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BPC 157、L-硝基精氨酸甲酯、L-精氨酸、与一氧化氮无关,在类似于精神分裂症“阴性样”症状的适宜大鼠氯胺酮模型中。

BPC 157, L-NAME, L-Arginine, NO-Relation, in the Suited Rat Ketamine Models Resembling "Negative-Like" Symptoms of Schizophrenia.

作者信息

Zemba Cilic Andrea, Zemba Mladen, Cilic Matija, Strbe Sanja, Ilic Spomenko, Vukojevic Jaksa, Zoricic Zoran, Filipcic Igor, Kokot Antonio, Smoday Ivan Maria, Rukavina Iva, Boban Blagaic Alenka, Tvrdeic Ante, Duplancic Bozidar, Stambolija Vasilije, Marcinko Darko, Skrtic Anita, Seiwerth Sven, Sikiric Predrag

机构信息

Department of Pharmacology, School of Medicine, University of Zagreb, 10000 Zagreb, Croatia.

Department of Psychiatry, University of Zagreb School of Medicine, University Clinical Centre Zagreb, 10000 Zagreb, Croatia.

出版信息

Biomedicines. 2022 Jun 21;10(7):1462. doi: 10.3390/biomedicines10071462.

Abstract

We attempted throughout the NO-system to achieve the particular counteraction of the ketamine-induced resembling "negative-like" schizophrenia symptoms in rats using pentadecapeptide BPC 157, and NO-agents, NG-nitro-L-arginine methylester (L-NAME), and/or L-arginine, triple application. This might be the find out the NO-system organized therapy (i.e., simultaneously implied NO-system blockade (L-NAME) vs. NO-system over-stimulation (L-arginine) vs. NO-system immobilization (L-NAME+L-arginine)). The ketamine regimen (intraperitoneally/kg) included: 3 mg (cognitive dysfunction, novel object recognition test), 30 mg (anxiogenic effect (open field test) and anhedonia (sucrose test)), and 8 mg/3 days (social withdrawal). Medication (mg/kg intraperitoneally) was L-NAME (5), L-arginine (100), and BPC 157 (0.01), alone and/or together, given immediately before ketamine (L-NAME, L-arginine, and combination) or given immediately after (BPC 157 and combinations). BPC 157 counteracted ketamine-cognition dysfunction, social withdrawal, and anhedonia, and exerted additional anxiolytic effect. L-NAME (antagonization, social withdrawal) and L-arginine (antagonization, cognitive dysfunction, anhedonia) both included worsening cognitive dysfunction, anhedonia, and anxiogenic effect (L-NAME), social withdrawal, and anxiogenic effect (L-arginine). Thus, ketamine-induced resembling "negative-like" schizophrenia symptoms were "L-NAME non-responsive, L-arginine responsive" (cognition dysfunction), "L-NAME responsive, L-arginine non-responsive" (social withdrawal), "L-NAME responsive, L-arginine responsive, opposite effect" (anhedonia) and "L-NAME responsive, L-arginine responsive, parallel effect" (both anxiogening). In cognition dysfunction, BPC 157 overwhelmed NO-agents effects. The mRNA expression studies in brain tissue evidenced considerable overlapping of gene overexpression in healthy rats treated with ketamine or BPC 157. With the BPC 157 therapy applied immediately after ketamine, the effect on , , , , and (increased or decreased expression), appeared as a timely specific BPC 157 effect on ketamine-specific targets.

摘要

我们试图在整个一氧化氮(NO)系统中,通过使用十五肽BPC 157以及NO制剂(NG-硝基-L-精氨酸甲酯(L-NAME)和/或L-精氨酸)联合应用,来对抗氯胺酮诱导的大鼠类似“阴性样”精神分裂症症状。这可能是为了找出针对NO系统的有组织的治疗方法(即同时进行NO系统阻断(L-NAME)、NO系统过度刺激(L-精氨酸)或NO系统固定(L-NAME + L-精氨酸))。氯胺酮给药方案(腹腔注射/千克)包括:3毫克(认知功能障碍,新物体识别测试)、30毫克(致焦虑作用(旷场试验)和快感缺失(蔗糖试验))以及8毫克/3天(社交退缩)。药物(腹腔注射毫克/千克)为L-NAME(5)、L-精氨酸(100)和BPC 157(0.01),单独使用和/或联合使用,在氯胺酮给药前即刻给予(L-NAME、L-精氨酸及其组合)或在给药后即刻给予(BPC 157及其组合)。BPC 157对抗了氯胺酮引起的认知功能障碍、社交退缩和快感缺失,并产生了额外的抗焦虑作用。L-NAME(对抗社交退缩)和L-精氨酸(对抗认知功能障碍、快感缺失)均加重了认知功能障碍、快感缺失以及致焦虑作用(L-NAME)、社交退缩和致焦虑作用(L-精氨酸)。因此,氯胺酮诱导的类似“阴性样”精神分裂症症状呈现出“L-NAME无反应、L-精氨酸有反应”(认知功能障碍)、“L-NAME有反应、L-精氨酸无反应”(社交退缩)、“L-NAME有反应、L-精氨酸有反应,作用相反”(快感缺失)以及“L-NAME有反应、L-精氨酸有反应,作用平行”(两者均有致焦虑作用)。在认知功能障碍方面,BPC 157抵消了NO制剂的作用。脑组织中的mRNA表达研究表明,用氯胺酮或BPC 157处理的健康大鼠中基因过表达存在相当程度的重叠。在氯胺酮给药后即刻应用BPC 157治疗,对 、 、 、 和 (表达增加或减少)的影响,表现为BPC 157对氯胺酮特异性靶点的及时特异性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c183/9313087/8c84d5967860/biomedicines-10-01462-g001.jpg

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