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The alpha-lipoic acid derivative DHLHZn: a new therapeutic agent for acute lung injury in vivo
Authors:Yoshiaki Shoji  Hiroya Takeuchi  Kazumasa Fukuda  Koichi Fukunaga  Rieko Nakamura  Tsunehiro Takahashi  Norihito Wada  Hirofumi Kawakubo  Taku Miyasho  Takahiro Hiratsuka  Masafumi Inomata  Tomoko Betsuyaku  Yuko Kitagawa
Affiliation:1.Department of Surgery, School of Medicine,Keio University,Shinjuku-Ku,Japan;2.Department of Surgery, School of Medicine,Hamamatsu University, Hamamatsu,Japan;3.Division of Pulmonary Medicine, Department of Medicine, School of Medicine,Keio University,Shinjuku-Ku,Japan;4.Department of Veterinary Science, School of Veterinary Medicine,Rakuno Gakuen University,Ebetsu,Japan;5.Department of Gastroenterological and Pediatric Surgery, Faculty of Medicine,Oita University,Yufu-Shi,Japan
Abstract:

Objective and design

An animal experiment was performed to demonstrate the anti-inflammatory effects of an alpha-lipoic acid (ALA) derivative, dihydrolipoyl histidinate zinc complex (DHLHZn) for acute lung injury (ALI) and to investigate the mechanism of action.

Material

Rats were randomly divided into three experimental groups: control group (n = 17), DHLHZn(?) group (n = 11, ALI model rats), and DHLHZn(+) group (n = 12, ALI model rats treated by DHLHZn).

Treatment

Lipopolysaccharides (LPS, 10 mg/kg) were administered intratracheally in the DHLHZn(?) group and the DHLHZn(+) group. For the DHLHZn(+) group, DHLHZn (100 mg/kg) was administered intraperitoneally 2 h prior to LPS administration.

Methods

Four hours after LPS administration, bronchoalveolar lavage fluid (BALF) and lung tissue were collected. The findings were analyzed using the Mann–Whitney U test.

Results

Total number of cells, number of neutrophils and lymphocytes, levels of various inflammatory cytokines, and NF-kB p65 concentration of BALF were significantly lower in the DHLHZn(+) group than in the DHLHZn(?) group (p < 0.05). ALI pathology scores were significantly lower in the DHLHZn(+) group than in the DHLHZn(?) group (p < 0.001).

Conclusions

Anti-inflammatory effects of DHLHZn for ALI were demonstrated by BALF and histopathological findings. The mechanism of action of DHLHZn was considered to be via inhibition of the NF-kB signaling pathway. DHLHZn is thus suggested to be a new prophylactic agent for ALI.
Keywords:
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