Probiotics isolated from the fermented grains of Chinese baijiu alleviates alcohol-induced liver injury by regulating alcohol metabolism and gut microbiota in mice DOI
Jiali Wang,

Qiang Xu,

Chengshun Lu

et al.

Food & Function, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 1, 2025

Probiotics isolated from the fermented grains of Chinese baijiu can prevent drunkenness, aid sobriety, protect against chronic alcoholic liver injury, and modulate intestinal flora imbalance short-chain fatty acids in affected mice.

Language: Английский

CYP2E1 in Alcoholic and Non-Alcoholic Liver Injury. Roles of ROS, Reactive Intermediates and Lipid Overload DOI Open Access
Riina Harjumäki, Chris S. Pridgeon, Magnus Ingelman‐Sundberg

et al.

International Journal of Molecular Sciences, Journal Year: 2021, Volume and Issue: 22(15), P. 8221 - 8221

Published: July 30, 2021

CYP2E1 is one of the fifty-seven cytochrome P450 genes in human genome and highly conserved. a unique enzyme because its heme iron constitutively high spin state, allowing direct reduction of, e.g., dioxygen, causing formation variety reactive oxygen species xenobiotics to toxic products. The has been focus scientific interest due (i) important endogenous function liver homeostasis, (ii) ability activate procarcinogens convert certain drugs, paracetamol anesthetics, cytotoxic end products, (iii) effectively reduce dioxygen radical injury, (iv) capability compounds, often generating intermediates or indirect immunotoxic properties (v) contribution development alcoholic disease, steatosis NASH. In this overview, we present discovery studies humans, 3D systems genetically modified mice disclose clinical relevance. Induction either by alcohol high-fat diet leads increased severity pathology likelihood develop ALD NASH, with subsequent influence on occurrence hepatocellular cancer. Thus, fat-dependent induction might provide link between fibrosis liver. We conclude that many physiological functions key for hepatic carcinogenesis, drug toxicity disease.

Language: Английский

Citations

153

Gut dysbiosis, defective autophagy and altered immune responses in neurodegenerative diseases: Tales of a vicious cycle DOI
Saravana Babu Chidambaram, Musthafa Mohamed Essa,

Annan Gopinath Rathipriya

et al.

Pharmacology & Therapeutics, Journal Year: 2021, Volume and Issue: 231, P. 107988 - 107988

Published: Sept. 16, 2021

Language: Английский

Citations

124

The Influence of Gut Dysbiosis in the Pathogenesis and Management of Ischemic Stroke DOI Creative Commons
Saravana Babu Chidambaram,

Annan Gopinath Rathipriya,

Arehally M. Mahalakshmi

et al.

Cells, Journal Year: 2022, Volume and Issue: 11(7), P. 1239 - 1239

Published: April 6, 2022

Recent research on the gut microbiome has revealed influence of microbiota (GM) ischemic stroke pathogenesis and treatment outcomes. Alterations in diversity, abundance, functions microbiome, termed dysbiosis, results dysregulated gut–brain signaling, which induces intestinal barrier changes, endotoxemia, systemic inflammation, infection, affecting post-stroke Gut–brain interactions are bidirectional, signals from to brain mediated by microbially derived metabolites, such as trimethylamine N-oxide (TMAO) short-chain fatty acids (SCFAs); bacterial components, lipopolysaccharide (LPS); immune cells, T helper cells; translocation via hormonal, immune, neural pathways. Ischemic affects microbial composition hypothalamic–pituitary–adrenal (HPA) pathways, can contribute Experimental clinical studies have demonstrated that restoration usually improves outcomes regulating metabolic, inflammatory responses axis (GBA). Therefore, restoring healthy ecology may be a key therapeutic target for effective management stroke.

Language: Английский

Citations

111

Mechanistic Insights into the Link between Gut Dysbiosis and Major Depression: An Extensive Review DOI Creative Commons

Sharma Sonali,

Bipul Ray,

Hediyal Ahmed Tousif

et al.

Cells, Journal Year: 2022, Volume and Issue: 11(8), P. 1362 - 1362

Published: April 16, 2022

Depression is a highly common mental disorder, which often multifactorial with sex, genetic, environmental, and/or psychological causes. Recent advancements in biomedical research have demonstrated clear correlation between gut dysbiosis (GD) or microbial and the development of anxiety depressive behaviors. The microbiome communicates brain through neural, immune, metabolic pathways, either directly (via vagal nerves) indirectly gut- microbial-derived metabolites as well hormones endocrine peptides, including peptide YY, pancreatic polypeptide, neuropeptide Y, cholecystokinin, corticotropin-releasing factor, glucagon-like peptide, oxytocin, ghrelin). Maintaining healthy microbiota (GM) now being recognized important for health use probiotics, prebiotics, synbiotics, fecal transplantation (FMT), etc. A few approaches exert antidepressant effects via restoring GM hypothalamus–pituitary–adrenal (HPA) axis functions. In this review, we summarized etiopathogenic link depression preclinical clinical evidence. addition, collated information on recent therapies supplements, such short-chain fatty acids, vitamin B12, omega-3 etc., target gut–brain (GBA) effective management behavior anxiety.

