Publications by authors named "Zhonghua Lu"

Patients with sepsis complicated by acute respiratory distress syndrome (ARDS) face a significantly increased risk of in-hospital death. This study aimed to identify sepsis-associated genes involved in ARDS pathogenesis and discover candidate biomarkers for its diagnosis. Gene expression profiling data from the Gene Expression Omnibus database were analyzed to identify key septic ARDS genes using differential expression analysis and weighted gene co-expression network analysis.

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Background And Aims: Steroids are the standard treatment for checkpoint inhibitor-induced liver injury (ChILI). However, concerns about their adverse effects and impacts on long-term outcomes highlight the need for alternative therapies. This study aims to evaluate the effectiveness of magnesium isoglycyrrhizinate (MgIG) in combination with steroids in ChILI.

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Background: Acute pancreatitis (AP) in the intensive care unit (ICU) is linked to elevated in-hospital mortality rates. Timely identification of high-risk patients remains challenging. This study aimed to develop an interpretable machine learning model for predicting in-hospital mortality in ICU patients with AP and to identify key contributing factors.

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α-Synuclein (αSyn) aggregation via liquid-liquid phase separation (LLPS) has recently emerged as a crucial mechanism underlying amyloid fibril formation implicated in Parkinson's disease. However, comprehensive investigation of the physicochemical properties of αSyn condensate remains incomplete. Here, we demonstrate that αSyn condensates exhibit a highly negative electrostatic potential, revealed by preferential enrichment of positively charged fluorophores or fluorophore-labeled αSyn.

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Asthenozoospermia and teratozoospermia are common causes of male infertility. Despite their prevalence, the underlying metabolic mechanisms remain poorly understood. In this study, we conducted targeted metabolomic profiling of sperm samples from 131 Chinese reproductive-age men (48 normozoospermic controls, 40 asthenozoospermic patients, and 43 teratozoospermic patients) to identify distinct metabolic signatures associated with these conditions.

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Soil Temperature Wireless Sensor Networks (STWSNs) are essential for optimizing agricultural practices by providing real-time soil temperature data in cotton fields. However, current heuristic algorithms face limitations in achieving high coverage with minimal sensor nodes. This paper introduces an Adaptive Chaotic Gaussian Lens Snake Optimization Algorithm (ACGLSOA) to address this issue.

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Background: Portal hypertension is a driving factor of cirrhosis complications, but the specific molecular mechanism of portal hypertension in cirrhosis remains unclear. The aim of this study was to identify hub genes for predicting persistent progression of portal hypertension in patients with liver cirrhosis.

Methods: Related microarray datasets were obtained from the Gene Expression Omnibus database.

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Previous studies have confirmed ambient fine particulate matter (PM) as a major environmental risk factor for cardiovascular diseases (CVDs), yet the specific molecular pathways remain poorly understood. Furthermore, while physical activity benefits cardiovascular health, its protective effects against PM-induced damage need further explored. We aimed to investigate the relationship between long-term PM exposure, physical activity, and cardiovascular health, and explore the potential molecular mechanisms.

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Designer receptors exclusively activated by designer drugs (DREADDs) play important roles in neuroscience research and show great promise for future clinical interventions in neurological diseases. The Gs-coupled DREADD, rM3Ds, modulates excitability in neuron subsets that are sensitive to downstream effectors of Gs protein. However, given the non-human nature of the rM3Ds backbone, risks about potential immunogenicity and tolerability exist when considering clinical translation.

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Microglia, essential in the central nervous system (CNS), were historically considered absent from the peripheral nervous system (PNS). Here, we show a PNS-resident macrophage population that shares transcriptomic and epigenetic profiles as well as an ontogenetic trajectory with CNS microglia. This population (termed PNS microglia-like cells) enwraps the neuronal soma inside the satellite glial cell envelope, preferentially associates with larger neurons during PNS development, and is required for neuronal functions by regulating soma enlargement and axon growth.

