Network pharmacology and molecular docking reveal potential mechanisms of ginseng in the treatment of diabetes mellitus-induced erectile dysfunction and asthenospermia

Author:

Liu Liming12,Zhang Yuanfeng34,Yang Jiashu2,Chen Wenfang5,Lan Kaijian4,Shi Yibo3,Zhang Xiaogang6,Xing Xiping7ORCID

Affiliation:

1. Department of Andrology, Xi’an Hospital of Traditional Chinese Medicine,Xi’an, P. R. China

2. School of Integrated Chinese and Western Medicine, Gansu University of Chinese Medicine, Lanzhou, P. R. China

3. Department of Urology, Key Laboratory of Urological Disease of Gansu Province, Clinical Center of Gansu Province for Nephron-Urology, Lanzhou University Second Hospital, Lanzhou, P. R. China

4. Department of Urology, Shantou Central Hospital, Shantou, P. R. China

5. The Second Clinical Medical College, Lanzhou University, Lanzhou, P. R. China

6. Department of Cardiology, Affiliated Hospital of Gansu Medical College, Pingliang, P. R. China

7. Department of Urology and Andrology, Affiliated Hospital of Gansu University of Chinese Medicine, Lanzhou, P. R. China.

Abstract

Diabetes mellitus (DM) is a chronic metabolic disease that predisposes to chronic damage and dysfunction of various organs, including leading to erectile dysfunction (ED) and asthenospermia. Literature suggests that ginseng plays an important role in the treatment and management of DM. Ginseng may have a therapeutic effect on the complications of DM-induced ED and asthenospermia. The study aimed to explore the mechanisms of ginseng in the treatment of DM-induced ED and asthenospermia following the Traditional Chinese Medicine (TCM) theory of “treating different diseases with the same treatment.” This study used network pharmacology and molecular docking to examine the potential targets and pharmacological mechanism of Ginseng for the treatment of DM-induced ED and asthenospermia. The chemical ingredients and targets of ginseng were acquired using the Traditional Chinese Medicine Systems Pharmacology database and analysis platform. The targets of DM, ED, and asthenospermia were extracted with the GeneCards and Online Mendelian Inheritance in Man databases. A protein–protein interaction network analysis was constructed. The Metascape platform was applied for analyzing the gene ontology and Kyoto Encyclopedia of Genes and Genomes pathways. AutoDock Vina was used to perform molecular docking. Network pharmacology revealed that the main active components of the target of action were kaempferol, beta-sitosterol, ginsenoside rh2, stigmasterol, and fumarine. Core targets of the protein–protein interaction network included TNF, IL-1β, AKT1, PTGS2, BCL2, and JUN. Kyoto Encyclopedia of Genes and Genomes enrichment analysis showed that they were mainly involved in AGE-RAGE signaling pathway in diabetic complications, TNF signaling pathway, Lipid and atherosclerosis. The interactions of core active components and targets were analyzed by molecular docking. Ginseng may play a comprehensive therapeutic role in the treatment of DM-induced ED and asthenospermia through “multicomponent, multi-target, and multi-pathway” biological mechanisms such as inflammation and oxidative stress.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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