Language: Английский

Citations

106

Contributing roles of mitochondrial dysfunction and hepatocyte apoptosis in liver diseases through oxidative stress, post-translational modifications, inflammation, and intestinal barrier dysfunction DOI Creative Commons
Karli R. LeFort, Wiramon Rungratanawanich, Byoung‐Joon Song

et al.

Cellular and Molecular Life Sciences, Journal Year: 2024, Volume and Issue: 81(1)

Published: Jan. 12, 2024

Abstract This review provides an update on recent findings from basic, translational, and clinical studies the molecular mechanisms of mitochondrial dysfunction apoptosis hepatocytes in multiple liver diseases, including but not limited to alcohol-associated disease (ALD), metabolic dysfunction-associated steatotic (MASLD), drug-induced injury (DILI). While ethanol-inducible cytochrome P450-2E1 (CYP2E1) is mainly responsible for oxidizing binge alcohol via microsomal ethanol system, it also metabolizing many xenobiotics, pollutants, chemicals, drugs, specific diets abundant n-6 fatty acids, into toxic metabolites organs, liver, causing pathological insults through organelles such as mitochondria endoplasmic reticula. Oxidative imbalances (oxidative stress) promote covalent modifications lipids, proteins, nucleic acids enzymatic non-enzymatic mechanisms. Excessive changes stimulate various post-translational (PTMs) transcription factors, histones. Increased PTMs proteins inactivate enzymes involved reduction oxidative species, acid metabolism, mitophagy pathways, leading dysfunction, energy depletion, apoptosis. Unique other organelles, control signaling cascades bioenergetics (fat metabolism), inflammation, apoptosis/necrosis hepatocytes. When homeostasis shifted, these pathways become altered or shut down, likely contributing death with activation inflammation hepatic stellate cells, fibrosis cirrhosis. will encapsulate how contributes hepatocyte several types diseases order provide recommendations targeted therapeutics.

Language: Английский

Citations

45

Oxidative Stress, Gut Microbiota, and Extracellular Vesicles: Interconnected Pathways and Therapeutic Potentials DOI Open Access
Bo Ma, Muttiah Barathan, Min Hwei Ng

et al.

International Journal of Molecular Sciences, Journal Year: 2025, Volume and Issue: 26(7), P. 3148 - 3148

Published: March 28, 2025

Oxidative stress (OS) and gut microbiota are crucial factors influencing human health, each playing a significant role in the development progression of chronic diseases. This review provides comprehensive analysis complex interplay between these two factors, focusing on how an imbalance reactive oxygen species (ROS) antioxidants leads to OS, disrupting cellular homeostasis contributing range conditions, including metabolic disorders, cardiovascular diseases, neurological cancer. The microbiota, diverse community microorganisms residing gastrointestinal tract, is essential for regulating immune responses, pathways, overall health. Dysbiosis, composition, closely associated with inflammation, dysfunction, various highlights influences influenced by complicating pathophysiology many conditions. Furthermore, emerging evidence has identified extracellular vesicles (EVs) as critical facilitators crosstalk OS microbiota. EVs also play signaling host tissues, modulating processes. function holds promise targeted therapies aimed at restoring microbial balance mitigating OS. Personalized therapeutic approaches, probiotics, antioxidants, fecal transplantation-based strategies, can be used address OS-related diseases improve health outcomes. Nonetheless, further research needed study molecular mechanisms underlying interactions potential innovative interventions offer novel strategies managing enhancing

Language: Английский

Citations

2

Randomized Clinical Trial: Probiotics Alleviated Oral-Gut Microbiota Dysbiosis and Thyroid Hormone Withdrawal-Related Complications in Thyroid Cancer Patients Before Radioiodine Therapy Following Thyroidectomy DOI Creative Commons

Baiqiang Lin,

Fuya Zhao,

Yang Liu

et al.

