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1.
Neurotox Res ; 39(4): 1103-1115, 2021 Aug.
Article in English | MEDLINE | ID: mdl-33689146

ABSTRACT

Although many studies have reported toxic effects of cadmium (Cd) and lead (Pb) in the central nervous system, few studies have investigated the combined toxicity of Cd and Pb. The mechanisms by which these combined heavy metals induce toxicity, as well as effective means to exert neuroprotection from these agents, remain poorly understood. To investigate the protective effects of alpha-lipoic acid (α-LA) on Cd- and/or Pb-induced cortical damage in rats, 48 Sprague-Dawley rats were exposed to drinking water containing 50 mg/L of Cd and/or 300 mg/L of Pb for 12 weeks, in the presence or absence of α-LA co-treatment (50 mg/kg) via gavage. We observed that exposure to Cd and/or Pb decreased the brain weight/body weight ratio and increased Cd and/or Pb contents as well as ultrastructural damage to the cerebral cortex. Cd and/or Pb also induced endoplasmic-reticulum (ER) stress and activated Fas (CD95/APO-1)/Fas ligand (FasL) and mitochondrial apoptotic pathways. Furthermore, co-treatment of Cd and Pb further exacerbated part of these phenotypes than treatment of Cd or Pb alone. However, simultaneous supplementation with α-LA attenuated Cd and/or Pb-induced neurotoxicity by increasing the brain weight/body weight ratio, reducing Cd and/or Pb contents, ameliorating both nuclear/mitochondrial damage and ER stress, and attenuating activation of Fas/FasL and mitochondrial apoptotic pathways. Collectively, our results indicate that the accumulation of Cd and/or Pb causes cortical damage and that α-LA exerts protection against Cd- and/or Pb-induced neurotoxicity. These findings highlight that α-LA may be exploited for the treatment and prevention of Cd- and/or Pb-induced neurotoxicity.


Subject(s)
Cadmium/toxicity , Cerebral Cortex/drug effects , Endoplasmic Reticulum Stress/drug effects , Fas Ligand Protein/antagonists & inhibitors , Lead/toxicity , Thioctic Acid/pharmacology , fas Receptor/antagonists & inhibitors , Animals , Antioxidants/pharmacology , Apoptosis/drug effects , Apoptosis/physiology , Cerebral Cortex/metabolism , Cerebral Cortex/ultrastructure , Endoplasmic Reticulum Stress/physiology , Fas Ligand Protein/metabolism , Female , Mitochondria/drug effects , Mitochondria/metabolism , Mitochondria/ultrastructure , Rats , Rats, Sprague-Dawley , fas Receptor/metabolism
2.
Vet J ; 181(3): 321-5, 2009 Sep.
Article in English | MEDLINE | ID: mdl-18682334

ABSTRACT

The aim of this study was to determine whether receptor activator of nuclear factor NF-kappaB ligand (RANKL), osteoprotegerin (OPG) and a calcium:phosphorus (Ca:P) ratio of 2:1 could affect survival and activation of Muscovy duck osteoclasts (OCs). Bone marrow cells were obtained from 5-day-old Muscovy ducks and cultured with (Group A) No added factors, (B) 30ng/mL soluble RANKL (sRANKL), (C) 30ng/mL sRANKL and 10ng/mL OPG, (D) 10ng/mL OPG, (E) 50ng/mL OPG, (F) 100ng/mL OPG and (G) 30ng/mL sRANKL, 6mmol/L Ca and 3mmol/L P. sRANKL promoted the survival of OCs on day 2, whereas the number of OCs decreased with addition of OPG in a dose-dependent manner. OPG and Ca:P (2:1) both inhibited OC survival induced by RANKL. RANKL stimulated bone resorption by OCs, whereas OPG, but not Ca:P (2:1), inhibited the activity of OCs induced by RANKL. RANKL promotes the survival and activation of OCs from Muscovy ducks, whereas OPG and, to a lesser extent, Ca:P (2:1) reduce the life span and inhibited the activation of OCs induced by RANKL.


Subject(s)
Calcium/pharmacology , Ducks , Osteoclasts/cytology , Osteoclasts/drug effects , Osteoprotegerin/pharmacology , Phosphorus/pharmacology , RANK Ligand/pharmacology , Animals , Cells, Cultured
3.
Zhongguo Zhong Yao Za Zhi ; 33(10): 1161-3, 2008 May.
Article in Chinese | MEDLINE | ID: mdl-18720867

ABSTRACT

The difference of ingredients between the roots from the SP1 plants of Achyranthes Bidentata carried by satellite and the control's were evaluated in this study. The techniques of ultraviolet-visible spectroscopy (UVS), infrared spectroscopy (IR), Xray diffraction (XRD) and SDS-PAGE were used to analyse the chemical constituent in the root of A. bidentata. The results demonstrated that the UVS, IR, XRD and protein fingerprints of the roots from A. bidentata were distinct with special characters. The difference of the IR, XRD and protein fingerprints could be discriminated the satellite plants roots from those of the control, however, there were no difference of the UVS fingerprints between the satellite plants roots and the control. This indicated that the kinds of chemical ingredients were not different between the two groups, but the contents of some chemical ingredients deceased in SP1 plants of A. bidentata carried by satellite.


Subject(s)
Achyranthes/chemistry , Drugs, Chinese Herbal/chemistry , Space Flight , Plant Roots/chemistry , Resins, Plant/chemistry
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