Molecular Insight into Acute Limb Ischemia

Author:

Costa Davide12ORCID,Ielapi Nicola123ORCID,Perri Paolo4,Minici Roberto5ORCID,Faga Teresa6,Michael Ashour6,Bracale Umberto Marcello7ORCID,Andreucci Michele6ORCID,Serra Raffaele12ORCID

Affiliation:

1. Department of Medical and Surgical Sciences, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy

2. Interuniversity Center of Phlebolymphology (CIFL), “Magna Graecia” University, 88100 Catanzaro, Italy

3. Department of Public Health and Infectious Disease, “Sapienza” University of Rome, 00185 Rome, Italy

4. Department of Vascular and Endovascular Surgery, Annunziata Hospital, 1 Via Migliori, 87100 Cosenza, Italy

5. Department of Experimental and Clinical Medicine, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy

6. Department of Health Sciences, Magna Graecia University of Catanzaro, 88100 Catanzaro, Italy

7. Department of Public Health, University Federico II of Naples, 80131 Naples, Italy

Abstract

Acute limb ischemia (ALI) is defined as a sudden reduction in blood flow to a limb, resulting in cessation of blood flow and, therefore, cessation of the delivery of nutrients and oxygen to the tissues of the lower limb. Despite optimal treatment to restore blood flow to ischemic tissues, some patients may suffer from ischemia/reperfusion (I/R) syndrome, the most severe complication after a revascularization procedure used to restore blood flow. There are multiple molecular and cellular factors that are involved in each phase of ALI. This review focuses firstly on molecular and cellular factors of arterial thrombosis, highlighting the role of atherosclerotic plaques, smooth muscle cells (SMCs), and cytokine which may alter key components of the extracellular matrix (ECM). Then, molecular and cellular factors of arterial embolism will be discussed, highlighting the importance of thrombi composition. Molecular and cellular factors of ischemia/reperfusion syndrome are analyzed in depth, highlighting several important mechanisms related to tissue damage, such as inflammation, apoptosis, autophagy, necrosis, and necroptosis. Furthermore, local and general complications of ALI are discussed in the context of molecular alterations. Ultimately, the role of novel biomarkers and targeted therapies is discussed.

Publisher

MDPI AG

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