Impact of prolapse meshes on the metabolism of vaginal extracellular matrix in rhesus macaque.
Impact of prolapse meshes on the metabolism of vaginal extracellular matrix in rhesus macaque.
复制标题
脱垂网络对恒河猕猴阴道细胞外基质代谢的影响。
DOI:
10.1016/j.ajog.2014.08.008
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发表时间:
2015-02
影响因子:
9.8
通讯作者:
Moalli, Pamela A.
中科院分区:
文献类型:
--
作者:
Liang, Rui;Zong, Wenjun;Palcsey, Stacy;Abramowitch, Steven;Moalli, Pamela A.
The impact of polypropylene mesh implantation on vaginal collagen and elastin metabolism was analyzed using a nonhuman primate model to further delineate the mechanism of mesh induced complications. 49 middle aged parous rhesus macaques underwent surgical implantation of 3 synthetic meshes via sacrocolpopexy. Gynemesh PS (n=12) and two lower weight, higher porosity, lower stiffness meshes - UltraPro (n = 19) and Restorelle (n=8) were implanted, in which UltraPro was implanted with its blue orientation lines perpendicular (low stiffness direction, n=11) and parallel (high stiffness direction, n=8) to the longitudinal axis of vagina. Sham operated animals were used as controls (n=10). Twelve weeks after surgery, the meshtissue complex was excised and analyzed. Relative to Sham, Gynemesh PS had a negative impact on the metabolism of both collagen and elastin favoring catabolic reactions while UltraPro only induced an increase in elastin degradation. Restorelle had the least impact. As compared to Sham, the degradation of collagen and elastin in the vagina implanted with Gynemesh PS was increased with a simultaneous increase in active MMP-1, -8, -13 and total MMP-2, -9 (all P<0.05). The degradation of elastin (tropoelastin and mature elastin) was increased in the UltraPro implanted vagina with a concomitant increase of MMP-2, and -9 (all P<0.05). Collagen subtype ratio III/I was increased in both Gynemesh PS and UltraPro perpendicular groups (P<0.05). Following implantation with the heavier, less porous and stiffer mesh, Gynemesh PS, the degradation of vaginal collagen and elastin exceeded synthesis, most likely as a result of increased activity of MMPs, resulting in a structurally compromised tissue.
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影响因子:
2.8
作者:
Eriksen, HA;Pajala, A;Risteli, J
通讯作者:
Risteli, J
DOI:
10.1016/s0006-291x(76)80180-5
发表时间:
1976-01-01
影响因子:
3.1
作者:
SYKES, B;PUDDLE, B;SMITH, R
通讯作者:
SMITH, R
影响因子:
6
作者:
Drewes, Peter G.;Yanagisawa, Hiromi;Word, R. Ann
通讯作者:
Word, R. Ann
影响因子:
3.8
作者:
Niyibizi, C;Kavalkovich, K;Woo, SLY
通讯作者:
Woo, SLY
DOI:
10.1002/jbm.10119
发表时间:
2002-04-01
期刊:
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH
影响因子:
--
作者:
Klinge, U;Junge, K;Klosterhalfen, B
通讯作者:
Klosterhalfen, B