Insights into the Cardiotoxic Effects of Veratrum Lobelianum Alkaloids: Pilot Study.
Amir TaldaevRoman P TerekhovElizaveta V MelnikMaria V BelovaSergey V KozinAndrey Anatolevich NedorubovTatyana Ya PomerantsevaGalina V RamenskayaPublished in: Toxins (2022)
Jervine, protoveratrine A (proA), and protoveratrine B (proB) are Veratrum alkaloids that are presented in some remedies obtained from Veratrum lobelianum , such as Veratrum aqua . This paper reports on a single-center pilot cardiotoxic mechanism study of jervine, proA, and proB in case series. The molecular aspects were studied via molecular dynamic simulation, molecular docking with cardiac sodium channel Na V 1.5, and machine learning-based structure-activity relationship modeling. HPLC-MS/MS method in combination with clinical events were used to analyze Veratrum alkaloid cardiotoxicity in patients. Jervine demonstrates the highest docking score (-10.8 kcal/mol), logP value (4.188), and p K a value (9.64) compared with proA and proB. Also, this compound is characterized by the lowest calculated IC 50 . In general, all three analyzed alkaloids show the affinity to Na V 1.5 that highly likely results in cardiotoxic action. The clinical data of seven cases of intoxication by Veratrum aqua confirms the results of molecular modeling. Patients exhibited nausea, muscle weakness, bradycardia, and arterial hypotension. The association between alkaloid concentrations in blood and urine and severity of patient condition is described. These experiments, while primary, confirmed that jervine, proA, and proB contribute to cardiotoxicity by Na V 1.5 inhibition.
Keyphrases
- ms ms
- end stage renal disease
- molecular docking
- machine learning
- ejection fraction
- newly diagnosed
- peritoneal dialysis
- prognostic factors
- randomized controlled trial
- left ventricular
- molecular dynamics simulations
- mass spectrometry
- small molecule
- deep learning
- skeletal muscle
- artificial intelligence
- electronic health record
- molecular dynamics
- simultaneous determination
- protein protein