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首页> 外文期刊>Toxins >Revisiting the Therapeutic Potential of Bothrops jararaca Venom: Screening for Novel Activities Using Connectivity Mapping
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Revisiting the Therapeutic Potential of Bothrops jararaca Venom: Screening for Novel Activities Using Connectivity Mapping

机译:再次探讨杂种植物茄子毒液的治疗潜力:使用连接映射筛选新活动。

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Snake venoms are sources of molecules with proven and potential therapeutic applications. However, most activities assayed in venoms (or their components) are of hemorrhagic, hypotensive, edematogenic, neurotoxic or myotoxic natures. Thus, other relevant activities might remain unknown. Using functional genomics coupled to the connectivity map (C-map) approach, we undertook a wide range indirect search for biological activities within the venom of the South American pit viper Bothrops jararaca . For that effect, venom was incubated with human breast adenocarcinoma cell line (MCF7) followed by RNA extraction and gene expression analysis. A list of 90 differentially expressed genes was submitted to biosimilar drug discovery based on pattern recognition. Among the 100 highest-ranked positively correlated drugs, only the antihypertensive, antimicrobial (both antibiotic and antiparasitic), and antitumor classes had been previously reported for B. jararaca venom. The majority of drug classes identified were related to (1) antimicrobial activity; (2) treatment of neuropsychiatric illnesses (Parkinson’s disease, schizophrenia, depression, and epilepsy); (3) treatment of cardiovascular diseases, and (4) anti-inflammatory action. The C-map results also indicated that B. jararaca venom may have components that target G-protein-coupled receptors (muscarinic, serotonergic, histaminergic, dopaminergic, GABA, and adrenergic) and ion channels. Although validation experiments are still necessary, the C-map correlation to drugs with activities previously linked to snake venoms supports the efficacy of this strategy as a broad-spectrum approach for biological activity screening, and rekindles the snake venom-based search for new therapeutic agents.
机译:蛇毒是具有成熟和潜在治疗应用的分子来源。然而,在毒液(或其成分)中测定的大多数活性具有出血,降压,水肿,神经毒性或肌毒性性质。因此,其他相关活动可能仍然未知。使用功能基因组学和连通性图(C-map)方法,我们对南美蛇毒蛇Bothrops jararaca的毒液内的生物活性进行了广泛的间接搜索。为此,将毒液与人乳腺癌细胞系(MCF7)孵育,然后进行RNA提取和基因表达分析。基于模式识别,将90种差异表达基因的列表提交给生物仿制药发现。在100种排名最高的正相关药物中,以前仅报道过Jararaca毒液的降压药,抗微生物药(包括抗生素和抗寄生虫药)和抗肿瘤药。确定的大多数药物类别与(1)抗菌活性有关; (2)神经精神疾病(帕金森氏症,精神分裂症,抑郁症和癫痫病)的治疗; (3)治疗心血管疾病,以及(4)抗炎作用。 C-map结果还表明,jararaca毒液可能具有靶向G蛋白偶联受体(毒蕈碱,血清素,组胺,多巴胺,GABA和肾上腺素)和离子通道的成分。尽管仍然需要进行验证实验,但与先前与蛇毒有关的具有活性的药物的C-map相关性支持该策略作为生物活性筛选的广谱方法的有效性,并重新激发了基于蛇毒的新治疗剂的搜索。

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