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Comparative Study
. 2009 Mar;30(2):240-8.
doi: 10.1016/j.neuro.2008.12.007. Epub 2008 Dec 25.

Chelation therapy of manganese intoxication with para-aminosalicylic acid (PAS) in Sprague-Dawley rats

Affiliations
Comparative Study

Chelation therapy of manganese intoxication with para-aminosalicylic acid (PAS) in Sprague-Dawley rats

Wei Zheng et al. Neurotoxicology. 2009 Mar.

Abstract

Para-aminosalicylic acid (PAS), an FDA-approved anti-tuberculosis drug, has been used successfully in the treatment of severe manganese (Mn)-induced Parkinsonism in humans [Jiang Y-M, Mo X-A, Du FQ, Fu X, Zhu X-Y, Gao H-Y, et al. Effective treatment of manganese-induced occupational Parkinsonism with p-aminosalicylic acid: a case of 17-year follow-up study. J Occup Environ Med 2006;48:644-9]. This study was conducted to explore the capability of PAS in reducing Mn concentrations in body fluids and tissues of Mn-exposed animals. Sprague-Dawley rats received daily intraperitoneally (i.p.) injections of 6mg Mn/kg, 5 days/week for 4 weeks, followed by a daily subcutaneously (s.c.) dose of PAS (100 and 200mg/kg as the PAS-L and PAS-H group, respectively) for another 2, 3 or 6 weeks. Mn exposure significantly increased the concentrations of Mn in plasma, red blood cells (RBC), cerebrospinal fluid (CSF), brain and soft tissues. Following PAS-H treatment for 3 weeks, Mn levels in liver, heart, spleen and pancreas were significantly reduced by 25-33%, while 3 weeks of PAS-L treatment did not show any effect. Further therapy with PAS-H for 6 weeks reduced Mn levels in striatum, thalamus, choroid plexus, hippocampus and frontal cortex by 16-29% (p<0.05). Mn exposure greatly increased iron (Fe) and copper (Cu) concentrations in CSF, brain and liver. Treatment with PAS-H restored Fe and Cu levels comparable with control. These data suggest that PAS likely acts as a chelating agent to mobilize and remove tissue Mn. A high-dose and prolonged PAS treatment appears necessary for its therapeutic effectiveness.

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Figures

Figure 1
Figure 1
% Reduction of Mn concentrations in selected brain regions and RBC following PAS chelation therapy. Sprague-Dawley rats in the Mn-alone group received ip. injections of 6 mg Mn/kg, 5 days/week for 4 weeks, followed by sc. saline for 2, 3, or 6 weeks. Rats in the Mn-PAS groups received ip. injections of 6 mg Mn/kg, 5 days/week for 4 weeks, followed by sc. injections of 200 mg PAS/kg for 2, 3, or 6 weeks. Mn concentrations were determined by AAS (n=5–8 in each group). The values in the Mn-PAS group were compared with those in the Mn-alone group and expressed as % of reduction.
Figure 2
Figure 2
Changes of Mn concentrations in major organs of animals exposed to Mn and treated with PAS. Rats in the control group received daily ip. saline injections throughout the entire experiment. Animals in the Mn-alone group received ip. injections of 6 mg Mn/kg, 5 days/week for 4 weeks, followed by sc. saline for 2, 3, or 6 weeks. Rats in the Mn-PAS groups received ip. injections of 6 mg Mn/kg, 5 days/week for 4 weeks, followed by sc. injection of 200 mg PAS/kg for another 2, 3, or 6 weeks. Data represent mean ± SD, n=6–8.*: p<0.05,**: p<0.01 as compared to the saline group; #: p<0.05, ##: p<0.01 as compared to the Mn-alone group.

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References

    1. Aschner M, Aschner JL. Manganese transport across the blood–brain barrier: relationship to iron homeostasis. Brain Res Bull. 1990;24:857–860. - PubMed
    1. Aschner M, Nass R, Guilarte TR, Schneider JS, Zheng W. Manganese: Recent advances in understanding its transport and neurotoxicity. Toxicol Appl Pharmacol. 2007;221:131–147. - PMC - PubMed
    1. Bowler RM, Gysens S, Diamond E, Nakagawa S, Drezgic M, Roels HA. Manganese exposure: Neuropsychological and neurological symptoms and effects in welders. Neurotoxicology. 2006;27:315–326. - PubMed
    1. Calne DB, Chu NS, Huang CC, Lu CS, Olanow W. Manganism and idiopathic parkinsonism: similarities and differences. Neurology. 1994;44:1583–1586. - PubMed
    1. Chandra SV, Shukla GS, Srivastawa RS, Singh H, Gupta VP. An exploratory study of manganese exposure to welders. Clin Toxicol. 1981;18:407–416. - PubMed

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