کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4318844 1613255 2014 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Contaminating levels of zinc found in commonly-used labware and buffers affect glycine receptor currents
ترجمه فارسی عنوان
سطوح آلاینده روی موجود در آزمایشگاه ها و بافر های معمول استفاده می شود که جریان های گیرنده گلیسین را تحت تاثیر قرار می دهند
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب سلولی و مولکولی
چکیده انگلیسی


• Zinc is a contaminant in common electrophysiological buffers and labware.
• Contaminating zinc levels enhance glycine receptor function.
• Different vial types do not affect zinc mediated glycine receptor enhancement.
• Washing vials did not affect zinc mediated glycine receptor enhancement.
• Use of polystyrene serological pipets can lead to zinc contamination of solutions.

Zinc is an allosteric modulator of glycine receptor function, enhancing the effects of glycine at nM to low μM concentrations, and inhibiting its effects at higher concentrations. Because of zinc's high potency at the glycine receptor, there exists a possibility that effects attributed solely to exogenously-applied glycine in fact contain an undetected contribution of zinc acting as an allosteric modulator. We found that glycine solutions made up in standard buffers and using deionized distilled water produced effects that could be decreased by the zinc chelator tricine. This phenomenon was observed in three different vials tested and persisted even if vials were extensively washed, suggesting the zinc was probably present in the buffer constituents. In addition, polystyrene, but not glass, pipets bore a contaminant that enhanced glycine receptor function and that could also be antagonized by tricine. Our findings suggest that without checking for this effect using a chelator such as tricine, one cannot assume that responses elicited by glycine applied alone are not necessarily also partially due to some level of allosteric modulation by zinc.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Brain Research Bulletin - Volume 100, January 2014, Pages 1–5
نویسندگان
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