posted on 2016-11-07, 15:53authored byR. J. Smeyne, C. B. Breckenridge, M. Beck, Y. Jiao, M. T. Butt, J. C. Wolf, D. Zadory, D. J. Minnema, N. C. Sturgess, K. Z. Travis, A. R. Cook, Lewis L. Smith, P. A. Botham
The neurotoxicity of paraquat dichloride (PQ) was assessed in two inbred strains of 9- or 16-week old male C57BL/6 mice housed in two different laboratories and compared to the effects of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). PQ was administered by intraperitoneal injections; either once (20 mg/kg) or twice (10 mg/kg) weekly for 3 weeks, while MPTP-HCl was injected 4 times on a single day (20 mg/kg/dose). Brains were collected 8, 16, 24, 48, 96 or 168 hours after the last PQ treatment, and 48 or 168 hours after MPTP treatment. Dopamine neurons in the substantia nigra pars compacta (SNpc) were identified by antibodies to tyrosine hydroxylase (TH+) and microglia were identified using Iba-1 immunoreactivity. The total number of TH+ neurons and the number of resting and activated microglia in the SNpc at 168 hours after the last dose were estimated using model- or design-based stereology, with investigators blinded to treatment. In a further analysis, a pathologist, also blinded to treatment, evaluated the SNpc and/or striatum for loss of TH+ neurons (SNpc) or terminals (striatum), cell death (as indicated by amino cupric silver uptake, TUNEL and/or caspase 3 staining) and neuroinflammation (as indicated by Iba-1 and/or GFAP staining). PQ, administered either once or twice weekly to 9- or 16-week old mice from two suppliers, had no effect on the number of TH+ neurons or microglia in the SNpc, as assessed by two groups, each blinded to treatment, using different stereological methods. PQ did not induce neuronal cell loss or degeneration in the SNpc or striatum. Additionally, there was no evidence of apoptosis, microgliosis or astrogliosis. In MPTP-treated mice, the number of TH+ neurons in the SNpc was significantly decreased and the number of activated microglia increased. Histopathological assessment found degenerating neurons/terminals in the SNpc and striatum but no evidence of apoptotic cell death. MPTP activated microglia in the SNpc and increased the number of astrocytes in the SNpc and striatum.
Funding
Funding: This work was funded by Syngenta Crop
Protection LLC (CBB, MTB, MB, JCW, DZ, DJM,
NCS, KZT, ARC, LLS and PAB) and ALSAC (RJS
and YJ). The funder provided support in the form
of salaries for authors CBB and DJM. Syngenta
Limited provided support in the form of salaries for
authors NCS, KZT, ARC and PAB. Support for
authors in the form of salaries was provided by WIL Research Laboratories LLC (MB), Tox Path
Specialists LLC (MTB) and Experimental Pathology
Laboratories Inc (JCW & DZ). LLS received
support in the form of consultancy fees provided
by Syngenta Limited. RJS and YJ conducted
studies and evaluations at SJCRH under contract to
Syngenta Crop Protection LLC. The specific roles
of these authors are articulated in the ‘author
contributions’ section.
History
Citation
PLoS One, 2016, 11(10): e0164094
Author affiliation
/Organisation/COLLEGE OF MEDICINE, BIOLOGICAL SCIENCES AND PSYCHOLOGY