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导致血管收缩和心肌抑制的 elusive 毒素:对 cleistanthoside A 的详细核磁共振分析和生物学研究。 (注:“elusive”直译为“难以捉摸的”,这里结合语境推测可能是一种特定毒素名称,暂保留英文未翻译)

Elusive Toxin in Causing Vasoconstriction and Myocardial Depression: Detailed NMR Analyses and Biological Studies of Cleistanthoside A.

作者信息

Amirtham Soosai Manickam, Prince Neetu, Venkateswarulu Mangili, Chandra Mondal Iswar, Raman Swetha, Raj Renu, Rajendran Elanchezhian, Jebaraj Benjamin, Vaithiyalingam Abirami, Rajasegaran Rajalakshmi, Mukadam Farhan Adam, Bhaskar Anand, Ghosh Subrata, Conrad Jürgen, Beifuss Uwe, Subramani Sathya

机构信息

Department of Physiology, Christian Medical College, Thorapadi post, Vellore, 632002 Tamilnadu, India.

School of Basic Sciences, Indian Institute of Technology, Mandi, 175005 Himachal Pradesh, India.

出版信息

ACS Omega. 2021 Sep 13;6(38):24553-24561. doi: 10.1021/acsomega.1c03138. eCollection 2021 Sep 28.

Abstract

leaf extracts are consumed for suicidal purposes in southern India. The boiled decoction is known to be more toxic than the fresh leaf juice. Although several compounds have been isolated and their toxicity tested, controversy remains as to which compounds are responsible for the high level of toxicity of . We report herein that cleistanthoside A is the major toxin in the boiled aqueous extract of fresh leaves and causes death in rats in small doses. The toxicity of the boiled extract prepared in the manner described can be attributed entirely to cleistanthoside A. Cleistanthin A could also be isolated from the boiled extract, albeit in trace amounts. As hypotension not responding to vasoconstrictors is the cause of death in patients who have consumed the boiled extract, effects of cleistanthoside A on the determinants of blood pressure, namely, force of cardiac contraction and vascular resistance, were tested in isolated organ experiments. Cleistanthoside A has a direct vasoconstrictor effect; however, it inhibits ventricular contractility. Therefore, the notion that the shock in poisoning is of vascular origin must be considered carefully, and the possibility of cardiogenic shock must be studied. We present the crystal structure of cleistanthin A and show the potency of fast NMR methods (NOAH4-BSCN-NUS) in the full spectral assignment of cleistanthoside A as a real-world sample of a natural product. We also compare the results of the NOAH4-BSCN-NUS NMR experiments with conventional NMR methods.

摘要

在印度南部,有人会出于自杀目的食用树叶提取物。已知煮沸后的煎剂比新鲜树叶汁毒性更强。尽管已经分离出了几种化合物并测试了它们的毒性,但对于哪种化合物导致了[树叶提取物]的高毒性仍存在争议。我们在此报告,cleistanthoside A是新鲜树叶煮沸水提取物中的主要毒素,小剂量就能导致大鼠死亡。以所述方式制备的煮沸提取物的毒性可完全归因于cleistanthoside A。虽然也能从煮沸提取物中分离出痕量的Cleistanthin A,但含量极少。由于食用煮沸提取物的患者死亡原因是对血管收缩剂无反应的低血压,因此在离体器官实验中测试了cleistanthoside A对血压决定因素(即心脏收缩力和血管阻力)的影响。Cleistanthoside A具有直接的血管收缩作用;然而,它会抑制心室收缩力。因此,必须仔细考虑[该树叶提取物]中毒导致的休克是血管源性的这一观点,并且必须研究心源性休克的可能性。我们展示了Cleistanthin A的晶体结构,并展示了快速核磁共振方法(NOAH4 - BSCN - NUS)在对cleistanthoside A进行全谱归属时作为天然产物实际样品的效能。我们还将NOAH4 - BSCN - NUS核磁共振实验的结果与传统核磁共振方法的结果进行了比较。

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