Table 4. Common animal models for evaluation of artificial blood vessels in vivo.
Animal model | Characteristics | Application inner diameter (mm) | Common length (mm) | Longest implantation period | Implantation site | References |
---|---|---|---|---|---|---|
Sheep | Similar cardiovascular physiology, endothelialisation mechanisms and thrombogenicity mechanisms to humans. Suitable size and long-term studies possible. Higher incidence of hypercoagulability. |
4-6 4-6 |
80-100 60-100 |
9 months 3 months |
Carotid artery Arteriovenous graft |
48, 74 129 |
Pig | Similar vascular physiology and anatomy to humans. Well established as a model for assessing vascular grafts. Mount an extensive immune response to implanted tissues. |
3-6 3-6 |
30-100 10-100 |
6 months 4 weeks |
Iliac artery Carotid artery |
130
52 |
Dog | Lack of spontaneous endothelialisation and immune response restricts study lengths. Ease of accessing vessel due to thin skin. Thrombogenicity mechanisms and vessel viscoelastic properties differ from humans. |
3-6 3-6 |
30-50 30-50 |
6 months 1 year |
Abdominal artery Carotid artery |
131
119 |
Baboon | Physiology and cardiovascular anatomy are the most similar to humans. Suitable for a wide range of non-invasive imaging techniques adapted from humans. High cost and ethical concerns associated with using primates in medical research. |
3-6 | 30-50 | 6 months | Arteriovenous graft | 26 |
Rabbit | Similar endothelialisation rates and thrombogenicity mechanisms to humans. Demanding higher anticoagulant function. Limited to short-term studies. |
1-4 1-4 1-4 |
5-30 5-30 5-30 |
12 months 2 weeks 3 months |
Carotid artery Femoral artery Abdominal artery |
94, 132 133 134 |
Rat | Large sample size. Wide variety of transgenic lines. Allows exploration of genetic/molecular mechanisms. |
1-3 1-3 |
5-30 5-10 |
18 months 12 weeks |
Abdominal artery Carotid artery |
73, 135 136 |
Mouse | Ideal for biocompatibility and cell infiltration studies. | 0.5-1 | 3-10 | 6 months | Carotid artery | 137 |