大鼠味觉联想学习:环孢素A条件免疫抑制研究神经免疫网络。

Current Protocols Pub Date : 2022-10-01 DOI:10.1002/cpz1.573
Stephan Leisengang, Manfred Schedlowski, Martin Hadamitzky, Laura Lückemann
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引用次数: 0

摘要

免疫抑制药物的药理作用,如环孢素A (CsA),可以通过应用联想学习范式被人类和动物学习和检索。这一原则基于巴甫洛夫条件反射,即反复呈现“无条件刺激”(美国;在这里,药物CsA与暴露于“条件刺激”(CS;这里,糖精的新奇味道)。在较晚的时间再次接触CS会导致回避行为。同时,使用这种模式,暴露于CS(糖精)的动物表现出免疫抑制,反映在脾脏t细胞增殖减少,体外培养的脾细胞中白细胞介素-2和干扰素-γ的表达和释放减少,模仿US (CsA)的药理作用。值得注意的是,这种味觉免疫联想学习的范例展示了大脑检测和存储有关生物体免疫状态的信息并检索这些信息的令人印象深刻的能力,从而通过内源性途径调节免疫功能。此外,通过联想学习获得的条件性药理效应已经成功地作为控制药物剂量减少策略作为一种支持治疗选择来优化药物治疗效果,以使患者受益。然而,我们对介导这种习得性免疫调节作用的潜在神经生物学和免疫学机制的了解仍然有限。一个可靠的味觉免疫联想学习的动物模型可以为周围和中枢神经过程提供新的见解。在本文中,我们描述了在大鼠中使用CsA和糖精的基本味觉免疫联想学习范式的方案,其中在体外培养的脾细胞中确定了条件外周免疫抑制。该行为协议是可靠的和适应性强的,可能为未来使用味觉免疫联想学习范式的研究铺平道路,以更深入地了解脑-免疫系统的交流。©2022作者。Wiley期刊有限责任公司发表的当前方案:基本方案1:环孢素A的味觉免疫联想学习基本方案2:脾细胞分离和培养以研究刺激诱导的细胞因子产生。
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Taste-Associative Learning in Rats: Conditioned Immunosuppression with Cyclosporine A to Study the Neuro-Immune Network.

The pharmacological effects of an immunosuppressive drug, such as cyclosporine A (CsA), can be learned and retrieved by humans and animals when applying associative learning paradigms. This principle is based on Pavlovian conditioning, in which repeated presentation of an "unconditioned stimulus" (US; here, the drug CsA) is paired with exposure to a "conditioned stimulus" (CS; here, the novel taste of saccharin). Re-exposure to the CS at a later time leads to an avoidance behavior. Concomitantly, using this paradigm, animals exposed to the CS (saccharin) display immunosuppression, reflected by reduced splenic T-cell proliferation and diminished interleukin-2 and interferon-γ expression and release in ex vivo cultured splenocytes, mimicking the pharmacological effects of the US (CsA). Notably, this paradigm of taste-immune associative learning demonstrates the impressive abilities of the brain to detect and store information about an organism's immunological status and to retrieve this information, thereby modulating immunological functions via endogenous pathways. Moreover, conditioned pharmacological effects, obtained by means of associative learning, have been successfully implemented as controlled drug-dose reduction strategies as a supportive treatment option to optimize pharmacological treatment effects for patients' benefit. However, our knowledge about the underlying neurobiological and immunological mechanisms mediating such learned immunomodulatory effects is still limited. A reliable animal model of taste-immune associative learning can provide novel insights into peripheral and central nervous processes. In this article, we describe protocols that focus on the basic taste-immune associative learning paradigm with CsA and saccharin in rats, where conditioned peripheral immunosuppression is determined in ex vivo cultured splenocytes. The behavioral protocol is reliable and adaptable and may pave the road for future studies using taste-immune associative learning paradigms to gain deeper insight into brain-to-immune-system communication. © 2022 The Authors. Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Taste-immune associative learning with cyclosporine A Basic Protocol 2: Splenocyte isolation and cultivation to study stimulation-induced cytokine production.

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