传统的高脂肪/高碳水化合物饮食或生酮饮食对雌性大鼠吗啡敏感性的影响。

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacology and Experimental Therapeutics Pub Date : 2024-09-18 DOI:10.1124/jpet.124.002188
Nina M Beltran, Alyssa N Parra, Ana Paulina Serrano, Jazmin Castillo, Isabella M Castro, Madeline K Elsey, Vanessa Minervini, Katherine M Serafine
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引用次数: 0

摘要

被诊断为肥胖症的患者服用阿片类药物的比例高于普通人群;然而,高脂肪饮食是否会影响个人对这些药物的敏感性尚不得而知。为了探索 "高脂肪饮食会增加大鼠对吗啡的敏感性 "这一假设,24 只雌性 Sprague-Dawley 大鼠(n=8/diet)分别进食了标准实验室饲料(17% 千卡热量来自脂肪)、高脂肪/低碳水化合物(生酮)饲料(90.5% 千卡热量来自脂肪)或传统高脂肪/高碳水化合物饲料(60% 千卡热量来自脂肪)。吗啡诱导的抗镇痛作用是通过温水尾部抽离程序进行评估的。在该程序中,记录大鼠在注射生理盐水或吗啡(0.32-56 毫克/千克,IP)后将尾部从温水浴中抽出的潜伏期(以秒为单位)。对大鼠进行急性和慢性吗啡注射,每天注射两次,为期19天(每3天以1/4对数剂量递增:3.2-56毫克/千克,IP),以诱导大鼠对吗啡产生依赖性并评估耐受性。在整个研究过程中,对吗啡的不良反应(即耐受性、戒断、体温变化)进行了评估。吗啡对食用不同食物的大鼠产生了类似的抗痛作用,所有大鼠在长期接触吗啡后都产生了耐受性。吗啡的其他不良反应在食用不同食物的大鼠中也具有可比性;然而,食用生酮饲料的大鼠因戒断引起的体重减轻程度较轻。这些结果表明,饮食控制可能会调节戒断相关体重减轻的严重程度,其方式可能与患者相关。意义声明 本项针对雌性大鼠的研究表明,食用高脂肪/低碳水化合物(生酮饮食)或传统的高脂肪/高碳水化合物饮食不会影响阿片类药物的镇痛或不良反应(即耐受或戒断)。不过,生酮饮食可能对阿片类药物戒断相关的体重减轻有好处。因此,因疼痛相关疾病而服用阿片类药物的肥胖症患者在停止服用阿片类药物时,可考虑采用生酮饮食,以减轻因戒断阿片类药物而导致的体重减轻。
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The Effects of Eating a Traditional High Fat/High Carbohydrate or a Ketogenic Diet on Sensitivity of Female Rats to Morphine.

Patients diagnosed with obesity are prescribed opioid medications at a higher rate than the general population; however, it is not known if eating a high fat diet might impact individual sensitivity to these medications. To explore the hypothesis that eating a high fat diet increases sensitivity of rats to the effects of morphine, 24 female Sprague-Dawley rats (n = 8/diet) ate either a standard (low fat) laboratory chow (17% kcal from fat), a high fat/low carbohydrate (ketogenic) chow (90.5% kcal from fat), or a traditional high fat/high carbohydrate chow (60% kcal from fat). Morphine-induced antinociception was assessed using a warm water tail withdrawal procedure, during which latency (in seconds) for rats to remove their tail from warm water baths was recorded following saline or morphine (0.32-56 mg/kg, i.p.) injections. Morphine was administered acutely and chronically (involving 18 days of twice-daily injections, increasing in 1/4 log dose increments every 3 days: 3.2-56 mg/kg, i.p., to induce dependence and assess tolerance). The adverse effects of morphine (i.e., tolerance, withdrawal, and changes in body temperature) were assessed throughout the study. Acute morphine induced comparable antinociception in rats eating different diets, and all rats developed tolerance following chronic morphine exposure. Observable withdrawal signs and body temperature were also comparable among rats eating different diets; however, withdrawal-induced weight loss was less severe for rats eating ketogenic chow. These results suggest that dietary manipulation might modulate the severity of withdrawal-related weight loss in ways that could be relevant for patients.

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来源期刊
CiteScore
6.90
自引率
0.00%
发文量
115
审稿时长
1 months
期刊介绍: A leading research journal in the field of pharmacology published since 1909, JPET provides broad coverage of all aspects of the interactions of chemicals with biological systems, including autonomic, behavioral, cardiovascular, cellular, clinical, developmental, gastrointestinal, immuno-, neuro-, pulmonary, and renal pharmacology, as well as analgesics, drug abuse, metabolism and disposition, chemotherapy, and toxicology.
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