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Signals for nausea and emesis: Implications for models of upper gastrointestinal diseases

机译:恶心和呕吐的信号:对上消化道疾病模型的启示

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摘要

Nausea and vomiting are amongst the most common symptoms encountered in medicine as either symptoms of diseases or side effects of treatments. In a more biological setting they are also important components of an organism’s defences against ingested toxins. Identification of treatments for nausea and vomiting and reduction of emetic liability of new therapies has largely relied on the use of animal models, and although such models have proven invaluable in identification of the anti-emetic effects of both 5-hydroxytryptamine3 and neurokinin1 receptor antagonists selection of appropriate models is still a matter of debate. The present paper focuses on a number of controversial issues and gaps in our knowledge in the study of the physiology of nausea and vomiting including: The choice of species for the study of emesis and the underlying behavioural (e.g. neophobia), anatomical (e.g. elongated, narrow abdominal oesophagus with reduced ability to shorten) and physiological (e.g. brainstem circuitry) mechanisms that explain the lack of a vomiting reflex in certain species (e.g. rats); The choice of response to measure (emesis[retching and vomiting], conditioned flavour avoidance or aversion, ingestion of clay[pica], plasma hormone levels[e.g. vasopressin], gastric dysrhythmias) and the relationship of these responses to those observed in humans and especially to the sensation of nausea; The stimulus coding of nausea and emesis by abdominal visceral afferents and especially the vagus—how do the afferents encode information for normal postprandial sensations, nausea and finally vomiting?; Understanding the central processing of signals for nausea and vomiting is particularly problematic in the light of observations that vomiting is more readily amenable to pharmacological treatment than is nausea, despite the assumption that nausea represents “low” intensity activation of pathways that can evoke vomiting when stimulated more intensely.
机译:恶心和呕吐是医学上最常见的症状之一,无论是疾病症状还是治疗副作用。在更加生物学的环境中,它们也是有机体抵抗摄入毒素的重要组成部分。确定恶心和呕吐的治疗方法以及减少新疗法的催吐作用很大程度上依赖于动物模型的使用,尽管已证明这种模型对于鉴定5-羟色胺3和神经激肽1受体拮抗剂的镇吐作用具有重要价值。合适的模型仍然是一个争论的问题。本论文着重研究恶心和呕吐生理学方面的一些有争议的问题和我们知识上的空白,包括:用于研究呕吐和潜在行为(例如新恐惧症),解剖学(例如拉长的,腹壁狭窄的食管,具有缩短的能力降低和生理机制(例如脑干回路),这些机制可以解释某些物种(例如大鼠)缺乏呕吐反射;选择应对措施(呕吐[呕吐和呕吐],有条件的风味避免或厌恶,摄取黏土[pica],血浆激素水平[例如加压素],胃节律不全)以及这些响应与在人和人中观察到的响应之间的关系特别是恶心的感觉;腹腔内脏传入,特别是迷走神经的刺激编码,包括恶心和呕吐。传入的传入信号如何编码正常的餐后感觉,恶心和最终呕吐的信息?鉴于观察到呕吐比恶心更容易接受药理学治疗,因此了解恶心和呕吐信号的中央处理尤其成问题,尽管假设恶心代表“低”强度的激活途径,刺激后可引起呕吐。更强烈地。

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