الصفحة الرئيسية>>Signaling Pathways>> Ubiquitination/ Proteasome>> Mitophagy>>6-Hydroxydopamine hydrobromide

6-Hydroxydopamine hydrobromide (Synonyms: 6-hydroxy Dopamine, Oxidopamine, 2,4,5-Trihydroxyphenethylamine)

رقم الكتالوجGC16267

أوكسيدوبامين (6-OHDA) هي مضاد للمحول العصبي دوبامين.

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6-Hydroxydopamine hydrobromide التركيب الكيميائي

Cas No.: 636-00-0

الحجم السعر المخزون الكميّة
50mg
36٫00
متوفر

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Sample solution is provided at 25 µL, 10mM.

Product has been cited by 2 publications

Description of 6-Hydroxydopamine hydrobromide

6-Hydroxydopamine hydrobromide (6-OHDA) is a structural analogue of catecholamines, dopamine and noradrenaline, and exerts its toxic effects on catecholaminergic neurons. The neurotoxin 6-hydroxydopamine continues to constitute a valuable topical tool used chiefly in modeling Parkinson's disease (PD) in the rat [1].

The classical method of intracerebral infusion of 6-Hydroxydopamine hydrobromide, involving a massive destruction of nigrostriatal dopaminergic neurons, is largely used to investigate motor and biochemical dysfunctions in Parkinson's disease [1]

6-Hydroxydopamine hydrobromide undergoes robust auto-oxidation generating cytotoxic H2O2, reactive oxygen species (ROS) and catecholamine quinones which attack endocellular nucleophilic groups [2].

Neurotoxic effects of 6-Hydroxydopamine hydrobromide occur through a two-step mechanism involving accumulation of the toxin into catecholaminergic neurons, followed by alteration of cellular homeostasis and neuronal damage. Intracellular storage of 6-Hydroxydopamine hydrobromide is mediated by the dopamine or noradrenaline membrane transporters (DAT and NAT respectively), which recognize and uptake 6-Hydroxydopamine hydrobromide due to its structural similarity with endogenous catecholamines [3]. 6-Hydroxydopamine hydrobromide is infused unilaterally in the MFB, producing a functional imbalance between the dopaminergic nigrostriatal systems and resulting in motor slowness, indicative of parkinsonian-like akinesia, and typical rotational behaviour in response to dopaminomimetic agents [4].

References:
[1]. Simola N, Morelli M, Carta A R. The 6-hydroxydopamine model of Parkinson's disease[J]. Neurotoxicity research, 2007, 11(3): 151-167.
[2]. Palumbo A, A Napolitano, P Barone and M d'Ischia (1999) Nitrite- and peroxide-dependent oxidation pathways of dopamine: 6-nitrodopamine and 6-hydroxydopamine formation as potential contributory mechanisms of oxidative stress- and nitric oxide-induced neurotoxicity in neuronal degeneration. Chem. Res. Toxicol. 12, 1213-1222.
[3]. Luthman J, A Fredriksson, E Sundstrom, G Jonsson and T.Archer (1989) Selective lesion of central dopamine or noradrenaline neuron systems in the neonatal rat: motor behavior and monoamine alterations at adult stage. Behav. Brain.Res. 33, 267-277.
[4]. Ungerstedt U and G Arbuthnott (1970) Quantitative recording of rotational behavior in rats after 6-hydroxydopamine lesions of the nigrostriatal dopamine system. Brain Res. 24, 485-493.

Protocol of 6-Hydroxydopamine hydrobromide

Cell experiment [1]:

Cell lines

Primary nigral cells (PNCs)

Preparation Method

The conditioned media were replaced with new media containing AS-IV at the final concentration indicated with or without 200 µM of 6-Hydroxydopamine hydrobromide.

Reaction Conditions

200µM for 24 hours

Applications

Compared with vehicle controls, exposure to 200 µM 6-Hydroxydopamine resulted in the loss of 75% of PNCs, as determined using the LDH assay.

Animal experiment [2]:

Animal models

Female Sprague-Dawley rats

Preparation Method

The animals received a single, intrastriatal injection of 6-Hydroxydopamine hydrobromide. Twenty-five micrograms of 6-Hydroxydopamine hydrobromide, which was dissolved in 1.5 µl of normal saline with 0.2% ascorbic acid, was injected at a depth of 5.6 mm ventral to the skull at the same anterior/posterior and medial/lateral coordinates at which the cells had been injected. The injection site was chosen to be midway between the two implant sites. 6-Hydroxydopamine hydrobromide was injected over 5 min, and the needle was left in place for an additional 5 min before withdrawal of the needle.

Dosage form

25 µg in 1.5 µl of normal saline with 0.2% ascorbic acid

Applications

Induced neurodegeneration in the SNc by unilateral injection of 6-hydroxydopamine hydrobromide into mfb, act as 6-OHDA lesion model

References:
[1]: Chan W S, Durairajan S S K, Lu J H, et al. Neuroprotective effects of Astragaloside IV in 6-hydroxydopamine-treated primary nigral cell culture[J]. Neurochemistry International, 2009, 55(6): 414-422.
[2]: Shults C W, Ray J, Tsuboi K, et al. Fibroblast growth factor-2-producing fibroblasts protect the nigrostriatal dopaminergic system from 6-hydroxydopamine[J]. Brain research, 2000, 883(2): 192-204.

Chemical Properties of 6-Hydroxydopamine hydrobromide

Cas No. 636-00-0 SDF
المرادفات 6-hydroxy Dopamine, Oxidopamine, 2,4,5-Trihydroxyphenethylamine
Chemical Name 5-(2-aminoethyl)benzene-1,2,4-triol hydrobromide
Canonical SMILES OC(C(CCN)=C1)=CC(O)=C1O.Br
Formula C8H11NO3.HBr M.Wt 250.09
الذوبان ≥ 25mg/mL in DMSO with ultrasonic Storage Store at 4°C,stored under nitrogen,unstable in solution, ready to use.
General tips Please select the appropriate solvent to prepare the stock solution according to the solubility of the product in different solvents; once the solution is prepared, please store it in separate packages to avoid product failure caused by repeated freezing and thawing.Storage method and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored at -20°C, please use it within 1 month.
To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time.
Shipping Condition Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request.

Complete Stock Solution Preparation Table of 6-Hydroxydopamine hydrobromide

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1 mg 5 mg 10 mg
1 mM 3.9986 mL 19.9928 mL 39.9856 mL
5 mM 0.7997 mL 3.9986 mL 7.9971 mL
10 mM 0.3999 mL 1.9993 mL 3.9986 mL
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Average Rating: 5 ★★★★★ (Based on Reviews and 38 reference(s) in Google Scholar.)

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