Skin fragility in obese diabetic mice: Possible involvement of elevated oxidative stress and upregulation of matrix metalloproteinases

Ai Ibuki, Tomoko Akase, Takashi Nagase, Takeo Minematsu, Gojiro Nakagami, Motoko Horii, Hiroshi Sagara, Takashi Komeda, Masayuki Kobayashi, Tsutomu Shimada, Masaki Aburada, Kotaro Yoshimura, Junko Sugama, Hiromi Sanada

研究成果: Article

33 引用 (Scopus)

抄録

The purpose of this study was to test the hypothesis that obese diabetic mice exhibit marked skin fragility, which is caused by increased oxidative stress and increased matrix metalloproteinase (MMP) gene expression in the subcutaneous adipose tissue. Scanning electron microscopy of skin samples from Tsumura-Suzuki obese diabetic (TSOD) mice revealed thinner collagen bundles, and decreased density and convolution of the collagen fibres. Furthermore, skin tensile strength measurements confirmed that the dorsal skin of TSOD mice was more fragile to tensile force than that of non-obese mice. The mRNA expressions of heme oxygenase 1 (Hmox1), a marker of oxidative stress, Mmp2 and Mmp14 were increased in the adipose tissue of TSOD mice. Antioxidant experiments were subsequently performed to determine whether the changes in collagen fibres and skin fragility were caused by oxidative stress. Strikingly, oral administration of the antioxidant dl-α-tocopherol acetate (vitamin E) decreased Hmox1, Mmp2 and Mmp14 mRNA expressions, and improved the skin tensile strength and structure of collagen fibres in TSOD mice. These findings suggest that the skin fragility in TSOD mice is associated with dermal collagen damage and weakened tensile strength, and that oxidative stress and MMP overexpression in the subcutaneous adipose tissue may, at least in part, affect dermal fragility via a paracrine pathway. These observations may contribute to novel clinical interventions, such as dietary supplementation with antioxidants or application of skin cream containing antioxidants, which may overcome skin fragility in obese patients with diabetes.

元の言語English
ページ(範囲)178-183
ページ数6
ジャーナルExperimental Dermatology
21
発行部数3
DOI
出版物ステータスPublished - 2012 3

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Oxidative stress
Matrix Metalloproteinases
Skin
Collagen
Antioxidants
Heme Oxygenase-1
Tensile strength
Tissue
Fibers
Skin Cream
Messenger RNA
alpha-Tocopherol
Medical problems
Vitamin E
Convolution
Gene expression
Scanning electron microscopy

ASJC Scopus subject areas

  • Dermatology
  • Molecular Biology
  • Biochemistry

これを引用

Skin fragility in obese diabetic mice : Possible involvement of elevated oxidative stress and upregulation of matrix metalloproteinases. / Ibuki, Ai; Akase, Tomoko; Nagase, Takashi; Minematsu, Takeo; Nakagami, Gojiro; Horii, Motoko; Sagara, Hiroshi; Komeda, Takashi; Kobayashi, Masayuki; Shimada, Tsutomu; Aburada, Masaki; Yoshimura, Kotaro; Sugama, Junko; Sanada, Hiromi.

:: Experimental Dermatology, 巻 21, 番号 3, 03.2012, p. 178-183.

