Study of fingolimod, nitric oxide inhibitor, and P-glycoprotein inhibitor in modulating the P-glycoprotein expression via an endothelin-sphingolipid pathway in an animal model of pharmacoresistant epilepsy.

IF 1.4 4区 医学 Q4 PHARMACOLOGY & PHARMACY Indian Journal of Pharmacology Pub Date : 2023-09-01 DOI:10.4103/ijp.ijp_100_23
Nitika Garg, Rupa Joshi, Alka Bhatia, Seema Bansal, Amitava Chakrabarti, Ajay Prakash, Biman Saikia, Manish Modi, Bikash Medhi
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Abstract

Background: The overexpression of P-glycoprotein (P-gp) contributes to drug resistance in patients with epilepsy, and the change of P-gp expression located at the blood-brain barrier alienates the anti-seizure effects of P-gp substrates. Thus, the present study explored the effect of fingolimod (FTY720) acting through an endothelin-sphingolipid pathway on P-gp-induced pentylenetetrazol (PTZ)-kindled phenobarbital (PB)-resistant rats.

Materials and methods: PTZ kindling (30 mg/kg; i.p.) and PB (40 mg/kg; orally) were used to develop an animal model of refractory epilepsy. The effect of Fingolimod on seizure score (Racine scale), plasma and brain levels of PB (high-performance liquid chromatography), and blood-brain barrier permeability (Evans blue dye) was determined. Further, Fingolimod's neuroprotective effect was determined by measuring the levels of various inflammatory cytokines, oxidative stress parameters, and neurotrophic factors in rat brain homogenate. The Fingolimod's effect on P-gp expression was estimated by reverse transcriptase-polymerase chain reaction and immunohistochemistry in rat brain. The H and E staining was done to determine the neuronal injury.

Results: Fingolimod significantly (P < 0.001) reduced the seizure score in a dose-dependent manner and alleviated the blood-brain barrier permeability. It decreased the P-gp expression, which further increased the brain PB concentration. Fingolimod significantly (P < 0.01) reduced oxidative stress as well as inflammation. Moreover, it attenuated the raised neuronal injury score in a resistant model of epilepsy.

Conclusion: The modulation of the P-gp expression by Fingolimod improved drug delivery to the brain in an animal model of refractory epilepsy. Therefore, S1P signaling could serve as an additional therapeutic target to overcome refractoriness.

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fingolimod、一氧化氮抑制剂和P-糖蛋白抑制剂在耐药性癫痫动物模型中通过内皮素-鞘脂途径调节P-糖蛋白表达的研究。
背景:P-糖蛋白(P-gp)的过度表达导致癫痫患者的耐药性,而位于血脑屏障的P-gp表达的变化疏远了P-gp底物的抗癫痫作用。因此,本研究探讨了fingolimod(FTY720)通过内皮素-鞘脂途径对P-糖蛋白诱导的戊四氮(PTZ)点燃的苯巴比妥(PB)抗性大鼠的影响。材料和方法:PTZ点燃(30mg/kg;腹腔注射)和PB(40mg/kg;口服)建立难治性癫痫动物模型。测定芬戈利莫对癫痫发作评分(拉辛评分)、血浆和大脑PB(高效液相色谱法)水平以及血脑屏障通透性(埃文斯蓝染料)的影响。此外,通过测量大鼠脑匀浆中各种炎性细胞因子、氧化应激参数和神经营养因子的水平来确定芬戈利莫的神经保护作用。采用逆转录聚合酶链反应和免疫组织化学方法研究芬戈利莫对大鼠脑组织P-gp表达的影响。进行H和E染色以确定神经元损伤。结果:芬戈利莫能显著降低癫痫发作评分(P<0.001),并呈剂量依赖性,减轻血脑屏障通透性。它降低了P-gp的表达,从而进一步增加了脑内PB的浓度。芬戈利莫能显著降低氧化应激和炎症反应(P<0.01)。此外,它减轻了癫痫抵抗模型中神经元损伤评分的升高。结论:芬戈利莫对P-gp表达的调节改善了难治性癫痫动物模型中药物向大脑的递送。因此,S1P信号传导可以作为克服难治性的额外治疗靶点。
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来源期刊
CiteScore
4.00
自引率
4.20%
发文量
53
审稿时长
4-8 weeks
期刊介绍: Indian Journal of Pharmacology accepts, in English, review articles, articles for educational forum, original research articles (full length and short communications), letter to editor, case reports and interesting fillers. Articles concerning all aspects of pharmacology will be considered. Articles of general interest (e.g. methods, therapeutics, medical education, interesting websites, new drug information and commentary on a recent topic) are also welcome.
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