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The DOI matches its Crossref record; 36 of the 36 references it cites were found in a registry or an index.

Visceral adipose tissue-derived serine protease inhibitor: A unique insulin-sensitizing adipocytokine in obesity

Open access
Hida, Kazuyuki, Wada, Jun, Eguchi, Jun, Zhang, Hong, Baba, Masako, Seida, Aya, Hashimoto, Izumi, Okada, Tatsuo, Yasuhara, Akihiro, Nakatsuka, Atsuko, Shikata, Kenichi, Hourai, Shinji, Futami, Junichiro, Watanabe, Eijiro, Matsuki, Yasushi, Hiramatsu, Ryuji, Akagi, Shigeru, Makino, Hirofumi, Kanwar, Yashpal S.·2005·Proceedings of the National Academy of Sciences

Abstract

There is a rapid global rise in obesity, and the link between obesity and diabetes remains somewhat obscure. We identified an adipocytokine, designated as visceral adipose tissue-derived serpin (vaspin), which is a member of serine protease inhibitor family. Vaspin cDNA was isolated by from visceral white adipose tissues (WATs) of Otsuka Long-Evans Tokushima fatty (OLETF) rat, an animal model of abdominal obesity with type 2 diabetes. Rat, mouse, and human vaspins are made up of 392, 394, and 395 amino acids, respectively; exhibit ≈40% homology with α 1 -antitrypsin; and are related to serine protease inhibitor family. Vaspin was barely detectable in rats at 6 wk and was highly expressed in adipocytes of visceral WATs at 30 wk, the age when obesity, body weight, and insulin levels peak in OLETF rats. The tissue expression of vaspin and its serum levels decrease with worsening of diabetes and body weight loss at 50 wk. The expression and serum levels were normalized with the treatment of insulin or insulin-sensitizing agent, pioglitazone, in OLETF rats. Administration of vaspin to obese CRL:CD-1 (ICR) (ICR) mice fed with high-fat high-sucrose chow improved glucose tolerance and insulin sensitivity reflected by normalized serum glucose levels. It also led to the reversal of altered expression of genes relevant to insulin resistance, e.g., leptin, resistin, TNFα, glucose transporter-4, and adiponectin. In DNA chip analyses, vaspin treatment resulted in the reversal of expression in ≈50% of the high-fat high-sucrose-induced genes in WATs. These findings indicate that vaspin exerts an insulin-sensitizing effect targeted toward WATs in states of obesity.

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Metadata

Authors
Hida, K., Wada, J., Eguchi, J., Zhang, H., Baba, M., Seida, A., Hashimoto, I., Okada, T., Yasuhara, A., Nakatsuka, A., Shikata, K., Hourai, S., Futami, J., Watanabe, E., Matsuki, Y., Hiramatsu, R., Akagi, S., Makino, H., & Kanwar, Y. S.
Venue
Proceedings of the National Academy of Sciences
Published
2005-07-19
Volume
102
Issue
30
Pages
10610-10615
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2105506930
Cited by
719
References
36
FWCI
12.43
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Visceral adipose tissue-derived serine protease inhibitor: A unique insulin-sensitizing adipocytokine in obesity. https://app.cochat.ai/papers/10.1073/pnas.0504703102
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Hida, K., Wada, J., Eguchi, J., Zhang, H., Baba, M., Seida, A., Hashimoto, I., Okada, T., Yasuhara, A., Nakatsuka, A., Shikata, K., Hourai, S., Futami, J., Watanabe, E., Matsuki, Y., Hiramatsu, R., Akagi, S., Makino, H., & Kanwar, Y. S. (2005). Visceral adipose tissue-derived serine protease inhibitor: A unique insulin-sensitizing adipocytokine in obesity. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.0504703102

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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