Thứ Bảy, 29 tháng 3, 2025

Rượu bia không chỉ ảnh hưởng đến gan mà còn gây viêm nướu, trào ngược axit, viêm tụy mãn tính và ung thư chết người. Uống quá nhiều rượu là kẻ hủy hoại thầm lặng sức khỏe đường tiêu hóa, tàn phá toàn bộ hệ tiêu hóa.

 







New Research Reveals the Effects of Alcohol on the Entire Digestive System

lcohol doesn’t just impact the liver, it wreaks havoc on the entire digestive system. From inflamed gums and acid reflux to chronic pancreatitis and deadly cancers, excessive drinking is a silent destroyer of gastrointestinal health.

The liver, responsible for breaking down alcohol, suffers immense damage, leading to cirrhosis and even liver cancer. Meanwhile, the stomach and intestines experience erosion, ulcers, and nutrient malabsorption. The pancreas is at risk for life-threatening pancreatitis, while the gallbladder can develop painful gallstones. Even more alarming, alcohol significantly raises the risk of deadly gastrointestinal cancers. Reducing alcohol intake is the best way to protect digestive health and prevent irreversible damage.

The Hidden Toll of Alcohol on Digestive Health

Excessive alcohol consumption is a major public health issue, contributing to 6% of all deaths worldwide and 5.1% of the global disease burden. It is a key risk factor for more than 200 diseases, including liver cirrhosis, pancreatitis, and esophageal cancer, with particularly severe effects on the digestive system. More than half of alcohol-related deaths are linked to gastrointestinal diseases, underscoring the need to understand how alcohol affects digestion. This review explores how the body processes ethanol and how alcohol consumption contributes to diseases affecting the liver, gastrointestinal tract, pancreas, and gallbladder.

Liver

The liver is the primary site of alcohol metabolism, processing about 90% of the alcohol a person consumes. Once inside the liver, ethanol is broken down into acetaldehyde by the enzyme alcohol dehydrogenase (ADH). Acetaldehyde, a highly toxic substance, is then converted into acetate, which eventually breaks down into carbon dioxide and water.

However, acetaldehyde can cause significant damage to liver cells, leading to a range of liver diseases. These include fatty liver (steatosis), liver inflammation (steatohepatitis and alcoholic hepatitis), scarring (fibrosis and cirrhosis), and even liver cancer (hepatocellular carcinoma or HCC). Chronic alcohol use speeds up liver damage, and factors such as genetics and the type of alcohol consumed can influence disease progression. Women are particularly vulnerable to alcohol-related liver damage due to differences in metabolism and body composition, making them more susceptible to long-term harm.

Gastrointestinal Tract

The gastrointestinal tract is often the first to show damage from excessive alcohol consumption, which can cause both reversible and irreversible lesions. Alcohol can lead to stomatitis, periodontal disease, and alterations in the oral microbiota. In the esophagus, alcohol’s toxic effects contribute to esophagitis, gastroesophageal reflux disease, and an increased risk of esophageal cancer, particularly when combined with smoking.

Alcohol also affects gastric motility and mucosal integrity, contributing to conditions like gastritis, peptic ulcers, and eventually gastric cancer. Chronic alcohol use can impair intestinal barrier function, leading to “leaky gut,” dysbiosis, and nutrient malabsorption. These changes increase the risk of diarrhea and contribute to colorectal cancer development.

Pancreas

Alcohol misuse is a leading cause of pancreatitis. Acute pancreatitis (AP) and chronic pancreatitis are common consequences of alcohol consumption. In AP, excessive alcohol intake leads to inflammation and pancreatic tissue damage, while chronic pancreatitis involves persistent inflammation, fibrosis, and pancreatic insufficiency.

The pathophysiology of alcohol-induced pancreatitis is multifactorial, involving both direct toxic effects on pancreatic cells and indirect effects through the activation of inflammatory and fibrotic pathways. Pancreatic cancer is also a severe consequence of long-term alcohol abuse, with alcohol serving as a cofactor in the disease’s development, particularly when combined with smoking.

