» Articles » PMID: 33143088

Protective Role of St. John's Wort and Its Components Hyperforin and Hypericin Against Diabetes Through Inhibition of Inflammatory Signaling: Evidence from In Vitro and In Vivo Studies

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2020 Nov 4
PMID 33143088
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Diabetes mellitus is a very common chronic disease with progressively increasing prevalence. Besides the well-known autoimmune and inflammatory pathogenesis of type 1 diabetes, in many people, metabolic changes and inappropriate lifestyle favor a subtle chronic inflammatory state that contributes to development of insulin resistance and progressive loss of β-cell function and mass, eventually resulting in metabolic syndrome or overt type 2 diabetes. In this paper, we review the anti-inflammatory effects of the extract of L. (St. John's wort, SJW) and its main active ingredients firstly in representative pathological situations on inflammatory basis and then in pancreatic β cells and in obese or diabetic animal models. The simultaneous and long-lasting inhibition of signal transducer and activator of transcription (STAT)-1, nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) and mitogen-activated protein kinases (MAPKs)/c-jun N-terminal kinase (JNK) signaling pathways involved in pro-inflammatory cytokine-induced β-cell dysfunction/death and insulin resistance make SJW particularly suitable for both preventive and therapeutic use in metabolic diseases. Hindrance of inflammatory cytokine signaling is likely dependent on the hyperforin content of SJW extract, but recent data reveal that hypericin can also exert relevant protective effects, mediated by activation of the cyclic adenosine monophosphate (cAMP)/protein kinase cAMP-dependent (PKA)/adenosine monophosphate activated protein kinase (AMPK) pathway, against high-fat-diet-induced metabolic abnormalities. Actually, the mechanisms of action of the two main components of SJW appear complementary, strengthening the efficacy of the plant extract. Careful quantitative analysis of SJW components and suitable dosage, with monitoring of possible drug-drug interaction in a context of remarkable tolerability, are easily achievable pre-requisites for forthcoming clinical applications.

Citing Articles

Tocotrienols in Different Parts of Wild L. Populations in Poland.

Gornas P, Symoniuk E Molecules. 2025; 30(5).

PMID: 40076360 PMC: 11902190. DOI: 10.3390/molecules30051137.


The Putative Antidiabetic Effect of on Diabetes Mellitus.

Theodorakopoulou A, Pylarinou I, Anastasiou I, Tentolouris N Int J Mol Sci. 2025; 26(1.

PMID: 39796209 PMC: 11719930. DOI: 10.3390/ijms26010354.


Preventive effect of hyperforin on lipopolysaccharide-induced acute kidney injury and inflammation by repressing the NF-κB/miR-21 axis.

Fan H, He X, Tong H, Chen K Cent Eur J Immunol. 2024; 49(2):169-186.

PMID: 39381550 PMC: 11457569. DOI: 10.5114/ceji.2024.140636.


Dermal Delivery of (L.) Loaded Nanogel: Formulation to Preclinical Psoriasis Assessment.

Singh N, Yadav S, Gupta P, Ali F, Arora S Recent Adv Drug Deliv Formul. 2024; 18(2):138-154.

PMID: 38808393 DOI: 10.2174/0126673878288239240415041832.


Hyperforin modulates MAPK/CCL11 signaling to reduce the inflammatory response of nasal mucosal epithelial cells caused by allergic rhinitis by targeting BCL6.

Xu C, Su W Exp Ther Med. 2023; 26(6):579.

PMID: 38023351 PMC: 10655049. DOI: 10.3892/etm.2023.12278.


References
1.
Iqbal M, Ho H, Petropoulos S, Moisiadis V, Gibb W, Matthews S . Pro-inflammatory cytokine regulation of P-glycoprotein in the developing blood-brain barrier. PLoS One. 2012; 7(8):e43022. PMC: 3433182. DOI: 10.1371/journal.pone.0043022. View

2.
Khan H, Sureda A, Belwal T, Cetinkaya S, Suntar I, Tejada S . Polyphenols in the treatment of autoimmune diseases. Autoimmun Rev. 2019; 18(7):647-657. PMC: 6588481. DOI: 10.1016/j.autrev.2019.05.001. View

3.
Di Paola R, Mazzon E, Muia C, Crisafulli C, Genovese T, Di Bella P . Protective effect of Hypericum perforatum in zymosan-induced multiple organ dysfunction syndrome: relationship to its inhibitory effect on nitric oxide production and its peroxynitrite scavenging activity. Nitric Oxide. 2006; 16(1):118-30. DOI: 10.1016/j.niox.2006.05.006. View

4.
Han M, Jung D, Morel C, Lakhani S, Kim J, Flavell R . JNK expression by macrophages promotes obesity-induced insulin resistance and inflammation. Science. 2012; 339(6116):218-22. PMC: 3835653. DOI: 10.1126/science.1227568. View

5.
Gunes S, Tamburaci S, Tihminlioglu F . A novel bilayer zein/MMT nanocomposite incorporated with H. perforatum oil for wound healing. J Mater Sci Mater Med. 2019; 31(1):7. DOI: 10.1007/s10856-019-6332-9. View