» Articles » PMID: 29118341

Novel Serotonin Transporter Regulators: Natural Aristolane- and Nardosinane- Types of Sesquiterpenoids from Nardostachys Chinensis Batal

Overview
Journal Sci Rep
Specialty Science
Date 2017 Nov 10
PMID 29118341
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Serotonin transporter (SERT) is a classic target of drug discovery for neuropsychiatric and digestive disorders, and against those disorders, plants of Nardostachys genus have been valued for centuries in the systems of Traditional Chinese Medicine, Ayurvedic and Unani. Herein, chemical investigation on the roots and rhizomes of Nardostachys chinensis Batal. led to the isolation of forty sesquiterpenoids including six new aristolane-type sesquiterpenoids and six new nardosinane-type sesquiterprenoids. Their structures were elucidated by extensive spectroscopic methods, combined with analyses of circular dichroism and single-crystal X-ray diffraction data. To explore natural product scaffolds with SERT regulating activity, a high-content assay for measurement of SERT function in vitro was conducted to evaluate the SERT regulating properties of these isolates. In conclusion, eleven compounds could be potential natural product scaffolds for developing drug candidates targeting SERT. Among which, kanshone C of aristolane-type sesquiterpenoid inhibited SERT most strongly, while desoxo-nachinol A of nardosinane-type sesquiterpenoid instead enhanced SERT potently.

Citing Articles

Natural Occurring Terpene Cyclic Anhydrides: Biosynthetic Origin and Biological Activities.

Molina Inzunza D, Martin Gonzalez J, Segura Navarro M, Barrero A, Quilez Del Moral J Biomolecules. 2024; 14(8).

PMID: 39199343 PMC: 11352521. DOI: 10.3390/biom14080955.


Research Progress on Sesquiterpene Compounds from Artabotrys Plants of Annonaceae.

Sun Y, Xin J, Xu Y, Wang X, Zhao F, Niu C Molecules. 2024; 29(7).

PMID: 38611927 PMC: 11013193. DOI: 10.3390/molecules29071648.


Degradation Profiling of Nardosinone at High Temperature and in Simulated Gastric and Intestinal Fluids.

Xue B, Yang T, He R, Gao W, Lai J, Liu S Molecules. 2023; 28(14).

PMID: 37513256 PMC: 10385092. DOI: 10.3390/molecules28145382.


Structures, Occurrences and Biosynthesis of 11,12,13-Tri--Sesquiterpenes, an Intriguing Class of Bioactive Metabolites.

Coca-Ruiz V, Suarez I, Aleu J, Collado I Plants (Basel). 2022; 11(6).

PMID: 35336651 PMC: 8949605. DOI: 10.3390/plants11060769.


Chemical Analysis of the Ingredients of 20% Aqueous Ethanol Extract of through Phytochemical Study and Evaluation of Anti-Neuroinflammatory Component.

Kim K, Yoon C, Park S, Bae G, Kim D, Kim Y Evid Based Complement Alternat Med. 2021; 2021:5901653.

PMID: 33976703 PMC: 8084687. DOI: 10.1155/2021/5901653.


References
1.
Bismuth-Evenzal Y, Roz N, Gurwitz D, Rehavi M . N-methyl-citalopram: A quaternary selective serotonin reuptake inhibitor. Biochem Pharmacol. 2010; 80(10):1546-52. DOI: 10.1016/j.bcp.2010.07.035. View

2.
Chen J, Pan H, Rothman T, Wade P, Gershon M . Guinea pig 5-HT transporter: cloning, expression, distribution, and function in intestinal sensory reception. Am J Physiol. 1998; 275(3):G433-48. DOI: 10.1152/ajpgi.1998.275.3.G433. View

3.
Roggen H, Kehler J, Stensbol T, Hansen T . Synthesis of enantiomerically pure milnacipran analogs and inhibition of dopamine, serotonin, and norepinephrine transporters. Bioorg Med Chem Lett. 2007; 17(10):2834-7. DOI: 10.1016/j.bmcl.2007.02.054. View

4.
Zhang A, Zhou G, Johnson K, Zhang M, Kozikowski A . Thiophene derivatives: a new series of potent norepinephrine and serotonin reuptake inhibitors. Bioorg Med Chem Lett. 2002; 12(7):993-5. DOI: 10.1016/s0960-894x(02)00103-8. View

5.
Soubhye J, Aldib I, Prevost M, Elfving B, Gelbcke M, Podrecca M . Hybrid molecules inhibiting myeloperoxidase activity and serotonin reuptake: a possible new approach of major depressive disorders with inflammatory syndrome. J Pharm Pharmacol. 2014; 66(8):1122-32. DOI: 10.1111/jphp.12236. View