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Reserpine

Manufactured by Nacalai Tesque
Sourced in Japan

Reserpine is a laboratory reagent used in the study of various biological and biochemical processes. It is a phytochemical compound derived from the roots of the Rauwolfia serpentina plant. Reserpine is commonly used as a research tool to investigate the mechanisms of action and effects of certain drugs and neurotransmitters.

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5 protocols using reserpine

1

Reserpine-Induced Animal Model of Fibromyalgia

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An animal model of FM was produced using the protocol described in previous studies (31 (link), 34 (link), 35 (link)). Reserpine (Nacalai Tesque, Inc., Kyoto, Japan), adjusted to a concentration of 0.25 mg/mL with 0.5% acetic acid, was injected (0.25 mg/kg, s.c.) into the back skin once a day for 3 successive days (RES group). As a control, a vehicle solution (0.5% acetic acid) was similarly injected (VEH group).
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2

Reserpine-Induced Fibromyalgia in Mice

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To induce FM in the model mice, Reserpine was injected through the intraperitoneal route (1 mL/kg) into wild-type mice once a day for 3 days (Nagakura et al., 2009 (link)). Reserpine, purchased from Nacalai Tesque (product No.: 30013-81, Kyoto, Japan), was dissolved in 100% glacial acetic acid (1 mg/0.05 mL) (solution A). Subsequently, distilled water (1 mg/0.95 mL) was added to solution A (solution B, 1 mg/1 mL), containing 5% glacial acetic acid to create solution B. Following this, solution B was diluted to a final concentration of 0.5% acetic acid with distilled water (stock solution), which was subcutaneously injected into the mice 3 times, at a dosage of 1 mL/kg.
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3

Reserpine-Induced Fibromyalgia Model in Mice

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To induce FM in the mice, an intraperitoneal Reserpine injection (1 mL/kg) was administered to wild-type mice once a day for three days [25 (link)]. Reserpine was purchased from Nacalai Tesque (No. 30013–81, Kyoto, Japan) and dissolved in 100% glacial acetic acid (1 mg/0.05 mL) (A solution). Distilled water (1 mg/0.95 mL) was subsequently added to the A solution (B solution, 1 mg/1 mL), in which 5% glacial acetic acid was contained in the B solution. Further, the B solution was diluted to a final concentration of 0.5% acetic acid with distilled water (stock solution), which was subcutaneously injected into the mice once a day at a dosage of 10 mL/kg for three days. Therefore, one injected dose would constitute 0.3 ml of Reserpine (stock solution) for a mouse with a body weight of 30 g.
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4

Reserpine-Induced Muscle Hyperalgesia Model

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The RIM model, which mimics features of FM, including hyperalgesic symptoms, was generated according to a previously reported method.10 (link) Reserpine, a CNS monoamine depleting substance (Nacalai Tesque Inc., Kyoto, Japan) was dissolved in glacial acetic acid and diluted to a final concentration of 0.5% with distilled water. Rats were administered repeated subcutaneous (SC) injections of 1 mg·kg−1 Reserpine 3 times (once daily, for 3 consecutive days). Drugs were evaluated using a muscle pressure test on Day 7 after the final injection of Reserpine. After the pre-drug muscle pressure test, Reserpine-treated rats were allocated to groups based on their muscle pressure threshold, with each group receiving either vehicle or a dose of the drug. The muscle pressure test was conducted again after administration of vehicle or the drug. Vehicle or ASP0819 was orally administered on Day 8, and the muscle pressure threshold was measured 4 h after administration.
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5

Reserpine-Induced Fibromyalgia Model in Rats

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A previously optimized regimen of Reserpine, i.e., 1 mg/kg, subcutaneous, once daily for 3 consecutive days [1] (link), was used to induce a fibromyalgia-like condition in rats. Reserpine (Nacalai Tesque, Kyoto, Japan) was weighed, transferred to a 1.5 mL microtube, and dissolved in glacial acetic acid (FUJIFILM Wako Pure Chemical Co., Osaka, Japan) with sonication. This solution was diluted in a test tube with distilled water, resulting in final concentration of 1 mg/mL Reserpine in 0.5% acetic acid. The injection of Reserpine was initiated when the body weight of animal was <300 g. The Reserpine solution was injected subcutaneously on the back of rats in a volume of 1 mL/kg (i.e., 1 mg Reserpine/kg). The injection was administered once daily for 3 consecutive days. Control animals were injected with vehicle (0.5% acetic acid, 1 mL/kg of body weight).
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