Abstract
Background: More than one-quarter of Americans have hypercholesterolemia and/or are being treated with cholesterol-lowering medications. Given the systemic nature of hypercholesterolemia and remaining questions regarding its effect on tendons at a local level, we sought to assess the utility of small versus large animal model systems for translational studies by exploring the effect of hypercholesterolemia on supraspinatus tendon elastic mechanical properties in mice, rats, and monkeys. We hypothesized that stiffness and elastic modulus would be increased in tendons across species due to hypercholesterolemia. Materials and methods: Supraspinatus tendons from normal (control) and high-cholesterol (HC) mice, rats, and monkeys were used in this study. After dissection, tendons were geometrically measured and tensile tested with tissue strain measured optically. Results: Overall, HC animals had significantly altered plasma lipid profiles. Biomechanical testing showed a significant increase in stiffness compared with control in HC mice and rats, as well as a nonsignificant trend for HC monkeys. Elastic modulus was also significantly increased in HC mice and monkeys, with HC rats showing a trend. Conclusions: The consistency of our findings across species and between small and large animals, combined with the fact that the aged mice were exposed to lifelong hypercholesterolemia (compared with rats and nonhuman primates, which were fed HC diets), suggests that these increased properties may be inherent to the effect of hypercholesterolemia on supraspinatus tendon rather than due to an effect of cumulative exposure time to the effects of HC. Further investigation is needed to confirm this concept.
| Original language | English |
|---|---|
| Pages (from-to) | 681-686 |
| Number of pages | 6 |
| Journal | Journal of Shoulder and Elbow Surgery |
| Volume | 22 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 2013 |
Funding
The authors, their immediate families, and any research foundations with which they are affiliated have not received any financial payments or other benefits from any commercial entity related to the subject of this article. The mouse component of this work was supported by a grant from the American Orthopaedic Society for Sports Medicine to J.A. Abboud. The rat component was funded by the Orthopaedic Research and Education Foundation to J.A. Abboud. Other funding, including support of D.P. Beason, was provided by the National Institutes of Health (NIH)–National Institute of Arthritis and Musculoskeletal and Skin Diseases ( P30 AR050950 to L.J. Soslowsky). Additional support for the nonhuman primate work was provided by a pathway-to-independence grant from the NIH–National Heart, Lung, and Blood Institute ( K99/R00-HL088528 to R.E. Temel). A.L. McDaniel was supported by a training grant from the NIH–National Heart, Lung, and Blood Institute ( T32-HL091797 ).
| Funders | Funder number |
|---|---|
| National Institutes of Health (NIH) | |
| National Heart, Lung, and Blood Institute (NHLBI) | K99/R00-HL088528, T32HL091797 |
| National Institute of Arthritis and Musculoskeletal and Skin Diseases | P30 AR050950 |
| Orthopaedic Research and Education Foundation | |
| American Orthopaedic Society for Sports Medicine |
Keywords
- Animal model
- Biomechanics
- Hypercholesterolemia
- Rotator cuff
- Shoulder
- Tendon
ASJC Scopus subject areas
- Surgery
- Orthopedics and Sports Medicine
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