研究成果: Article

Ibuki, A, Akase, T, Nagase, T, Minematsu, T, Nakagami, G, Horii, M, Sagara, H, Komeda, T, Kobayashi, M, Shimada, T, Aburada, M, Yoshimura, K, Sugama, J & Sanada, H 2012, 'Skin fragility in obese diabetic mice: Possible involvement of elevated oxidative stress and upregulation of matrix metalloproteinases', Experimental Dermatology, 巻. 21, 番号 3, pp. 178-183. https://doi.org/10.1111/j.1600-0625.2011.01409.x
Ibuki, Ai ; Akase, Tomoko ; Nagase, Takashi ; Minematsu, Takeo ; Nakagami, Gojiro ; Horii, Motoko ; Sagara, Hiroshi ; Komeda, Takashi ; Kobayashi, Masayuki ; Shimada, Tsutomu ; Aburada, Masaki ; Yoshimura, Kotaro ; Sugama, Junko ; Sanada, Hiromi. / Skin fragility in obese diabetic mice : Possible involvement of elevated oxidative stress and upregulation of matrix metalloproteinases. :: Experimental Dermatology. 2012 ; 巻 21, 番号 3. pp. 178-183.
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abstract = "The purpose of this study was to test the hypothesis that obese diabetic mice exhibit marked skin fragility, which is caused by increased oxidative stress and increased matrix metalloproteinase (MMP) gene expression in the subcutaneous adipose tissue. Scanning electron microscopy of skin samples from Tsumura-Suzuki obese diabetic (TSOD) mice revealed thinner collagen bundles, and decreased density and convolution of the collagen fibres. Furthermore, skin tensile strength measurements confirmed that the dorsal skin of TSOD mice was more fragile to tensile force than that of non-obese mice. The mRNA expressions of heme oxygenase 1 (Hmox1), a marker of oxidative stress, Mmp2 and Mmp14 were increased in the adipose tissue of TSOD mice. Antioxidant experiments were subsequently performed to determine whether the changes in collagen fibres and skin fragility were caused by oxidative stress. Strikingly, oral administration of the antioxidant dl-α-tocopherol acetate (vitamin E) decreased Hmox1, Mmp2 and Mmp14 mRNA expressions, and improved the skin tensile strength and structure of collagen fibres in TSOD mice. These findings suggest that the skin fragility in TSOD mice is associated with dermal collagen damage and weakened tensile strength, and that oxidative stress and MMP overexpression in the subcutaneous adipose tissue may, at least in part, affect dermal fragility via a paracrine pathway. These observations may contribute to novel clinical interventions, such as dietary supplementation with antioxidants or application of skin cream containing antioxidants, which may overcome skin fragility in obese patients with diabetes.",
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AU - Minematsu, Takeo

AU - Nakagami, Gojiro

AU - Horii, Motoko

AU - Sagara, Hiroshi

AU - Komeda, Takashi

AU - Kobayashi, Masayuki

AU - Shimada, Tsutomu

AU - Aburada, Masaki

AU - Yoshimura, Kotaro

AU - Sugama, Junko

AU - Sanada, Hiromi

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AB - The purpose of this study was to test the hypothesis that obese diabetic mice exhibit marked skin fragility, which is caused by increased oxidative stress and increased matrix metalloproteinase (MMP) gene expression in the subcutaneous adipose tissue. Scanning electron microscopy of skin samples from Tsumura-Suzuki obese diabetic (TSOD) mice revealed thinner collagen bundles, and decreased density and convolution of the collagen fibres. Furthermore, skin tensile strength measurements confirmed that the dorsal skin of TSOD mice was more fragile to tensile force than that of non-obese mice. The mRNA expressions of heme oxygenase 1 (Hmox1), a marker of oxidative stress, Mmp2 and Mmp14 were increased in the adipose tissue of TSOD mice. Antioxidant experiments were subsequently performed to determine whether the changes in collagen fibres and skin fragility were caused by oxidative stress. Strikingly, oral administration of the antioxidant dl-α-tocopherol acetate (vitamin E) decreased Hmox1, Mmp2 and Mmp14 mRNA expressions, and improved the skin tensile strength and structure of collagen fibres in TSOD mice. These findings suggest that the skin fragility in TSOD mice is associated with dermal collagen damage and weakened tensile strength, and that oxidative stress and MMP overexpression in the subcutaneous adipose tissue may, at least in part, affect dermal fragility via a paracrine pathway. These observations may contribute to novel clinical interventions, such as dietary supplementation with antioxidants or application of skin cream containing antioxidants, which may overcome skin fragility in obese patients with diabetes.

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