Frontiers in Endocrinology, Journal Year: 2022, Volume and Issue: 13

Published: March 8, 2022

Background Thyroid hormone withdrawal (THW) in postoperative thyroid cancer patients who need always accompanied by complications (e.g., dyslipidemia and constipation). At present, there are no effective safe means to alleviate these complications. Purpose We aimed assess the oral-gut microbiota profiles THW then investigate whether probiotics could alleviating related therapeutic effects were associated with state. Methods Fifty eligible carcinoma undergoing thyroidectomy randomly assigned receive or placebo during THW. Complications assessed through validated questionnaires plasma lipid indicators. The complex preparation was composed of Bifidobacterium infantis , Lactobacillus acidophilus Enterococcus faecalis Bacillus cereus . Results Probiotics alleviated lack energy, constipation, weight gain, dry mouth decreased levels fecal/serum LPS indicators (total cholesterol, triglycerides, low-density lipoprotein, apolipoprotein A) (P < 0.05). Gut oral microbial diversity significantly after THW, while an increased dysbiosis index (MDI) observed. distinctly restored gut diversity. Increased Holdemanella Coprococcus_2 Fusobacterium Eubacterium_ruminantium_group Ruminococcus_1 Parasutterella found intervention. Lack seen be above microbiota. In addition, reduced Prevotella_9 Haemophilus Lautropia which positively correlated occurrence mouth. Conclusion reduce incidence may modifying Clinical Trial Registration [ https://clinicaltrials.gov/ ], identifier America Registry NCT03574051.

Language: Английский

Citations

37

ALDH2 deficiency increases susceptibility to binge alcohol-induced gut leakiness, endotoxemia, and acute liver injury in mice through the gut-liver axis DOI Creative Commons
Wiramon Rungratanawanich, Yuhong Lin, Xin Wang

et al.

Redox Biology, Journal Year: 2022, Volume and Issue: 59, P. 102577 - 102577

Published: Dec. 13, 2022

Mitochondrial aldehyde dehydrogenase 2 (ALDH2) is the major enzyme responsible for metabolizing toxic acetaldehyde to acetate and acts as a protective or defensive protein against various disease states associated with alcohol use disorder (AUD), including alcohol-related liver (ARLD). We hypothesized that Aldh2-knockout (KO) mice are more susceptible binge alcohol-mediated injury than wild-type (WT) through increased oxidative stress, gut leakiness endotoxemia. Therefore, this study aimed investigate role of ALDH2 in alcohol-induced permeability, endotoxemia, acute inflammatory by exposing Aldh2-KO WT single oral dose 3.5, 4.0, 5.0 g/kg. Our findings showed first time deficiency increases their sensitivity nitrative enterocyte apoptosis, nitration tight junction (TJ) adherent (AJ) proteins, leading degradation. These resulted endotoxemia after exposure ethanol even at 3.5 g/kg, while no changes were observed corresponding mice. The elevated serum endotoxin (lipopolysaccharide, LPS) bacterial translocation contributed systemic inflammation, hepatocyte subsequently gut-liver axis. Treatment Daidzin, an inhibitor, exacerbated ethanol-induced cell permeability reduced TJ/AJ proteins T84 human colon cells. reversed Alda-1, activator. Furthermore, CRISPR/Cas9-mediated knockout cells damage paracellular permeability. All these demonstrate critical epithelial barrier dysfunction suggest gene mutation humans risk factor injury, could be important therapeutic target alcohol-associated tissue organ damage.

Language: Английский

Citations

33

Antioxidant Materials in Oral and Maxillofacial Tissue Regeneration: A Narrative Review of the Literature DOI Creative Commons
Niloufar Abedi, Zahra Sadat Sajadi-Javan, Monireh Kouhi

et al.

Antioxidants, Journal Year: 2023, Volume and Issue: 12(3), P. 594 - 594

Published: Feb. 27, 2023

Oral and maxillofacial tissue defects caused by trauma, tumor reactions, congenital anomalies, ischemic diseases, infectious surgical resection, odontogenic cysts present a formidable challenge for reconstruction. Tissue regeneration using functional biomaterials cell therapy strategies has raised great concerns in the treatment of damaged during past few decades. However, implantation transplantation, production excessive reactive oxygen species (ROS) may hinder repair as it commonly causes severe injuries leading to damage. These products exist form oxidant molecules such hydrogen peroxide, superoxide ions, hydroxyl radicals, nitrogen oxide. days, many scientists have focused on application ROS-scavenging components body process. One these scavenging is antioxidants, which are beneficial materials tissues keeping safe against free radicals. Antioxidants divided into natural synthetic sources. In current review article, different antioxidant sources their mechanism action discussed. The applications antioxidants oral tissues, including hard cranial, alveolar bone, dental tissue, soft (dental pulp, periodontal tissue), facial nerve, cartilage also highlighted following parts.

Language: Английский

Citations

18

Rutin Trihydrate Conjugated Zinc Oxide Nanoparticles Targeting Oxidative Stress Pathways for the Protection of Gut Microbiome Dysfunction and Neurodegenerative Diseases DOI
Praveen Kumar Issac, Kadhirmathiyan Velumani

BioNanoScience, Journal Year: 2024, Volume and Issue: 14(5), P. 5310 - 5326

Published: May 10, 2024

Language: Английский

Citations

7