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5 protocols using ng nitro l arginine l nna

1

Studying Vascular Endothelial Function

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Phenylephrine,9 (link) ACh,9 (link) RN1734,7 (link) GSK1016790A,13 (link) NG-nitro-L-arginine (L-NNA),8 (link) indomethacin,8 (link) and apamin8 (link) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Anti-KCa2.3 (catalog No. APC-025) and anti-TRPV4 (catalog No. ACC-034) antibodies were purchased from Alomone Labs.
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2

Pharmacological Effects of Vasoactive Agents

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The following drugs were used: atropine sulphate and granisetron hydrochloride dissolved in saline (Sigma Chemical Co., St. Louis, Missouri, United States). Zinc protoporphyrin IX and hemin were dissolved in 0.1 N NaOH and equilibrated to a pH of 7.4 with HCl (Sigma Chemical Co., St. Louis, Missouri, United States). Tricarbonyl Chloro(glycinato)ruthenium (II) (CORM-3) and NG-nitro-L-Arginine (L-NNA) were dissolved in distilled water (Sigma Chemical Co., St. Louis, Missouri, United States). In in vivo studies, vehicle-treated rats received the same amount of vehicle as did drug-treated animals. In in vitro experiments, vehicle-treated preparations were exposed to the same amount of vehicle as drug-treated preparations.
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3

Vasodilator Evaluation in Murine Preparations

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AF B1, a nitric oxide (NO) synthase inhibitor [NG-nitro-L-arginine (L-NNA)], and atropine sulfate were obtained from Sigma-Aldrich (Merck KGaA). A 2 mg/ml stock solution of AF was prepared in dimethyl sulfoxide (which does not directly affect murine-isolated smooth muscle preparations) and stored at 0–4°C. Other drugs were dissolved in ethanol and deionized water (1:1) as 1 mg/ml stock solutions, and were subsequently diluted in deionized water before use.
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4

Pharmacological Modulation of Signaling Pathways

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Acetylcholine (ACh), carbamoylcholine chloride (carbachol), Bay K8644, trifluoperazine dihydrochloride, apamin, charybdotoxin (ChTX), glibenclamide, quinine, verapamil, papaverine dihydrochloride, H-89 dihydrochloride hydrate, KT-5823, chelerythrine chloride, (+)-(R)-trans-4-(1-aminoethyl)-N-(4-pyridyl) cyclohexanecarboxamide dihydrochloride monohydrate (Y-27632), dibutyryl-cAMP (d-cAMP), d,l-propargylglycine (PAG), aminooxyacetic acid hemihydrochloride (AOAA), tetrodotoxin (TTX) and NG-nitro-l arginine (l-NNA) were obtained from Sigma (Madrid, Spain). Tram-34, 1H-[1,2,4]oxadiazolo [4,3-α]quinoxalin-1-one (ODQ), Rp-8-Br-PET-cGMPS, okadaic acid and forskolin were purchased from Tocris (Madrid, Spain). All chemicals were of analytical grade. Bay K8644 was dissolved in ethanol. apamin was diluted in acetic acid. glibenclamide, Tram-34, forskolin (Fk), okadaic acid and ODQ were prepared in dimethyl sulfoxide. All other chemicals were dissolved in distilled water.
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5

Pharmacological Modulation of Cerebellar Signaling

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The reagents included picrotoxin, D-(-)-2-amino-5-phosphonopentanoic acid (D-APV), NG-Nitro-L-arginine (L-NNA), nitric oxide synthase (NOS) inhibitor, nicotine, methyllycaconitine citrate hydrate (MLA), and dihydro-β-erythroidine hydrobromide (DβEH) bought from Sigma-Aldrich (Shanghai, China). All these chemicals were dissolved in solution and kept in frozen aliquots. For experiments with NOS inhibitor, L-NNA, cerebellar surface was superfused with 200 μM L-NNA for 1 h before recordings were began. The drugs were dissolved in ACSF and applied directly onto the cerebellar surface by a peristaltic pump (0.5 ml/min).
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