Holanda Victor A D, Didonet Julia J, Costa Manara B B, do Nascimento Rangel Adriano H, da Silva Edilson D, Gavioli Elaine C
Department of Biophysics and Pharmacology, Federal University of Rio Grande do Norte, Natal, RN 59078-900, Brazil.
Agricultural School of Jundiaì, Federal University of Rio Grande do Norte, Macaíba, RN 59280-000, Brazil.
Pharmaceuticals (Basel). 2021 Aug 6;14(8):775. doi: 10.3390/ph14080775.
Parkinson disease (PD) is a neurodegenerative disease mainly characterized by the loss of nigral dopaminergic neurons in the substantia nigra pars compacta. Patients suffering from PD develop severe motor dysfunctions and a myriad of non-motor symptoms. The treatment mainly consists of increasing central dopaminergic neurotransmission and alleviating motor symptoms, thus promoting severe side effects without modifying the disease's progress. A growing body of evidence suggests a close relationship between neuropeptide S (NPS) and its receptor (NPSR) system in PD: (i) double immunofluorescence labeling studies showed that NPSR is expressed in the nigral tyrosine hydroxylase (TH)-positive neurons; (ii) central administration of NPS increases spontaneous locomotion in naïve rodents; (iii) central administration of NPS ameliorates motor and nonmotor dysfunctions in animal models of PD; (iv) microdialysis studies showed that NPS stimulates dopamine release in naïve and parkinsonian rodents; (v) central injection of NPS decreases oxidative damage to proteins and lipids in the rodent brain; and, (vi) 7 days of central administration of NPS protects from the progressive loss of nigral TH-positive cells in parkinsonian rats. Taken together, the NPS/NPSR system seems to be an emerging therapeutic strategy for alleviating motor and non-motor dysfunctions of PD and, possibly, for slowing disease progress.
帕金森病(PD)是一种神经退行性疾病,主要特征是黑质致密部的黑质多巴胺能神经元丧失。帕金森病患者会出现严重的运动功能障碍和众多非运动症状。治疗主要包括增加中枢多巴胺能神经传递和缓解运动症状,从而在不改变疾病进展的情况下引发严重的副作用。越来越多的证据表明神经肽S(NPS)及其受体(NPSR)系统在帕金森病中存在密切关系:(i)双重免疫荧光标记研究表明,NPSR在黑质酪氨酸羟化酶(TH)阳性神经元中表达;(ii)向未处理的啮齿动物中枢给予NPS可增加自发运动;(iii)向帕金森病动物模型中枢给予NPS可改善运动和非运动功能障碍;(iv)微透析研究表明,NPS可刺激未处理和帕金森病啮齿动物的多巴胺释放;(v)向啮齿动物脑内中央注射NPS可减少蛋白质和脂质的氧化损伤;以及,(vi)连续7天向帕金森病大鼠中枢给予NPS可防止黑质TH阳性细胞的逐渐丧失。综上所述,NPS/NPSR系统似乎是一种新兴的治疗策略,可用于缓解帕金森病的运动和非运动功能障碍,并可能减缓疾病进展。