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Simvastatin and atorvastatin reduce the mechanical properties of tendon constructs in vitro and introduce catabolic changes in the gene expression pattern

Eliasson, Pernilla, 1982- (författare)
Linköpings universitet,Avdelningen för Kirurgi, Ortopedi och Onkologi,Medicinska fakulteten,Bispebjerg Hospital, Denmark; University of Copenhagen, Denmark
Svensson, Rene B. (författare)
Bispebjerg Hospital, Denmark; University of Copenhagen, Denmark
Giannopoulos, Antonis (författare)
Bispebjerg Hospital, Denmark; University of Copenhagen, Denmark
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Eismark, Christian (författare)
Bispebjerg Hospital, Denmark; University of Copenhagen, Denmark
Kjaer, Michael (författare)
Bispebjerg Hospital, Denmark; University of Copenhagen, Denmark
Schjerling, Peter (författare)
Bispebjerg Hospital, Denmark; University of Copenhagen, Denmark
Heinemeier, Katja M. (författare)
Bispebjerg Hospital, Denmark; University of Copenhagen, Denmark
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 (creator_code:org_t)
2017-03-06
2017
Engelska.
Ingår i: PLOS ONE. - : PUBLIC LIBRARY SCIENCE. - 1932-6203. ; 12:3
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Treatment with lipid-lowering drugs, statins, is common all over the world. Lately, the occurrence of spontaneous tendon ruptures or tendinosis have suggested a negative influence of statins upon tendon tissue. But how statins might influence tendons is not clear. In the present study, we investigated the effect of statin treatment on mechanical strength, cell proliferation, collagen content and gene expression pattern in a tendon-like tissue made from human tenocytes in vitro. Human tendon fibroblasts were grown in a 3D tissue culture model (tendon constructs), and treated with either simvastatin or atorvastatin, low or high dose, respectively, for up to seven days. After seven days of treatment, mechanical testing of the constructs was performed. Collagen content and cell proliferation were also determined. mRNA levels of several target genes were measured after one or seven days. The maximum force and stiffness were reduced by both statins after 7 days (pamp;lt;0.05), while the cross sectional area was unaffected. Further, the collagen content was reduced by atorvastatin (p = 0.01) and the cell proliferation rate was decreased by both types of statins (pamp;lt;0.05). Statin treatment also introduced increased mRNA levels of MMP-1, MMP-3, MMP-13, TIMP-1 and decreased levels of collagen type 1 and 3. In conclusion, statin treatment appears to have a negative effect on tendon matrix quality as seen by a reduced strength of the tendon constructs. Further, activated catabolic changes in the gene expression pattern and a reduced collagen content indicated a disturbed balance in matrix production of tendon due to statin administration.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)

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