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Sodium cyanide nacn

Manufactured by Merck Group
Sourced in Australia, United States

Sodium cyanide (NaCN) is an inorganic compound that consists of a sodium cation (Na+) and a cyanide anion (CN−). It is a white, crystalline solid that is highly soluble in water. Sodium cyanide is commonly used as a precursor in the production of other chemicals and in various industrial processes.

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4 protocols using sodium cyanide nacn

1

Chemoreflex Response to Sodium Cyanide

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Sodium cyanide (NaCN; 50–100 µL; 0.4 µg/µL, Sigma-Aldrich, Australia) was injected as a bolus directly into the aorta from a pre-calibrated 100 µL Hamilton syringe to stimulate the CB chemoreceptors. The chemoreflex consisted of increased PN activity, bradycardia, sympathoexcitation, and an increase in PP. We quantified the chemoreflex in two ways: first, calculating the percentage increase in respiratory rate (i.e. tachypnoea) and sympathoexcitation relative to the baseline immediately before the stimulus; the period of baseline used for this calculation was of the same time-length as the chemoreflex response (e.g. 7 s). Second, the maximum bradycardia and increase in PP were calculated as the change (Δ) in HR (bpm) and PP (mmHg) relative to the baseline. Two consecutive chemoreflex responses of the same magnitude were obtained before initiating subsequent protocols (see below). At least 7 min were allowed to elapse between each NaCN dose.
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2

Amino Acid Quantification Protocol

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Arginine (Arg), aspartate (Asp), citrulline (Cit), glutamate (Glu), histamine (Hist), and taurine (Tau) were obtained from Sigma Aldrich (St Louis, MO). Standards of each amine were prepared at 2 mM concentrations in 18.2 MΩ /cm deionized water (Millipore, Billerica, MA). Subsequent dilutions of each stock solution were made prior to analysis. Naphthalene-2,3-dicarboxaldehyde (NDA) (Invitrogen, Carlsbad, CA) was prepared in acetonitrile (Fisher Scientific, Pittsburgh, PA) to a concentration of 5 mM. Sodium cyanide (NaCN) (Sigma Aldrich) was dissolved in water to a final concentration of 10 mM. Stock solutions of both NDA and NaCN were made weekly and stored at 4°C, protected from light exposure. Stock solutions of sulfobutylether-β-cyclodextrin (SBEC) (Life Technologies, Grand Island NY) were made on a weekly basis to a concentration of 10 mM in deionized water and stored at 4°C. Finally, the background electrolyte (BGE) consisted of 1.4 mM SBEC, 10% by volume HPLC-grade dimethylsulfoxide (Fisher Scientific), and sodium tetraborate (Sigma Aldrich) at a final concentration of 15 mM. Finally, the pH of the BGE was measured using a pH meter and adjusted to 9.2 with 1 M sodium hydroxide (Fisher Scientific).
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3

Murine RAW 264.7 Cell Culture Protocol

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Murine RAW 264.7 cells (ATCC® TIB71), Dulbecco’s Modified Eagle’s Medium (DMEM), phenol red-free DMEM, fetal bovine serum (FBS), and penicillin/streptomycin antibiotic solution were purchased from American Type Culture Collection (ATCC, Manassas, VA, USA). L-carnosine, sodium cyanide (NaCN), anhydrous dimethyl sulfoxide (DMSO), phosphate-buffered saline (PBS), Trypan blue solution, lipopolysaccharides (LPS), Triton X-100, and bovine serum albumin (BSA) were all supplied by Sigma-Aldrich (St. Louis, MO, USA). Sodium hydroxide (NaOH), hydrochloric acid (HCl), 25 mL polystyrene culture flasks, boric acid, and ethanol (95%) were obtained from Fisher Scientific (Pittsburgh, PA, USA). Interferon-γ (IFN-γ) was supplied by Calbiochem (Gibbstown, NJ, USA). Naphthalene-2,3-dicarboxaldehyde (NDA) was obtained from Invitrogen (Carlsbad, CA, USA). Polyethersulfone (PES) membrane (3K) was purchased from VWR International (West Chester, PA, USA). C-Chip disposable hemocytometer was purchased from Bulldog Bio, Inc. (Portsmouth, NH, USA). All water used was Ultrapure (18.3 MΩ cm) (Milli-Q Synthesis A10, Millipore, Burlington, MA, USA).
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4

Cell Imaging with Pharmacological Modulators

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Most of the techniques used in this study have been described in detail elsewhere [7 (link)]. The bath solution for cell imaging consisted of (in mM) 140 NaCl, 5 KCl, 1.1 MgCl2, 2.5 CaCl2, 10 HEPES, with the pH adjusted to 7.2 with NaOH. N-methyl-d-glucamine was added to maintain the solutions’ osmolarity. Five mM glucose was always added to the bath solutions (with or without HK expression), so that HK would be active when present. Solutions were perfused directly over the cells using a gravity-fed eight-way perfusion device (Warner Instruments, Hamden, CT, USA) with electrically controlled solenoids (The Lee Company, Westbrook, CT, USA). Input and output of solution to the recording chamber (glass bottomed Petri dish) were equilibrated to maintain constant flow rates and volumes. Sodium Cyanide (NaCN) and 6-Aminonicotinamide (6-AN) were purchased from Sigma-Aldrich. The inhibitor of ME1 (ME1*) was purchased from (ProbeChem Biochemicals, Shanghai, China).
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