Autor: |
KUWAHARA, Naota, YAMAGUCHI, Munehiro, TANAKA, Akihiko, OHTA, Shin, UNO, Tomoki, UCHIDA, Yoshitaka, MANABE, Ryo, JINNO, Megumi, HIRAI, Kuniaki, MIYATA, Yoshito, MIZUMA, Hiroko, HOMMA, Tetsuya, YAMAMOTO, Mayumi, YAMAGUCHI, Fumihiro, KUSUMOTO, Sojiro, SUZUKI, Shintaro, OHNISHI, Tsukasa, SAGARA, Hironori |
Jazyk: |
angličtina |
Rok vydání: |
2019 |
Předmět: |
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Zdroj: |
The Showa University journal of medical sciences. 31(1):1-12 |
ISSN: |
0915-6380 |
Popis: |
Chlorella extract (CE) has been shown to induce production of T helper-1 cytokines, and regulate serum IgE levels in animal models of asthma. We aimed to evaluate whether CE could inhibit ovalbumin (OVA)-induced airway hyperresponsiveness (AHR) and airway remodeling in a murine model of asthma. Balb/c mice were allocated to four groups: a control group (no OVA exposure, not given CE), a CE group (no OVA exposure, given CE), an asthma group (sensitized/challenged with OVA, not given CE) and a CE+asthma group (sensitized/challenged with OVA, given CE). In the asthma and CE+asthma groups, mice were sensitized with OVA on day 0 and day 12, and then challenged with OVA on three consecutive days. In the CE and CE+asthma groups, the mice were given feed containing 2% CE. We assessed AHR to methacholine, and analyzed bronchoalveolar lavage fluid (BALF), serum, lung tissue and spleen cells. Administration of CE was associated with significantly lower AHR in OVA-sensitized and challenged mice. CE administration was also associated with marked reduction of total cells, eosinophils and T helper-2 cytokines (IL-4, IL-5 and IL-13) in BALF. In addition, administration of CE significantly decreased the numbers of periodic acid-Schiff (PAS)-positive cells in OVA-sensitized and challenged mice. Administration of CE also directly suppressed IL-4, IL-5 and IL-13 production in spleen cells of OVA-sensitized and challenged mice. These results indicate that CE can partly prevent AHR and airway remodeling in a murine model of asthma. |
Databáze: |
OpenAIRE |
Externí odkaz: |
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