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腺苷信号对戊四氮诱导斑马鱼记忆损伤的影响

The Effect of Adenosine Signaling on Memory Impairment Induced by Pentylenetetrazole in Zebrafish.

作者信息

Bertoncello Kanandra Taisa, Bonan Carla Denise

机构信息

Laboratório de Neuroquímica e Psicofarmacologia, Programa de Pós-Graduação em Biologia Celular e Molecular, Escola de Ciências da Saúde e da Vida, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, RS, Brazil.

Programa de Pós-Graduação em Medicina e Ciências da Saúde, Escola de Medicina, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, RS, Brazil.

出版信息

Neurochem Res. 2023 Jun;48(6):1889-1899. doi: 10.1007/s11064-023-03867-2. Epub 2023 Feb 2.

Abstract

Epilepsy is characterized by the manifestation of spontaneous and recurrent seizures. The high prevalence of comorbidities associated with epilepsy, such as cognitive dysfunction, affects the patients quality of life. Adenosine signaling modulation might be an effective alternative to control seizures and epilepsy-associated comorbidities. This study aimed to verify the role of adenosine modulation on the seizure development and cognitive impairment induced by pentylenetetrazole (PTZ) in zebrafish. At first, animals were submitted to a training session in the inhibitory avoidance test and, after 10 min, they received an intraperitoneal injection of valproate, adenosine A receptor agonist cyclopentyladenosine (CPA), adenosine A receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX), adenosine A receptor antagonist ZM 241385, adenosine deaminase inhibitor erythro-9-(2-hydroxy-3-nony1)-adenine hydrochloride (EHNA) or the nucleoside transporter inhibitor dipyridamole. Thirty min after the intraperitoneal injection, the animals were exposed to 7.5 mM PTZ for 10 min, where they were evaluated for latency to reach the seizure stages (I, II, and III). Finally, 24 h after the training session, the animals were submitted to the inhibitory avoidance test to verify their cognitive performance during the test session. Valproate, CPA, and EHNA showed antiseizure effects and prevented the memory impairment induced by PTZ exposure. DPCPX, ZM 241385, and dipyridamole pretreatments caused no changes in seizure development; however, these drugs prevented memory impairment without altering locomotion. Our results reinforce the antiseizure effects of adenosine signaling and support the idea that the involvement of adenosine in memory processes may be a target for preventive strategies against cognitive impairment associated with epilepsy.

摘要

癫痫的特征是自发和反复发作性癫痫发作。与癫痫相关的合并症(如认知功能障碍)的高患病率影响患者的生活质量。腺苷信号调节可能是控制癫痫发作和癫痫相关合并症的有效替代方法。本研究旨在验证腺苷调节在戊四氮(PTZ)诱导的斑马鱼癫痫发作发展和认知障碍中的作用。首先,动物在抑制性回避试验中接受训练,10分钟后,它们接受腹腔注射丙戊酸、腺苷A受体激动剂环戊腺苷(CPA)、腺苷A受体拮抗剂8-环戊基-1,3-二丙基黄嘌呤(DPCPX)、腺苷A受体拮抗剂ZM 241385、腺苷脱氨酶抑制剂盐酸erythro-9-(2-羟基-3-壬基)-腺嘌呤(EHNA)或核苷转运体抑制剂双嘧达莫。腹腔注射30分钟后,动物暴露于7.5 mM PTZ中10分钟,在此期间评估它们达到癫痫发作阶段(I、II和III)的潜伏期。最后,在训练后24小时,动物接受抑制性回避试验,以验证它们在试验期间的认知表现。丙戊酸、CPA和EHNA显示出抗癫痫作用,并预防了PTZ暴露引起的记忆损害。DPCPX、ZM 241385和双嘧达莫预处理对癫痫发作发展没有影响;然而,这些药物在不改变运动的情况下预防了记忆损害。我们的结果强化了腺苷信号的抗癫痫作用,并支持腺苷参与记忆过程可能是预防癫痫相关认知障碍的策略靶点这一观点。

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