Development of piperine nanoparticles stabilized by OSA modified starch through wet-media milling technique with enhanced anti-adipogenic effect in 3T3-L1 adipocytes.

Piperine (PIP) has been known for its pharmacological activities with low water solubility and poor dissolution, which limits its nutritional application. The purpose of this research was to enhance PIP stability, dispersibility and biological activity by preparing PIP nanoparticles using the wet-media milling approach combined with nanosuspension solidification methods of spray/freeze drying. Octenyl succinic anhydride (OSA)-modified waxy maize starch was applied as the stabilizer to suppress aggregation of PIP nanoparticles. The particle size, redispersibility, storage stability and in vitro release behavior of PIP nanoparticles were measured. The regulating effect on adipocyte differentiation was evaluated using 3T3-L1 cell model. Results showed that PIP nanoparticles had a reduced particle size of 60 ± 1 nm, increased release rate in the simulated gastric (SGF) and intestinal fluids (SIF) and enhanced inhibition effect on adipogenesis in 3T3-L1 cells compared with free PIP, indicating that PIP-loaded nanoparticles with improved stability and anti-adipogenic property were developed successfully by combining wet-media milling and drying methods.

Intelligent assessment of atrial fibrillation gradation based on sinus rhythm electrocardiogram and baseline information.

BACKGROUND: Atrial fibrillation (AF) is a progressive arrhythmia that significantly affects a patient's quality of life. The 4S-AF scheme is clinically recommended for AF management; however, the evaluation process is complex and time-consuming. This renders its promotion in primary medical institutions challenging. This retrospective study aimed to simplify the evaluation process and present an objective assessment model for AF gradation. METHODS: In total, 189 12-lead electrocardiogram (ECG) recordings from 64 patients were included in this study. The data were annotated into two groups (mild and severe) according to the 4S-AF scheme. Using a preprocessed ECG during the sinus rhythm (SR), we obtained a synthesized vectorcardiogram (VCG). Subsequently, various features were calculated from both signals, and age, sex, and medical history were included as baseline characteristics. Different machine learning models, including support vector machines, random forests (RF), and logistic regression, were finally tested with a combination of feature selection techniques. RESULTS: The proposed method demonstrated excellent performance in the classification of AF gradation. With an optimized feature set of VCG and baseline features, the RF model achieved accuracy, sensitivity, and specificity of 83.02 %, 80.56 %, and 88.24 %, respectively, under the inter-patient paradigm. CONCLUSION: Our results demonstrate the value of physiological signals in AF gradation evaluation, and VCG signals were effective in identifying mild and severe AF. Considering its low computational complexity and high assessment performance, the proposed model is expected to serve as a useful prognostic tool for clinical AF management.

Piperine Attenuates Bmal1-Mediated Glucose Metabolism Disorder in a Trpv1-Dependent Manner in HepG2 Cells.

Piperine (PIP), a pungent alkaloid found in black pepper, has various pharmacological effects by activating the transient receptor potential vanilloid 1 (TRPV1) receptor. In this study, the regulating effect of PIP on glucose metabolism and the underlying mechanism were examined using an insulin-resistant cell model. Results showed that PIP alleviated glucosamine (GlcN)-induced glucose metabolism disorder (from 59.19 ± 1.90 to 88.36 ± 6.57%), restored cellular redox balance (from 148.43 ± 3.52 to 110.47 ± 3.52%), improved mitochondrial function (from 63.76 ± 4.87 to 85.98 ± 5.12%), and mitigated circadian disruption in HepG2 cells via the mediation of circadian clock gene Bmal1. After the knockdown of the Trpv1 gene, the modulating effect of PIP on Bmal1-mediated glucose metabolism was weakened, indicating that PIP alleviated Bmal1-involved insulin resistance and circadian misalignment in a Trpv1-dependent manner in HepG2 cells.