MDMA Impairs Response to Water Intake in Healthy Volunteers.

Q1 Pharmacology, Toxicology and Pharmaceutics Advances in Pharmacological Sciences Pub Date : 2016-01-01 Epub Date: 2016-06-14 DOI:10.1155/2016/2175896
Matthew J Baggott, Kathleen J Garrison, Jeremy R Coyle, Gantt P Galloway, Allan J Barnes, Marilyn A Huestis, John E Mendelson
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Abstract

Hyponatremia is a serious complication of 3,4-methylenedioxymethamphetamine (MDMA) use. We investigated potential mechanisms in two double-blind, placebo-controlled studies. In Study 1, healthy drug-experienced volunteers received MDMA or placebo alone and in combination with the alpha-1 adrenergic inverse agonist prazosin, used as a positive control to release antidiuretic hormone (ADH). In Study 2, volunteers received MDMA or placebo followed by standardized water intake. MDMA lowered serum sodium but did not increase ADH or copeptin, although the control prazosin did increase ADH. Water loading reduced serum sodium more after MDMA than after placebo. There was a trend for women to have lower baseline serum sodium than men, but there were no significant interactions with drug condition. Combining studies, MDMA potentiated the ability of water to lower serum sodium. Thus, hyponatremia appears to be a significant risk when hypotonic fluids are consumed during MDMA use. Clinical trials and events where MDMA use is common should anticipate and mitigate this risk.

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亚甲二氧基甲基苯丙胺会影响健康志愿者对摄入水分的反应。
低钠血症是使用 3,4-亚甲二氧基甲基苯丙胺(MDMA)的一种严重并发症。我们在两项双盲安慰剂对照研究中调查了其潜在机制。在研究 1 中,有吸毒经验的健康志愿者单独或与作为阳性对照释放抗利尿激素(ADH)的α-1 肾上腺素能反向激动剂哌唑嗪联合服用了摇头丸或安慰剂。在研究 2 中,志愿者先服用摇头丸或安慰剂,然后摄入标准水。摇头丸降低了血清钠,但并没有增加促肾上腺皮质激素或促肾上腺皮质激素,尽管对照药哌唑嗪确实增加了促肾上腺皮质激素。与服用安慰剂相比,服用摇头丸后饮水更能降低血清钠。女性的基线血清钠有低于男性的趋势,但与药物条件没有明显的相互作用。综合各项研究,亚甲二氧基甲基苯丙胺增强了水降低血清钠的能力。因此,使用亚甲二氧基甲基苯丙胺期间饮用低渗液体时,低钠血症似乎是一个重大风险。使用亚甲二氧基甲基苯丙胺的临床试验和活动应预见并降低这种风险。
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来源期刊
Advances in Pharmacological Sciences
Advances in Pharmacological Sciences PHARMACOLOGY & PHARMACY-
CiteScore
6.40
自引率
0.00%
发文量
0
审稿时长
14 weeks
期刊介绍: Advances in Pharmacological and Pharmaceutical Sciences is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies in all areas of experimental and clinical pharmacology, pharmaceutics, medicinal chemistry and drug delivery. Topics covered by the journal include, but are not limited to: -Biochemical pharmacology, drug mechanism of action, pharmacodynamics, pharmacogenetics, pharmacokinetics, and toxicology. -The design and preparation of new drugs, and their safety and efficacy in humans, including descriptions of drug dosage forms. -All areas of medicinal chemistry, such as drug discovery, design and synthesis. -Basic biology of drug and gene delivery through to application and development of these principles, through therapeutic delivery and targeting. Areas covered include bioavailability, controlled release, microcapsules, novel drug delivery systems, personalized drug delivery, and techniques for passing biological barriers.
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