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6 ohda hydrochloride

Manufactured by Bio-Techne
Sourced in United Kingdom

6-OHDA hydrochloride is a neurotoxin commonly used in research applications. It is a white crystalline powder that is soluble in water and other polar solvents. The core function of 6-OHDA hydrochloride is to induce selective degeneration of catecholaminergic neurons in experimental models.

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2 protocols using 6 ohda hydrochloride

1

Unilateral 6-OHDA Lesion in Rats

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The experimental design was performed according to a previously described procedure (25 (link)). Twenty minutes before surgery, rats were injected intra-peritoneally with pargyline (50 mg/kg, Sigma, Saint-Quentin Fallavier, France). Rats were anesthetized with isoflurane (4%, 500 mL/min) and placed on a stereotaxic apparatus (Stoelting, Phymep, Paris, France) and maintained under isoflurane 2.5% (500 mL/min) during surgery. The skull was exposed and small holes were made with a dental drill. Lesion was carried out by unilateral intrastriatal injection of 6-OHDA hydrochloride (1 mg/mL, Tocris Bioscience, Bristol, UK). A total of 10 μg of 6-OHDA was administered in two areas of the right striatum (1 mg/mL in 0.01% ascorbic acid, pH 4.5, i.e., 5 μg in 5 μL for each area) with a Hamilton syringe (gage 25, Hamilton, Massy, France) at a flow rate of 1 μL/min. Coordinates from bregma were AP = +0.5 mm, L = −2.5 mm, P = −5 mm, and AP = −0.5 mm, L = −4 mm, P = −5 mm according to Paxinos and Watson atlas (26 ). The needle was left in place for 4 min after injection and then removed slowly to optimize toxin diffusion. After surgery, the rats were given buprenorphine (0.05 mg/kg sub-cutaneously) for postoperative pain and were allowed to recover from surgery for 7 days before being subjected to the imaging experiments.
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2

Targeted Dopaminergic Depletion in Bird

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Adult male birds received bilateral injections of either 400nl 6-OHDA solution into HVC or 80–100nl 6-OHDA solution into A11 (N=4 for A11 and N=5 HVC). The solution was PBS-based and included 10–60 mM 6-OHDA hydrochloride (Tocris, 2547), 10 μM l-ascorbic acid (Millipore/Sigma, A92902), and 1 μM desipramine hydrochloride (Tocris, 3067), which was included as an inhibitor for noradrenaline and serotonin transporters to protect noradrenergic and serotonergic neuron terminals at the injection site. Control birds received an injection of PBS with 10 μM ascorbic acid and 1 μM desipramine (N=6 for A11 sham group and N=5 for HVC sham group). Drugs were dissolved in PBS immediately before injection in place of equimolar NaCl (working solution: ~300 mOsm, pH 7.3). After injection, birds were returned to their original home cage until approximately 14 days post injection.
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