或假手术后 6 小时,动物随机接受皮下给予 RFM(0.3mg/kg)或载体,并在手术后 24 小时评估心血管参数,并收集器官/血浆样本进行进一步分析。

结果

脓毒症导致低血压、心动过速、肾血流量(RBF)减少以及体内和体外对血管收缩剂的反应性降低。RFM 治疗增加了全身 cAMP 水平和 RBF。RFM 还减轻了 CLP 引起的低灌注和肝损伤。此外,RFM 降低了脓毒症大鼠的全身一氧化氮(NO)水平,而肝 NOS-2 表达没有变化。然而,RFM 加重了脓毒症引起的低血压和心动过速,而没有改善血管低反应性。

结论

我们的数据表明,PDE-4 抑制可保护脓毒症大鼠免受肝损伤,并改善肾脏灌注。然而,RFM 恶化了血流动力学参数,对脓毒症引起的心血管功能障碍和死亡率没有保护作用。因此,尽管 RFM 具有抗炎作用,但在脓毒症中的应用应谨慎。

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