Matrix Metalloproteinase Inhibitors Attenuate Neuroinflammation Following Focal Cerebral Ischemia in Mice

Cheol Hong Park; Tae Kyeong Shin; Ho Youn Lee; So Jung Kim; Won Suk Lee

doi:10.4196/kjpp.2011.15.2.115

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Park, Shin, Lee, Kim, and Lee: Matrix Metalloproteinase Inhibitors Attenuate Neuroinflammation Following Focal Cerebral Ischemia in Mice

Original Article

Korean J Physiol Pharmacol 2011;15(2):115-122.

Published online: 18 February 2011

DOI: https://doi.org/10.4196/kjpp.2011.15.2.115

Matrix Metalloproteinase Inhibitors Attenuate Neuroinflammation Following Focal Cerebral Ischemia in Mice

Cheol Hong Park, Tae Kyeong Shin, Ho Youn Lee, So Jung Kim, Won Suk Lee

Department of Pharmacology, and Medical Research Center for Ischemic Tissue Regeneration, Pusan National University School of Medicine, Yangsan 626-870, Korea

Corresponding to: Won Suk Lee, Department of Pharmacology, and Medical Research Center for Ischemic Tissue Regeneration, Pusan National University School of Medicine, Beomeo-ri, Mulgeum-eup, Yangsan 626-870, Korea. (Tel) 82-51-510-8062, (Fax) 82-51-510-8068, (E-mail) wonslee@pusan.ac.kr

Received 10 April 2011 Revised 19 April 2011 Accepted 20 April 2011

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

The aim of this study was to investigate whether matrix metalloproteinase (MMP) inhibitors attenuate neuroinflammation in an ischemic brain following photothrombotic cortical ischemia in mice. Male C57BL/6 mice were anesthetized, and Rose Bengal was systemically administered. Permanent focal ischemia was induced in the medial frontal and somatosensory cortices by irradiating the skull with cold white light. MMP inhibitors, such as doxycycline, minocycline, and batimastat, significantly reduced the cerebral infarct size, and the expressions of monocyte chemotactic protein-1 (MCP-1), tumor necrosis factor-α (TNF-α), and indoleamine 2,3-dioxygenase (IDO). However, they had no effect on the expressions of heme oxygenase-1 and neuroglobin in the ischemic cortex. These results suggest that MMP inhibitors attenuate ischemic brain injury by decreasing the expression levels of MCP-1, TNF-α, and IDO, thereby providing a therapeutic benefit against cerebral ischemia.

Keywords: Matrix metalloproteinase inhibitor, Monocyte chemotactic protein-1, Tumor necrosis factor-α, Indoleamine 2,3-dioxygenase, Photothrombotic cortical ischemia

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Fig. 1.

Effects of doxycycline and minocycline on infarct area (left panels) and volume (right panels) in mice. Animals were treated with doxycycline (20 mg/kg, s.c.) or minocycline (45 mg/kg, s.c.) 30 min before and 2 h after ischemic insult, and were sacrificed 24 h after photothrombotic cortical ischemia. The numbers in parentheses indicate the numbers of animals. ^∗p<0.05, ^∗∗p<0.01 vs. vehicle group.

Fig. 2.

Effect of matrix metalloproteinase (MMP) inhibitors on expression of monocyte chemotactic protein-1 (MCP-1) in ischemic cerebral cortex after photothrombotic cortical ischemia in mice. Doxycycline (20 mg/kg) or minocycline (45 mg/kg) was administered s.c. 30 min before and 2 h after ischemic insult, and batimastat (50 mg/kg) was administered i.p. 30 min before ischemic insult. The animals were sacrificed 24 h after photothrombotic cortical ischemia. Four animals were used in each group. Scale bar=50 μm. ^∗∗p<0.01, ^∗∗∗p<0.001 vs. vehicle group.

Fig. 3.

Effect of MMP inhibitors on expression of tumor necrosis factor-α (TNF-α) in ischemic cerebral cortex after photothrombotic cortical ischemia in mice. Animals were treated with doxycycline (20 mg/kg) or minocycline (45 mg/kg) s.c. 30 min before and 2 h after ischemic insult, or with batimastat (50 mg/kg) i.p. 30 min before ischemic insult, and were sacrificed 24 h after photothrombotic cortical ischemia. Three animals were used in each group. Scale bar= 50 μm. ^∗∗p<0.01, ^∗∗∗p<0.001 vs. vehicle group.

Fig. 4.

Effect of MMP inhibitors on expression of indoleamine 2,3-dioxygenase (IDO) in ischemic cerebral cortex after photothrombotic cortical ischemia in mice. Animals were treated with doxycycline (20 mg/kg) or minocycline (45 mg/kg) s.c. 30 min before and 2 h after ischemic insult, or with batimastat (50 mg/kg) i.p. 30 min before ischemic insult, and were sacrificed 24 h after photothrombotic cortical ischemia. Numbers in columns indicate the numbers of animals. Scale bar=50 μm. ^∗∗p<0.01, ^∗∗∗p<0.001 vs. vehicle group.

Fig. 5.

Effect of MMP inhibitors on expression of heme oxygenase-1 (HO-1) in ischemic cerebral cortex after photothrombotic cortical ischemia in mice. Animals were treated with doxycycline (20 mg/kg) or minocycline (45 mg/kg) s.c. 30 min before and 2 h after ischemic insult, or with batimastat (50 mg/kg) i.p. 30 min before ischemic insult, and were sacrificed 24 h after photothrombotic cortical ischemia. Numbers in columns indicate the numbers of animals. Scale bar=50 μm.

Fig. 6.

Effect of MMP inhibitors on expression of neuroglobin (Ngb) in the ischemic cerebral cortex after photothrombotic cortical ischemia in mice. Animals were treated with doxycycline (20 mg/kg) or minocycline (45 mg/kg) s.c. 30 min before and 2 h after ischemic insult, or with batimastat (50 mg/kg) i.p. 30 min before ischemic insult, and were sacrificed 24 h after photothrombotic cortical ischemia. Numbers in columns indicate the numbers of animals. Scale bar=50 μm.

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