Interference of doxycycline pretreatment in a model of abdominal aortic aneurysms

Cardiovasc Pathol. 2015 Mar-Apr;24(2):110-20. doi: 10.1016/j.carpath.2014.10.004. Epub 2014 Nov 5.

Abstract

Background: Abdominal aortic aneurysm (AAA) is characterized by chronic inflammation and degradation of the extracellular matrix, mediated by matrix metalloproteinases (MMPs). Doxycycline has been reported to control the progression of AAA by regulation of MMP. We hypothesized that doxycycline pretreatment in a rat model of AAA would cause reduction in gelatinolytic activity of MMP-2 and -9 and the inflammatory response in the wall of an aneurysm, consequently decreasing the formation and development of AAAs.

Methods: Male Wistar rats were divided into the following four groups: aneurysm (A); control (C); aneurysm+doxycycline (A+D) and control+doxycycline (C+D), with 24 animals per group subdivided into n=6 animals at different time points [1, 3, 7, and 15 days postsurgery (dps)]. The (A) and (A+D) groups simultaneously received the injury and extrinsic stenosis of the aortic wall. The (C) and (C+D) groups received sham operation. The treated animals received doxycycline via gavage (30 mg/kg/day) from 48 h before surgery until the end of experiment. At 1, 3, 7, and 15 dps, the animals were euthanized, and the aortas were collected for morphological analyses, immunohistochemistry, and zymography.

Results: The animals from the (A) group developed AAAs. However, the animals treated with doxycycline showed a 85% decrease in AAA development, which was associated with a large reduction in gelatinolytic activity of MMP-2 and -9, and decreased inflammatory response (P<.05).

Conclusions: These results suggest that pretreatment with doxycycline before surgery inhibited the activity of MMP-2 and -9, as well as the inflammatory response, and may play an important role in the prevention of the development of AAAs.

Keywords: Abdominal aortic aneurysm; Doxycycline pretreatment; Inflammatory response; Metalloproteinases 2 and 9.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aorta, Abdominal / drug effects*
  • Aorta, Abdominal / enzymology
  • Aortic Aneurysm, Abdominal / enzymology
  • Aortic Aneurysm, Abdominal / pathology*
  • Disease Models, Animal
  • Doxycycline / pharmacology*
  • Enzyme Inhibitors / pharmacology*
  • Immunohistochemistry
  • Inflammation / enzymology
  • Inflammation / pathology
  • Male
  • Matrix Metalloproteinase 2 / metabolism
  • Matrix Metalloproteinase 9 / metabolism
  • Rats
  • Rats, Wistar

Substances

  • Enzyme Inhibitors
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9
  • Doxycycline