# Effects of L-Ornithine-L-Aspartate on Angiogenesis and Perfusion in Subacute Hind Limb Ischemia: Preliminary Study

**Authors:** Sanghoon Jung, Ye Jin Park, Jiwon Jeon, Kyuseok Kim

PMC · DOI: 10.3390/biomedicines12081787 · Biomedicines · 2024-08-06

## TL;DR

This study shows that L-Ornithine-L-Aspartate improves blood flow and new blood vessel growth in rats with leg artery blockage.

## Contribution

The study is the first to document LOLA's effect on angiogenesis and perfusion recovery in subacute hind limb ischemia.

## Key findings

- LOLA treatment significantly increased perfusion in ischemic limbs.
- LOLA led to higher CD31-positive capillary density and VEGF overexpression.
- Perfusion improvements were observed during the subacute phase of HLI.

## Abstract

The current treatment options for peripheral arterial disease (PAD) are limited due to a lack of significant high-level evidence to inform clinical decisions and unfavorable outcomes in terms of cost-effectiveness and amputation rates. In order to suggest the use of the commercially available L-Ornithine-L-Aspartate (LOLA) for treating PAD, we induced hind limb ischemia (HLI) by unilaterally ligating the femoral artery in a rat model. The rats were randomly divided into three groups, with seven rats assigned to each group: group 1 (control), group 2 (sorbitol), and group 3 (LOLA). Intraperitoneal injections were administered five times on post-operative days (PODs) 3, 5, 7, 10, and 12. Perfusion imaging was conducted on PODs 7 and 14 and compared to pre-operative perfusion imaging. Immunohistochemistry staining and Western blotting were performed after the final perfusion imaging. Group 3 showed a significant increase in perfusion, high CD31-positive capillary lumen density, and substantial overexpression of VEGF in the ischemic limb during the subacute phase of HLI. In conclusion, this study provides the first documented evidence of angiogenesis and perfusion recovery in the subacute phase of the HLI model following the administration of LOLA. With LOLA readily available on the commercial market, the implementation of LOLA treatment for PAD in humans can be expedited compared to other therapies still in the developmental stage.

## Linked entities

- **Proteins:** VEGFA (vascular endothelial growth factor A)
- **Chemicals:** L-Ornithine-L-Aspartate (PubChem CID 10220941), sorbitol (PubChem CID 5780)
- **Diseases:** peripheral arterial disease (MONDO:0005386)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Pecam1 (platelet and endothelial cell adhesion molecule 1) [NCBI Gene 29583] {aka CD31, Pecam}, Vegfa (vascular endothelial growth factor A) [NCBI Gene 83785] {aka VEGF-A, VEGF111, VEGF164, VPF, Vegf}
- **Diseases:** ischemic (MESH:D002545), PAD (MESH:D058729), HLI (MESH:D007511)
- **Chemicals:** sorbitol (MESH:D013012), L-Ornithine-L-Aspartate (MESH:C002939)
- **Species:** Homo sapiens (human, species) [taxon 9606], Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11351382/full.md

## References

68 references — full list in the complete paper: https://tomesphere.com/paper/PMC11351382/full.md

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Source: https://tomesphere.com/paper/PMC11351382