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过氧化物酶体增殖物激活受体γ(PPARγ)激动剂吡格列酮对与手术切口、周围神经损伤及疼痛性糖尿病神经病变相关的痛觉过敏具有以女性为主的抑制作用。

The PPARγ agonist pioglitazone produces a female-predominant inhibition of hyperalgesia associated with surgical incision, peripheral nerve injury, and painful diabetic neuropathy.

作者信息

Santos D F S, Donahue R R, Laird D E, Oliveira M C G, Taylor B K

机构信息

Department of Anesthesiology and Perioperative Medicine, Pittsburgh Center for Pain Research, and Pittsburgh Project to End Opioid Misuse, University of Pittsburgh, Pittsburgh, PA, USA; School of Applied Sciences, State University of Campinas-UNICAMP, Limeira, SP, Brazil.

Department of Physiology, University of Kentucky Medical Center, Lexington, KY, USA.

出版信息

Neuropharmacology. 2022 Mar 1;205:108907. doi: 10.1016/j.neuropharm.2021.108907. Epub 2021 Nov 29.

Abstract

Pioglitazone, an agonist at peroxisome proliferator-activated receptor gamma, is FDA-approved for the treatment of insulin resistance in type 2 diabetes. Numerous studies in male rodents suggest that pioglitazone inhibits inflammatory and neuropathic pain, but few included female subjects. To address this gap, we compared the effects of pioglitazone in both sexes in the intraplantar methylglyoxal model (MG) model of chemical pain and painful diabetic neuropathy (PDN), the plantar incision model (PIM) of postoperative pain, the spared nerve injury (SNI) model of traumatic nerve injury, and the ZDF rat and db/db mouse models of PDN. We administered pioglitazone by one-time intrathecal or intraperitoneal injection or by adding it to chow for 6 weeks, followed by measurement of hypersensitivity to non-noxious mechanical, noxious mechanical, heat, and/or cold stimuli. In all mouse models, injection of pioglitazone decreased pain-like behaviors with greater potency and/or efficacy in females as compared to males: heat and mechanical hypersensitivity in the MG model (0.1-10 mg/kg); mechanical hypersensitivity in the PIM model (10 μg); mechanical and cold hypersensitivity in the SNI model (100 mg/kg); and heat hypersensitivity in the db/db model (100 mg/kg). Furthermore, co-administration of low doses of morphine (1 mg/kg) and pioglitazone (10 mg/kg) decreased SNI-induced mechanical and cold hypersensitivity in female but not male mice. In the ZDF rat, pioglitazone (100 mg/kg) decreased heat and mechanical hypersensitivity with no sex difference. In the db/db model, pioglitazone had no effect when given into chow for 6 weeks at 0.3, 3 or 30 mg/kg doses. We conclude that females exhibit greater anti-hyperalgesic responses to pioglitazone in mouse models of chemical-induced nociception, postsurgical pain, neuropathic pain, and PDN. These findings set the stage for clinical trials to determine whether pioglitazone has analgesic properties across a broad spectrum of chronic pain conditions, particularly in women.

摘要

吡格列酮是过氧化物酶体增殖物激活受体γ的激动剂,已获美国食品药品监督管理局(FDA)批准用于治疗2型糖尿病中的胰岛素抵抗。在雄性啮齿动物中进行的大量研究表明,吡格列酮可抑制炎性疼痛和神经性疼痛,但纳入女性受试者的研究较少。为填补这一空白,我们比较了吡格列酮在化学性疼痛和糖尿病性疼痛性神经病变(PDN)的足底内甲基乙二醛模型(MG模型)、术后疼痛的足底切口模型(PIM)、创伤性神经损伤的 spared 神经损伤(SNI)模型以及PDN的ZDF大鼠和db/db小鼠模型中对两性的影响。我们通过一次性鞘内或腹腔注射给予吡格列酮,或将其添加到食物中持续6周,随后测量对非伤害性机械刺激、伤害性机械刺激、热刺激和/或冷刺激的超敏反应。在所有小鼠模型中,与雄性相比,注射吡格列酮可降低雌性小鼠的疼痛样行为,且效力和/或效果更佳:在MG模型中对热和机械刺激的超敏反应(0.1 - 10mg/kg);在PIM模型中对机械刺激的超敏反应(10μg);在SNI模型中对机械和冷刺激的超敏反应(100mg/kg);在db/db模型中对热刺激的超敏反应(100mg/kg)。此外,联合给予低剂量吗啡(1mg/kg)和吡格列酮(10mg/kg)可降低雌性而非雄性小鼠中SNI诱导的机械和冷刺激超敏反应。在ZDF大鼠中,吡格列酮(100mg/kg)可降低热和机械刺激超敏反应,且无性别差异。在db/db模型中,以0.3、3或30mg/kg的剂量添加到食物中6周时,吡格列酮无作用。我们得出结论,在化学诱导的伤害感受、术后疼痛、神经性疼痛和PDN的小鼠模型中,雌性对吡格列酮表现出更强的抗痛觉过敏反应。这些发现为临床试验奠定了基础,以确定吡格列酮是否在广泛的慢性疼痛病症中具有镇痛特性,尤其是在女性中。

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