Triglyceride-Targeted Molecularly Imprinted Polymers Activate Lipophagy via Cargo Exchange for Nonalcoholic Fatty Liver Disease Treatment DOI

Yilin Wen,

Ping Weng,

Yueyue Li

и другие.

ACS Applied Polymer Materials, Год журнала: 2024, Номер 6(12), С. 7265 - 7277

Опубликована: Июнь 14, 2024

Lipid accumulation is a prominent pathologic feature of nonalcoholic fatty liver disease (NAFLD), which due to imbalances in triglycerides metabolism. However, none the available therapeutic strategies have been able achieve effective removal from lesion site. Herein, MIP@QUE, mimetic transporter with high affinity for triglycerides, was synthesized using molecular imprinting. The physicochemical features MIP@QUE are such that it binds and releases drug an affinity-driven reaction. In vivo vitro experiments showed metabolism promoted by dual activation autophagy-lysosomal pathway through size effect molecularly imprinted polymer (MIP) pharmacological action quercetin (QUE). Moreover, not only reduced triglyceride reverse hepatic steatosis but also effectively lowered level oxidative stress reduce hepatocellular damage. Targeting key causative factors NAFLD, offers strategy control process promoting lysosomal transport hepatocytes; serves as platform treatment triglyceride-related metabolic syndrome.

Язык: Английский

Sarcopenia and metabolic dysfunction associated steatotic liver disease: Time to address both DOI Open Access
Rochelle Wong, Liyun Yuan

World Journal of Hepatology, Год журнала: 2024, Номер 16(6), С. 871 - 877

Опубликована: Июнь 19, 2024

Sarcopenia and metabolic dysfunction associated steatotic liver disease (MASLD) are closely intertwined. Sarcopenia, traditionally a of the older adult chronic population, has been studied as one pathophysiologic conditions at play in development MASLD. They share similar risk factors insulin resistance physical inactivity. Given pathophysiology along liver-muscle axis, sarcopenia factor for MASLD, vice versa. Current research suggests bidirectional relationship. chronicity MASLD inflammatory disease, it can break down muscle mass lead to sarcopenia, while promotes intramuscular lipid accumulation that releases cytokines aggravate inflammation liver. However, longest time, lack consensus definition made difficult study their relationship outcomes. A recent nomenclature update diagnosing easier researchers identify cohorts study. no gold standard technique measure or identified yet. Future studies needed reach reduce diagnostic variation. With shared between two diseases, future may also potential therapeutic targets axis would benefit both order maximize

Язык: Английский

Процитировано

6

In vitro antioxidant effects and in vivo hepatoprotective effects of Osbeckia octandra, Vernonia cinerea and Atalantia ceylanica on a high fat diet induced metabolic dysfunction-associated steatotic liver disease mouse model DOI Creative Commons

Anuththara Upamali Abeykoon,

Madhavi Priyanka Paranagama, Kavindra Kumara Wijesundera

и другие.

BMC Complementary Medicine and Therapies, Год журнала: 2025, Номер 25(1)

Опубликована: Май 23, 2025

Язык: Английский

Процитировано

0

Effect of L-carnitine supplementation on muscle cramps in liver cirrhosis: results from a retrospective cohort study DOI Creative Commons
Gholam Reza Sivandzadeh,

Ali Shahsavari,

Elahe Meftah

и другие.

BMC Gastroenterology, Год журнала: 2025, Номер 25(1)

Опубликована: Март 9, 2025

Muscle cramps are among the common debilitating complications of liver cirrhosis. Since this complication lacks effective treatments, we aimed to evaluate effectiveness L-carnitine supplementation in reducing frequency, duration, and severity muscle patients with The present retrospective cohort was conducted on adult referred between November 2022 December 2023 a tertiary referral hospital Shiraz, Iran. Patients confirmed cirrhosis who had ≥ 4 times per month without other secondary etiologies for were evaluated inclusion. They included if they taken an oral supplement 1000 mg/day one available medical records assessment their before after starting supplement. From 702 screened, 195 (27.8%) cramps, 91 (13.0%) met inclusion criteria. respective median age duration (interquartile range (IQR)) 61.0 (16.0) 2.0 (3.0) years, 48 (53%) male. Median daily, weekly, monthly cramp frequency higher females (P-values < 0.05). We noted reduced severity, mean following (respective (IQR) absolute percentage change: 100 (100.0), 60 (88.33), 50 (75.0), (77.5), 40.0 (44.58); P-values 0.001). Additionally, completely resolved 29 (31.9%), 21 (23.1%), 13 (14.3%) supplementation. BMI correlated change all mentioned indices 0.05), (P-value = 0.042). Changes did not differ significantly males females. seems be promising therapeutic option Further studies control groups larger samples required confirm finding.

