PMID- 32913716 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240407 IS - 2214-7500 (Electronic) IS - 2214-7500 (Linking) VI - 7 DP - 2020 TI - Neuroprotective effect of Costus afer on low dose heavy metal mixture (lead, cadmium and mercury) induced neurotoxicity via antioxidant, anti-inflammatory activities. PG - 1032-1038 LID - 10.1016/j.toxrep.2020.08.008 [doi] AB - Humans are constantly exposed to heavy metals due to their ubiquity in the environment. Hence, this study investigated the possible protective effect of Costus afer aqueous leaf extract (CALE) against low dose heavy metal mixture (LDHMM)-induced neurotoxicity. Male albino rats were divided into 6 equal groups. Group 1 served as the normal control receiving only deionized water. Group 2 served as the toxic control receiving on metal mixture (20 mg/kg PbCl(2), 1.61 mg/kg CdCl(2) and 0.40 mg/kg HgCl(2)), groups 3, 4 and 5 were co-treated with metal mixture and CALE (750, 1500 and 2250 mg/kg body weight, respectively) and group 6 was treated with metal mixture and ZnCl(2). All treatments were administered through oral gavage for 90days. Oxidative stress biomarkers [malondialdehyde (MDA), superoxide dismutase (SOD), glutathione content (GSH) and catalase (CAT)], inflammatory cytokines [interlukin-6 (IL-6) and interlukin-10 (IL-10)], histopathological changes and heavy metal concentration were determined in brain of rats. Results indicated that LDHMM significantly increased (p < 0.05) the lipid peroxidation marker (MDA) and the pro-inflammatory cytokine (IL-6), while lowered levels of the oxidative biomarkers (SOD, CAT and GSH) and anti-inflammatory cytokine (IL-10). Also, LDHMM caused some histopathological changes such as reactive gliosis and glia cell proliferation. LDHMM elevated the lead, cadmium and mercury concentrations in the brain. Severity of the distorted cortical parameters were ameliorated by CALE administration. The CALE induced significant protective effect on LDHMM-mediated neurotoxicity in a dose-dependent manner which may be a result of its antioxidant anti-inflammatory and metal chelation mechanisms. CI - (c) 2020 The Authors. FAU - Anyanwu, Brilliance O AU - Anyanwu BO AD - African Centre of Excellence for Oilfield Chemicals Research (ACE-CEFOR), University of Port Harcourt, PMB, 5323 Port Harcourt, Choba, Nigeria. FAU - Orish, Chinna N AU - Orish CN AD - Department of Anatomy, Faculty of Basic Medical Sciences, College of Health Sciences, University of Port Harcourt, PMB, 5323 Port Harcourt, Choba, Nigeria. FAU - Ezejiofor, Anthonet N AU - Ezejiofor AN AD - African Centre of Excellence for Public Health and Toxicological Research (ACE-PUTOR), University of Port Harcourt, PMB, 5323 Port Harcourt, Choba, Nigeria. FAU - Nwaogazie, Ify L AU - Nwaogazie IL AD - African Centre of Excellence for Oilfield Chemicals Research (ACE-CEFOR), University of Port Harcourt, PMB, 5323 Port Harcourt, Choba, Nigeria. FAU - Orisakwe, Orish E AU - Orisakwe OE AD - African Centre of Excellence for Public Health and Toxicological Research (ACE-PUTOR), University of Port Harcourt, PMB, 5323 Port Harcourt, Choba, Nigeria. LA - eng PT - Journal Article DEP - 20200815 PL - Ireland TA - Toxicol Rep JT - Toxicology reports JID - 101630272 PMC - PMC7472923 OTO - NOTNLM OT - Costus afer OT - Heavy metal exposure OT - Metal chelation OT - Neurotoxicity OT - Oxidative stress COIS- The authors report no declarations of interest. EDAT- 2020/09/12 06:00 MHDA- 2020/09/12 06:01 PMCR- 2020/08/15 CRDT- 2020/09/11 05:45 PHST- 2020/03/24 00:00 [received] PHST- 2020/04/24 00:00 [revised] PHST- 2020/08/10 00:00 [accepted] PHST- 2020/09/11 05:45 [entrez] PHST- 2020/09/12 06:00 [pubmed] PHST- 2020/09/12 06:01 [medline] PHST- 2020/08/15 00:00 [pmc-release] AID - S2214-7500(20)30370-X [pii] AID - 10.1016/j.toxrep.2020.08.008 [doi] PST - epublish SO - Toxicol Rep. 2020 Aug 15;7:1032-1038. doi: 10.1016/j.toxrep.2020.08.008. eCollection 2020.