PMID- 33488313 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20210126 IS - 1559-3258 (Print) IS - 1559-3258 (Electronic) IS - 1559-3258 (Linking) VI - 18 IP - 4 DP - 2020 Oct-Dec TI - Protective Effect of S-Allyl Cysteine Against Neonatal Asthmatic Rats. PG - 1559325820982189 LID - 10.1177/1559325820982189 [doi] LID - 1559325820982189 AB - S-Allyl cysteine (SAC), an organic compound and a natural constituent of Allium sativum, commonly known as garlic have been consumed in routine foods are known to possess various biological activities. Nevertheless, scientific evidence on the protective effect of SAC against neonatal asthmatic rats is not available. Hence, the present study aimed at investigating the anti-asthmatic activity of SAC in neonatal asthmatic rats using Wistar rats. The study conducted in 4 groups consists of normal control rats, asthma-induced, asthma animals administered with SAC (25 mg/kg), and SAC control. At the end of the experimental period, inflammatory cells in bronchoalveolar lavage fluid (BALF), inflammatory markers, fibrinogen level, activated partial thromboplastin time, coagulation factor activity, and histopathology were elucidated. The current investigation exhibits that SAC significantly reduced the total leukocytes, with restored fibrinogen level, and activated partial thromboplastin time. In addition, the levels of inflammatory cytokines such as TNF-alpha (tumor necrosis factor- alpha), IL-6 (Interleukin 6), and IL-1beta have also attenuated in SAC treated animals. Furthermore, the mRNA expression levels of COX2 (cyclooxygenase-2), MCP-1 (monocyte chemoattractant protein-1), RANTES (regulated upon activation, normal T cell expressed and secreted), and eotaxin were reduced in SAC treated animals. Treatment of rats with SAC significantly reduced inflammation and eosinophil infiltration in the lungs. These results suggest that SAC exert protection in neonatal asthmatic rats suffering from acute or chronic inflammation by inducing anti-inflammatory and cell-protective responses. CI - (c) The Author(s) 2020. FAU - Jiang, Li AU - Jiang L AUID- ORCID: 0000-0001-9866-3950 AD - Department of Pediatrics, The First Hospital of Lanzhou University, Lanzhou, China. RINGGOLD: 117741 FAU - Li, Yuning AU - Li Y AD - Department of Pediatrics, The First Hospital of Lanzhou University, Lanzhou, China. RINGGOLD: 117741 FAU - Wang, Fang AU - Wang F AD - Department of Pediatrics, The First Hospital of Lanzhou University, Lanzhou, China. RINGGOLD: 117741 FAU - Zhang, Xindao AU - Zhang X AD - Department of Pediatrics, The First Hospital of Lanzhou University, Lanzhou, China. RINGGOLD: 117741 FAU - Zhao, Ruiping AU - Zhao R AD - Department of Pediatrics, The First Hospital of Lanzhou University, Lanzhou, China. RINGGOLD: 117741 LA - eng PT - Journal Article DEP - 20201224 PL - United States TA - Dose Response JT - Dose-response : a publication of International Hormesis Society JID - 101308899 PMC - PMC7768841 OTO - NOTNLM OT - S-allyl cysteine OT - inflammation OT - neonatal asthma COIS- Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. EDAT- 2021/01/26 06:00 MHDA- 2021/01/26 06:01 PMCR- 2020/12/24 CRDT- 2021/01/25 05:38 PHST- 2020/09/21 00:00 [received] PHST- 2020/11/16 00:00 [revised] PHST- 2020/11/26 00:00 [accepted] PHST- 2021/01/25 05:38 [entrez] PHST- 2021/01/26 06:00 [pubmed] PHST- 2021/01/26 06:01 [medline] PHST- 2020/12/24 00:00 [pmc-release] AID - 10.1177_1559325820982189 [pii] AID - 10.1177/1559325820982189 [doi] PST - epublish SO - Dose Response. 2020 Dec 24;18(4):1559325820982189. doi: 10.1177/1559325820982189. eCollection 2020 Oct-Dec.