Bulfone Tommaso C, Samuel Stephen P, Bickler Philip E, Lewin Matthew R
California Academy of Sciences, San Francisco, 94118 CA, USA.
Ophirex, Inc., Corte Madera, 94925 CA, USA.
J Trop Med. 2018 Jul 30;2018:4320175. doi: 10.1155/2018/4320175. eCollection 2018.
The World Health Organization (WHO) recently added snakebite envenoming to the priority list of Neglected Tropical Diseases (NTD). It is thought that ~75% of mortality following snakebite occurs outside the hospital setting, making the temporal gap between a bite and antivenom administration a major therapeutic challenge. Small molecule therapeutics (SMTs) have been proposed as potential prereferral treatments for snakebite to help address this gap. Herein, we discuss the characteristics, potential uses, and development of SMTs as potential treatments for snakebite envenomation. We focus on SMTs that are secretory phospholipase A2 (sPLA) inhibitors with brief exploration of other potential drug targets on venom molecules.
世界卫生组织(WHO)最近将蛇咬伤中毒列入被忽视热带病(NTD)的优先事项清单。据认为,蛇咬伤后的死亡率约75%发生在医院环境之外,这使得咬伤与抗蛇毒血清给药之间的时间间隔成为一个重大的治疗挑战。小分子疗法(SMTs)已被提议作为蛇咬伤的潜在院前治疗方法,以帮助解决这一间隔问题。在此,我们讨论SMTs作为蛇咬伤中毒潜在治疗方法的特性、潜在用途和开发情况。我们重点关注作为分泌型磷脂酶A2(sPLA)抑制剂的SMTs,并简要探讨毒液分子上的其他潜在药物靶点。