Gallbladder

Alcohol consumption is associated with an increased risk of gallstones and gallbladder disease. Alcohol can alter bile composition, contributing to the formation of gallstones, and chronic alcohol use can lead to gallbladder inflammation, resulting in conditions like cholecystitis. Additionally, alcohol abuse can exacerbate pre-existing gallbladder issues by increasing oxidative stress and promoting the secretion of inflammatory cytokines.

Gastrointestinal Tumors

Alcohol is a significant risk factor for various gastrointestinal cancers, particularly those in the esophagus, stomach, and colon. Ethanol metabolism produces acetaldehyde, a potent carcinogen that can damage DNA, inhibit DNA repair, and shorten telomeres, contributing to carcinogenesis. Alcohol consumption, particularly in combination with smoking, significantly increases the risk of esophageal squamous cell carcinoma and gastric cancer. It is also associated with an elevated risk of colorectal cancer through mechanisms like DNA methylation induced by alcohol.

Discussion

Chronic alcohol consumption results in a broad spectrum of damage across the digestive system, from the oral cavity to the rectum. The severity of the damage depends on factors such as the amount and frequency of alcohol intake, genetic predisposition, and the presence of other risk factors. The interaction of alcohol with other drugs, particularly in women, can further exacerbate its harmful effects. Acetaldehyde and endotoxemia triggered by alcohol intake play critical roles in liver damage, leading to conditions like cirrhosis and liver cancer. Early detection and management of alcohol-induced damage are essential to prevent progression to more severe conditions like pancreatitis, cirrhosis, and cancer.

Conclusions

Minimizing alcohol intake is crucial for digestive health. Social drinking, defined as up to one drink per day for women and two drinks per day for men, is considered the safest approach. Individuals with alcohol use disorder should seek professional support and management to reduce the risk of gastrointestinal damage. Immediate medical evaluation is recommended for patients who present with persistent digestive symptoms linked to excessive alcohol consumption.

Reference: “Effects of Ethanol on the Digestive System: A Narrative Review” by Fabio Caputo, Matteo Guarino, Alberto Casabianca, Lisa Lungaro, Anna Costanzini, Giacomo Caio, Giorgio Zoli and Roberto De Giorgio, 2024, Journal of Translational Gastroenterology.
DOI: 10.14218/JTG.2024.00028

Thứ Sáu, 21 tháng 3, 2025

Nghiên cứu mới liên hệ giữa mỡ bụng và sức khỏe não bộ

 Nghiên cứu mới liên hệ giữa mỡ bụng và sức khỏe não bộ, 





Mô mỡ nội tạng hỗ trợ duy trì mức yếu tố dinh dưỡng thần kinh có nguồn gốc từ não (BDNF) trong não. Tác động của mô mỡ nội tạng lên biểu hiện BDNF của não giảm dần theo tuổi tác.

Một số cơ chế tương ứng với việc tăng cân ở tuổi trung niên dường như có liên quan đến quá trình lão hóa não.  

Những phát hiện này có thể góp phần ngăn ngừa và cải thiện tình trạng suy giảm nhận thức và các triệu chứng trầm cảm ở người lớn tuổi.

New research reveals that visceral adipose tissue helps maintain brain-derived neurotrophic factor (BDNF) levels, but this effect weakens with age, potentially contributing to cognitive decline.

A new study, led by Dr. Yoshinori Takei and Dr. Atsushi Sugiyama from Toho University’s Department of Pharmacology, along with Dr. Akira Hirasawa of Kyoto University’s Graduate School of Pharmaceutical Sciences and Dr. Yoko Amagase of Osaka Medical and Pharmaceutical University’s Faculty of Pharmacy, uncovers a novel link between visceral adipose tissue aging and brain health.

The findings were recently published in GeroScience, the official journal of the American Aging Association.

Key Points

  • Visceral adipose tissue aids in maintaining the brain-derived neurotrophic factor (BDNF) level in the brain.
  • The effects of the visceral adipose tissue on brain BDNF expression decrease with age.
  • Some mechanisms corresponding to middle-aged weight gain appear to be involved in brain aging.
  • The findings may contribute to the prevention and improvement of cognitive decline and depressive symptoms in older adults.

https://scitechdaily.com/new-study-links-belly-fat-and-brain-health-a-key-to-preventing-cognitive-decline/