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对Wistar大鼠重复给予临床相关剂量的处方阿片类药物曲马多和氨酚羟考酮会导致肺、心脏和脑毒性。

Repeated Administration of Clinically Relevant Doses of the Prescription Opioids Tramadol and Tapentadol Causes Lung, Cardiac, and Brain Toxicity in Wistar Rats.

作者信息

Barbosa Joana, Faria Juliana, Garcez Fernanda, Leal Sandra, Afonso Luís Pedro, Nascimento Ana Vanessa, Moreira Roxana, Pereira Frederico C, Queirós Odília, Carvalho Félix, Dinis-Oliveira Ricardo Jorge

机构信息

IINFACTS-Institute of Research and Advanced Training in Health Sciences and Technologies, Department of Sciences, University Institute of Health Sciences (IUCS), CESPU, CRL, 4585-116 Gandra, Portugal.

UCIBIO, REQUIMTE-Laboratory of Toxicology, Department of Biological Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.

出版信息

Pharmaceuticals (Basel). 2021 Jan 27;14(2):97. doi: 10.3390/ph14020097.

Abstract

Tramadol and tapentadol, two structurally related synthetic opioid analgesics, are widely prescribed due to the enhanced therapeutic profiles resulting from the synergistic combination between μ-opioid receptor (MOR) activation and monoamine reuptake inhibition. However, the number of adverse reactions has been growing along with their increasing use and misuse. The potential toxicological mechanisms for these drugs are not completely understood, especially for tapentadol, owing to its shorter market history. Therefore, in the present study, we aimed to comparatively assess the putative lung, cardiac, and brain cortex toxicological damage elicited by the repeated exposure to therapeutic doses of both prescription opioids. To this purpose, male Wistar rats were intraperitoneally injected with single daily doses of 10, 25, and 50 mg/kg tramadol or tapentadol, corresponding to a standard analgesic dose, an intermediate dose, and the maximum recommended daily dose, respectively, for 14 consecutive days. Such treatment was found to lead mainly to lipid peroxidation and inflammation in lung and brain cortex tissues, as shown through augmented thiobarbituric acid reactive substances (TBARS), as well as to increased serum inflammation biomarkers, such as C reactive protein (CRP) and tumor necrosis factor-α (TNF-α). Cardiomyocyte integrity was also shown to be affected, since both opioids incremented serum lactate dehydrogenase (LDH) and α-hydroxybutyrate dehydrogenase (α-HBDH) activities, while tapentadol was associated with increased serum creatine kinase muscle brain (CK-MB) isoform activity. In turn, the analysis of metabolic parameters in brain cortex tissue revealed increased lactate concentration upon exposure to both drugs, as well as augmented LDH and creatine kinase (CK) activities following tapentadol treatment. In addition, pneumo- and cardiotoxicity biomarkers were quantified at the gene level, while neurotoxicity biomarkers were quantified both at the gene and protein levels; changes in their expression correlate with the oxidative stress, inflammatory, metabolic, and histopathological changes that were detected. Hematoxylin and eosin (H & E) staining revealed several histopathological alterations, including alveolar collapse and destruction in lung sections, inflammatory infiltrates, altered cardiomyocytes and loss of striation in heart sections, degenerated neurons, and accumulation of glial and microglial cells in brain cortex sections. In turn, Masson's trichrome staining confirmed fibrous tissue deposition in cardiac tissue. Taken as a whole, these results show that the repeated administration of both prescription opioids extends the dose range for which toxicological injury is observed to lower therapeutic doses. They also reinforce previous assumptions that tramadol and tapentadol are not devoid of toxicological risk even at clinical doses.

摘要

曲马多和他喷他多是两种结构相关的合成阿片类镇痛药,由于μ-阿片受体(MOR)激活与单胺再摄取抑制之间的协同组合产生了增强的治疗效果,因而被广泛处方用药。然而,随着它们使用和滥用的增加,不良反应的数量也在不断增长。由于他喷他多的上市时间较短,这些药物潜在的毒理学机制尚未完全明确,尤其是他喷他多。因此,在本研究中,我们旨在比较评估重复暴露于治疗剂量的这两种处方阿片类药物所引发的假定的肺、心脏和脑皮质毒理学损伤。为此,雄性Wistar大鼠连续14天每天腹腔注射10、25和50mg/kg的曲马多或他喷他多,分别对应标准镇痛剂量、中间剂量和最大推荐日剂量。结果发现,这种治疗主要导致肺和脑皮质组织中的脂质过氧化和炎症,这通过硫代巴比妥酸反应性物质(TBARS)增加得以体现,同时血清炎症生物标志物如C反应蛋白(CRP)和肿瘤坏死因子-α(TNF-α)也增加。心肌细胞完整性也显示受到影响,因为两种阿片类药物均增加了血清乳酸脱氢酶(LDH)和α-羟丁酸脱氢酶(α-HBDH)的活性,而他喷他多与血清肌酸激酶同工酶脑型(CK-MB)活性增加有关。反过来,对脑皮质组织代谢参数的分析显示,暴露于两种药物后乳酸浓度增加,他喷他多治疗后LDH和肌酸激酶(CK)活性增强。此外,在基因水平对肺毒性和心脏毒性生物标志物进行了定量,而在基因和蛋白质水平对神经毒性生物标志物进行了定量;它们表达的变化与检测到的氧化应激、炎症、代谢和组织病理学变化相关。苏木精和伊红(H&E)染色显示了几种组织病理学改变,包括肺切片中的肺泡塌陷和破坏、炎症浸润、心脏切片中改变的心肌细胞和横纹消失、神经元变性以及脑皮质切片中神经胶质细胞和小胶质细胞的积聚。反过来,Masson三色染色证实了心脏组织中有纤维组织沉积。总体而言,这些结果表明,重复给予这两种处方阿片类药物会将观察到毒理学损伤的剂量范围扩展至更低的治疗剂量。它们还强化了先前的假设,即即使在临床剂量下,曲马多和他喷他多也并非没有毒理学风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2495/7912343/2a0c8316d0b3/pharmaceuticals-14-00097-g001.jpg

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