The effects of camel milk in systemic inflammation and oxidative stress of cigarette smoke-induced chronic obstructive pulmonary disease model in rat
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作者:
Behrouz, Sepide
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Mashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Iran
Univ Birjand, Fac Agr, Dept Anim Sci, Birjand, IranMashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Iran
Behrouz, Sepide
[1
,2
]
Mohammadi, Mahla
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Mashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, IranMashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Iran
Mohammadi, Mahla
[1
]
Sarir, Hadi
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Univ Birjand, Fac Agr, Dept Anim Sci, Birjand, IranMashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Iran
Sarir, Hadi
[2
]
Boskabady, Mohammad Hossein
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Mashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Iran
Mashhad Univ Med Sci, Fac Med, Dept Physiol, Mashhad, IranMashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Iran
Boskabady, Mohammad Hossein
[1
,3
]
机构:
[1] Mashhad Univ Med Sci, Appl Biomed Res Ctr, Mashhad, Iran
[2] Univ Birjand, Fac Agr, Dept Anim Sci, Birjand, Iran
[3] Mashhad Univ Med Sci, Fac Med, Dept Physiol, Mashhad, Iran
Background The effects of camel milk in inflammation and systemic oxidative stress of cigarette smoke (CS)-induced chronic obstructive pulmonary disease (COPD) associated with small airway inflammation in rats were investigated. Methods 35 male Wistar rats were randomly divided into five groups: (a) control, (b) CS-exposed rats, c and (d) CS-exposed rats treated with the 4 and 8 mL/kg camel milk, and (e) CS-exposed rats treated with 1 mg/kg dexamethasone. Results Total and differential WBC counts, serum level of TNF-alpha and malondialdehyde (MDA) level in serum and homogenized tissues of the heart, kidney, liver, and testicle were significantly increased, but catalase (CAT), superoxide dismutase (SOD) and thiol levels were significantly decreased in CS-exposed rats (p < 0.01 to p < 0.001). Treatment with dexamethasone and both doses of camel milk improved all measured variables compared to the COPD group (p < 0.05 to p < 0.001). The improvements of most variables in the treated group with high dose of camel milk were higher than the effect of dexamethasone (p < 0.05 to p < 0.001). These findings suggest that camel milk has a therapeutic potential for treating systemic oxidative stress and inflammatory induced by CS. Conclusion Therefore, camel milk might be effective in attenuating the effects of CS-induced systemic inflammation and oxidative stress.
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Peking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R ChinaPeking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R China
Zhang, Lijiao
Li, Chunxiao
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Peking Univ Third Hosp, Dept Radiat Oncol, Beijing, Peoples R ChinaPeking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R China
Li, Chunxiao
Xiong, Jing
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Peking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R ChinaPeking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R China
Xiong, Jing
Chang, Chun
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Peking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R ChinaPeking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R China
Chang, Chun
Sun, Yongchang
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Peking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R ChinaPeking Univ Third Hosp, Dept Resp & Crit Care Med, Beijing, Peoples R China
机构:
Beijing Union Med Coll Hosp, Dept Resp Med, Peking Union Med Coll, Chinese Acad Med Sci, Beijing 100730, Peoples R ChinaBeijing Union Med Coll Hosp, Dept Resp Med, Peking Union Med Coll, Chinese Acad Med Sci, Beijing 100730, Peoples R China
Xu, L
Cai, BQ
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Beijing Union Med Coll Hosp, Dept Resp Med, Peking Union Med Coll, Chinese Acad Med Sci, Beijing 100730, Peoples R ChinaBeijing Union Med Coll Hosp, Dept Resp Med, Peking Union Med Coll, Chinese Acad Med Sci, Beijing 100730, Peoples R China
Cai, BQ
Zhu, YJ
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Beijing Union Med Coll Hosp, Dept Resp Med, Peking Union Med Coll, Chinese Acad Med Sci, Beijing 100730, Peoples R ChinaBeijing Union Med Coll Hosp, Dept Resp Med, Peking Union Med Coll, Chinese Acad Med Sci, Beijing 100730, Peoples R China
机构:
Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
Cui, Y. T.
Liang, Y. M.
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Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
Liang, Y. M.
Ip, M. S. M.
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Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
Univ Hong Kong, Res Ctr Heart Brain Hormone & Hlth Aging, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
Ip, M. S. M.
Mak, J. C. W.
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Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
Univ Hong Kong, Dept Pharmacol, Hong Kong, Hong Kong, Peoples R China
Univ Hong Kong, Res Ctr Heart Brain Hormone & Hlth Aging, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China