Key result
Vascopoietin administration in a mouse model of posterior limb ischemia restored blood flow, decreased necrosis size, and reduced amputation frequency.
Why the study?
Does Vascopoietin (HGF and angiopoietin-1 plasmids) improve blood flow and reduce necrosis in ischemic tissues?
Does Vascopoietin (HGF and angiopoietin-1 plasmids) improve blood flow and reduce necrosis in ischemic tissues?
Vascopoietin, a plasmid construct expressing HGF and angiopoietin-1, successfully promotes therapeutic angiogenesis and restores blood flow in preclinical models of limb ischemia.
Hypothesis-generating for plasmid-based angiogenesis in limb ischemia; human trials required before clinical consideration.
New methods to stimulate blood supply of the ischemic organs and tissues are being intensively developed worldwide. These approaches are based on revascularization and remodeling of the newly formed blood vessels. This strategy was called therapeutic angiogenesis. Using in vitro, ex vivo and in vivo models we investigated the specific biological activity and angiogenic potential of Vascopoietin, which contained the plasmids for HGF and angiopoietin-1 expression. Vascopoietin stimulated vascular cell migration, proliferation and the formation of capillary-like structures in vitro and ex vivo. Using in vivo model of posterior limb ischemia in mice we demonstrated that Vascopoietin administration mediated stable HGF and angiopoietin-1 production resulting in new blood vessel formation and their stabilization in the ischemic muscles. In addition, Vascopoietin injection led to the restoration of the blood flow, decrease in the size of necrosis in ischemic limb and the reduction in the amputation frequency. The current data suggest Vascopoietin a promising drug for therapeutic angiogenesis.
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Rubina et al. (2018) studied Posterior limb ischemia. Vascopoietin (plasmids for HGF and angiopoietin-1) was evaluated on Restoration of blood flow, decrease in necrosis size, and reduction in amputation frequency. Vascopoietin administration in a mouse model of posterior limb ischemia restored blood flow, decreased necrosis size, and reduced amputation frequency.
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