D-Penicillamine prolongs survival and lessens copper-induced toxicity in Drosophila melanogaster

被引:14
作者
Abolaji, Amos Olalekan [1 ]
Fasae, Kehinde Damilare [1 ]
Iwezor, Chizim Elizabeth [1 ]
Farombi, Ebenezer Olatunde [1 ]
机构
[1] Univ Ibadan, Coll Med, Fac Basic Med Sci, Dept Biochem,Drosophila Lab,Mol Drug Metab & Toxi, Ibadan, Nigeria
关键词
Copper; Oxidative stress; D-Penicillamine; Drosophila melanogaster; ALZHEIMERS-DISEASE; OXIDATIVE STRESS; CEREBROSPINAL-FLUID; PARKINSONS-DISEASE; WILSONS-DISEASE; IRON; ACETYLCHOLINESTERASE; TRANSPORT; MECHANISM; EXPOSURE;
D O I
10.1093/toxres/tfaa032
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 [卫生毒理学];
摘要
D-penicillamine (DPA) is an amino-thiol that has been established as a copper chelating agent for the treatment of Wilson's disease. DPA reacts with metals to form complexes and/or chelates. Here, we investigated the survival rate extension capacity and modulatory role of DPA on Cu2+-induced toxicity in Drosophila melanogaster. Adult Wild type (Harwich strain) flies were exposed to Cu2+ (1 mM) and/or DPA (50 mu M) in the diet for 7 days. Additionally, flies were exposed to acute Cu2+ (10 mM) for 24 h, followed by DPA (50 mu M) treatment for 4 days. Thereafter, the antioxidant status [total thiol (T-SH) and glutathione (GSH) levels and glutathione S-transferase and catalase activities] as well as hydrogen peroxide (H2O2) level and acetylcholinesterase activity were evaluated. The results showed that DPA treatment prolongs the survival rate of D. melanogaster by protecting against Cu2+-induced lethality. Further, DPA restored Cu2+-induced depletion of T-SH level compared to the control (P < 0.05). DPA also protected against Cu2+ (1 mM)-induced inhibition of catalase activity. In addition, DPA ameliorated Cu2+-induced elevation of acetylcholinesterase activity in the f lies. The study may therefore have health implications in neurodegenerative diseases involving oxidative stress such as Alzheimer's disease.
引用
收藏
页码:346 / 352
页数:7
相关论文
共 68 条
[1]
Curcumin attenuates copper-induced oxidative stress and neurotoxicity in Drosophila melanogaster [J].
Abolaji, Amos O. ;
Fasae, Kehinde D. ;
Iwezor, Chizim E. ;
Aschner, Michael ;
Farombi, Ebenezer O. .
TOXICOLOGY REPORTS, 2020, 7 :261-268
[2]
Adie, 2018, BIOCHEM BIOPH RES CO, P1
[3]
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[4]
Manganese transport in eukaryotes: The role of DMT1 [J].
Au, Catherine ;
Benedetto, Alexandre ;
Aschner, Michael .
NEUROTOXICOLOGY, 2008, 29 (04) :569-576
[5]
A Drosophila model of Menkes disease reveals a role for DmATP7 in copper absorption and neurodevelopment [J].
Bahadorani, Sepehr ;
Bahadorani, Peyman ;
Marcon, Edyta ;
Walker, David W. ;
Hilliker, Arthur J. .
DISEASE MODELS & MECHANISMS, 2010, 3 (1-2) :84-91
[6]
Copper homeostasis in Drosophila by complex interplay of import, storage and behavioral avoidance [J].
Balamurugan, Kuppusamy ;
Egli, Dieter ;
Hua, Haiqing ;
Rajaram, Rama ;
Seisenbacher, Gerhard ;
Georgiev, Oleg ;
Schaffner, Walter .
EMBO JOURNAL, 2007, 26 (04) :1035-1044
[7]
Neurodegenerative diseases and oxidative stress [J].
Barnham, KJ ;
Masters, CL ;
Bush, AI .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (03) :205-214
[8]
Acute and chronic metal exposure impairs locomotion activity in Drosophila melanogaster: a model to study Parkinsonism [J].
Bonilla-Ramirez, Leonardo ;
Jimenez-Del-Rio, Marlene ;
Velez-Pardo, Carlos .
BIOMETALS, 2011, 24 (06) :1045-1057
[10]
Expression and localisation of the essential copper transporter DmATP7 in Drosophila neuronal and intestinal tissues [J].
Burke, Richard ;
Commons, Elizabeth ;
Camakaris, James .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2008, 40 (09) :1850-1860