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首页> 外文期刊>The Open Neuroscience Journal >Central Nervous System Circuitries Underlying Two Types of Peripheral Autonomic Nervous System Disorders
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Central Nervous System Circuitries Underlying Two Types of Peripheral Autonomic Nervous System Disorders

机译:两种类型的周围自主神经系统疾病的中枢神经系统回路

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The assessment of circulating neurotransmitters: noradrenaline, adrenaline, dopamine, platelet serotonin,plasma serotonin and plasma tryptophan before and after many types of stressor agents and neuropharmacological drugscarried out over the last thirty years allowed us to accumulate information dealing with the central nervous system (CNS)versus the peripheral autonomic nervous system (ANS) interactions in healthy as well as diseased mammals. Furthermore,the accurate knowledge about the CNS circuitry disorders which underlie both the CNS and peripheral clinical syndromes,has allowed us to prescribe successful neuropharmacological therapeutical strategies for many types of illnesses. In addition,the demonstration that the clinical improvement was always paralleled by the normalization of the neurochemical,hormonal, immunological and clinical profiles affords strong support to our point of view. According to all the above, theauthors postulate the existence of two types of diseases: type A and Type N, which are underlain by two opposite CNS +ANS disorders. Type A diseases should be associated with the "uncoping stress" syndrome and are underlain by hyperactivityof the adrenocortical glands plus the CNS disorder characterized by the predominance of the C1(adrenergic) +DR(serotonergic) axis over the A5(noradrenergic) + MR(serotonergic) binomial, whereas the type N diseases depends onthe opposite profile: "endogenous depression" syndrome. Finally, we quoted exhaustive evidence showing that the wellknown fading of both the A6(noradrenergic) + C1(adrenergic) CNS nuclei activity occurring during aging is responsiblefor the ANS + CNS disorder which is similar to that underlying psychosis, Alzheimer, post-traumatic stress disorder anddeficit-attention hyperactive disorder.
机译:在过去三十年进行的多种压力源和神经药理药物的治疗前后,对循环神经递质(去甲肾上腺素,肾上腺素,多巴胺,血小板5-羟色胺,血浆5-羟色胺和血浆色氨酸)的评估使我们能够积累有关中枢神经系统(CNS)的信息与健康和患病哺乳动物的周围自主神经系统(ANS)相互作用相比。此外,对中枢神经系统和周围临床综合症基础的中枢神经系统电路障碍的准确了解,使我们能够为多种疾病开出成功的神经药理学治疗策略。另外,临床改善总是与神经化学,激素,免疫学和临床特征正常化并行进行的证明为我们的观点提供了有力的支持。根据以上所有内容,作者推测存在两种类型的疾病:A型和N型,这是两种相对的CNS + ANS疾病所致。 A型疾病应与“解除压力”综合征相关,并以肾上腺皮质多动症和以C1(肾上腺素能)+ DR(5-羟色胺能)轴在A5(去甲肾上腺素能)+ MR(MR)上占优势的CNS疾病为基础。血清素能)二项式,而N型疾病则取决于相反的特征:“内源性抑郁症”综合征。最后,我们引用了详尽的证据,表明衰老期间发生的A6(去甲肾上腺素能)+ C1(肾上腺素能)中枢神经系统核衰变是导致ANS +中枢神经系统疾病的原因,这与潜在的精神病,阿尔茨海默病,创伤后应激相似障碍和注意力缺陷多动障碍。

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