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重新审视矛头蝮蛇毒液的治疗潜力:利用连通性映射筛选新的活性。

Revisiting the Therapeutic Potential of Bothrops jararaca Venom: Screening for Novel Activities Using Connectivity Mapping.

机构信息

Laboratory of Toxinology, Oswaldo Cruz Institute, FIOCRUZ, Rio de Janeiro, RJ 21040-900, Brazil.

National Institute of Science and Technology on Toxins (INCTTOX), CNPq, Brasília, DF 71605-170, Brazil.

出版信息

Toxins (Basel). 2018 Feb 6;10(2):69. doi: 10.3390/toxins10020069.

Abstract

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 . 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 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 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.

摘要

蛇毒是具有已证实和潜在治疗应用的分子的来源。然而,在毒液(或其成分)中测定的大多数活性都是出血性、降压性、水肿性、神经毒性或肌毒性。因此,其他相关的活性可能仍然未知。我们使用功能基因组学结合连接图谱(C-map)方法,对南美响尾蛇毒液中的生物活性进行了广泛的间接搜索。为此,将毒液与人类乳腺腺癌细胞系(MCF7)孵育,然后提取 RNA 并进行基因表达分析。将 90 个差异表达基因列表提交给基于模式识别的生物相似药物发现。在 100 种相关性最高的正相关药物中,只有降压药、抗菌药(抗生素和抗寄生虫药)和抗肿瘤药类先前被报道过与 毒液有关。确定的大多数药物类别与(1)抗菌活性;(2)治疗神经精神疾病(帕金森病、精神分裂症、抑郁症和癫痫);(3)治疗心血管疾病;(4)抗炎作用有关。C-map 结果还表明, 毒液可能含有针对 G 蛋白偶联受体(毒蕈碱、血清素能、组氨酸能、多巴胺能、GABA 和肾上腺素能)和离子通道的成分。尽管验证实验仍然是必要的,但 C-map 与先前与蛇毒相关的具有活性的药物的相关性支持了该策略作为广谱生物活性筛选方法的有效性,并重新点燃了基于蛇毒寻找新治疗剂的搜索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d26/5848170/cebf056fc5db/toxins-10-00069-g001.jpg

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