Язык: Английский

Процитировано

0

Lean-MAFLD: imperatives for updated evidence, mechanistic clarity, and methodological rigor DOI
Ling-Yu Yang, Xiaojun Zeng

Hepatology International, Год журнала: 2025, Номер unknown

Опубликована: Апрель 22, 2025

Язык: Английский

Процитировано

0

Unraveling the Metabolic Pathways Between Metabolic-Associated Fatty Liver Disease (MAFLD) and Sarcopenia DOI Open Access

Marina Ribas Losasso,

Maria Luiza Cesto Parussolo,

Antony Oliveira Silva

и другие.

International Journal of Molecular Sciences, Год журнала: 2025, Номер 26(10), С. 4673 - 4673

Опубликована: Май 14, 2025

Metabolic-Associated Fatty Liver Disease (MAFLD) is a public health concern that constantly expanding, with fast-growing prevalence, and it affects about quarter of the world's population. This condition significant risk factor for cardiovascular, hepatic, oncologic diseases, such as hypertension, hepatoma, atherosclerosis. Sarcopenia was long considered to be an aging-related syndrome, but today, acknowledged secondarily related chronic diseases metabolic cardiovascular conditions, liver among other comorbidities associated insulin resistance inflammation, besides inactivity poor nutrition. The physiopathology involving MAFLD sarcopenia has still not been solved. Inflammation, oxidative stress, mitochondrial dysfunction, seem some keys this relationship since hormone target mainly skeletal muscle. review aimed comprehensively discuss main physiological pathways involved in these conditions. are interconnected by complex network pathophysiological mechanisms, resistance, muscle tissue production capacity, inflammatory state, which contributors relationship. In addition, clinical analysis, patients manifest more severe hepatitis fibrosis when compared only MAFLD. These patients, both disorders, also present improvement their treated sarcopenia, reinforcing association between them. Lifestyle changes accompanied non-pharmacological interventions, dietary therapy increased physical activity, undoubtedly improve scenario.

Язык: Английский

Процитировано

0

Riesgo de enfermedad del hígado graso asociada a la disfunción metabólica en 44.939 trabajadores sanitarios españoles: variables asociadas DOI

Pedro Javier Tárraga Marcos,

Ángel Arturo López‐González, Emilio Martínez-Almoyna Rifá

и другие.

Medicina de Familia SEMERGEN, Год журнала: 2025, Номер 51(7), С. 102514 - 102514

Опубликована: Май 30, 2025

Язык: Английский

Процитировано

0

Triglyceride-Targeted Molecularly Imprinted Polymers Activate Lipophagy via Cargo Exchange for Nonalcoholic Fatty Liver Disease Treatment DOI

Yilin Wen,

Ping Weng,

Yueyue Li

и другие.

ACS Applied Polymer Materials, Год журнала: 2024, Номер 6(12), С. 7265 - 7277

Опубликована: Июнь 14, 2024

Lipid accumulation is a prominent pathologic feature of nonalcoholic fatty liver disease (NAFLD), which due to imbalances in triglycerides metabolism. However, none the available therapeutic strategies have been able achieve effective removal from lesion site. Herein, MIP@QUE, mimetic transporter with high affinity for triglycerides, was synthesized using molecular imprinting. The physicochemical features MIP@QUE are such that it binds and releases drug an affinity-driven reaction. In vivo vitro experiments showed metabolism promoted by dual activation autophagy-lysosomal pathway through size effect molecularly imprinted polymer (MIP) pharmacological action quercetin (QUE). Moreover, not only reduced triglyceride reverse hepatic steatosis but also effectively lowered level oxidative stress reduce hepatocellular damage. Targeting key causative factors NAFLD, offers strategy control process promoting lysosomal transport hepatocytes; serves as platform treatment triglyceride-related metabolic syndrome.

Язык: Английский

Процитировано

0