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Real-time visualization and tracking of epileptic seizures are important for studying epilepsy pathogenesis and treating epilepsy; however, the requisite sensing is extremely challenging, primarily due to the transient and intricate nature of neural activity associated with epilepsy. The onset of epilepsy is closely correlated with increases in peroxynitrite (ONOO) levels, a reactive nitrogen species that can serve as a biomarker for epilepsy. However, the fleeting biological half-life and high reactivity of ONOO has historically impeded its direct visualization within the epileptic brain.

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Objective: To investigate the current status of long-term quality of life in patients with severe acute pancreatitis (SAP) who have been cured and discharged, and to analyze the influencing factors affecting long-term quality of life in SAP cured patients after discharge.

Methods: A retrospective collection was conducted. Patients who were received standardized treatment before being cured and discharged from the hospital admitted to the first department of critical care medcine of the Second Affiliated Hospital of Anhui Medical University from January 2017 to December 2023 were enrolled.

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Background: Sepsis and acute respiratory distress syndrome (ARDS) are common inflammatory conditions in intensive care, with ARDS significantly increasing mortality in septic patients. PANoptosis, a newly discovered form of programmed cell death involving multiple cell death pathways, plays a critical role in inflammatory diseases. This study aims to elucidate the PANoptosis-related genes (PRGs) and their involvement in the progression of sepsis to ARDS.

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Optogenetics is a valuable tool for studying the mechanisms of neurological diseases and is now being developed for therapeutic applications. In rodents and macaques, improved channelrhodopsins have been applied to achieve transcranial optogenetic stimulation. While transcranial photoexcitation of neurons has been achieved, noninvasive optogenetic inhibition for treating hyperexcitability-induced neurological disorders has remained elusive.

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Background: Caroli's disease, an autosomal recessive, hereditary-related disorder, is a rare disease, in which the diagnosis is based primarily on medical imaging and pathophysiological examinations. It is characterized by intrahepatic cystic dilation or cysts. Hepatic resection of diseased lobes can cure or avoid the risk of malignancy.

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Sepsis is one of the leading causes of death among seriously ill patients worldwide, affecting more than 30 million people annually and accounting for 1-2% of hospitalizations. By analyzing gene expression omnibus (GEO) data set, our team explored the relationship between m6A methylation gene and poor prognosis of sepsis. The purpose of this present study is to examine new detection markers for patients with poor prognosis, provide theoretical basis for timely intervention and improve the survival rate of patients.

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The preoptic area of the hypothalamus is critical for regulation of brain-body interaction, including circuits that control vital signs such as body temperature and heart rate. The preoptic area contains approximately 70 molecularly distinct cell types. The gene is expressed in a subset of preoptic area cell types.

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Background: Emphysematous pancreatitis (EP) is a rare, severe form of acute necrotizing pancreatitis characterized by gas in pancreatic or peripancreatic tissue, with a high mortality rate.

Aim: To assess the diagnosis, treatment, and outcomes of EP through a series of case studies.

Methods: This case series was conducted in intensive care units at the Second Affiliated Hospital of Anhui Medical University.

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Article Synopsis
  • A circuit-based gene therapy has effectively reversed key symptoms of Parkinson's disease in animal models, including mice and primates.
  • This approach targets dopamine receptor D-expressing neurons through a combination of adeno-associated virus (AAV) delivery and chemogenetic techniques.
  • The research includes a step-by-step guide for AAV injection, creating PD models in primates, and evaluating the therapy's impact on motor symptoms.
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Background: Members of the interferon regulatory factor (IRF) family are transcriptional regulators that play vital roles in the inflammatory response of macrophages. IRF1, IRF3, and IRF9 regulate the expression of immune-responsive gene 1 (IRG1) in macrophages. However, the role of IRF2 in the inflammatory response of macrophages remains somewhat contradictory.

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Temporal lobe epilepsy (TLE) is the most common form of medically-intractable epilepsy. Subicular hyperexcitability is frequently observed with TLE, presumably caused by impaired inhibition of local excitatory neurons. Here, we evaluated the effectiveness of silencing subicular pyramidal neurons to treat a rodent model of TLE.

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Background: The relationship between ozone (O) exposure and blood pressure (BP) remains inconclusive. Given the scarcity of Chinese epidemiological data, more research on this association is of paramount importance, particularly among middle-aged and older Chinese populations.

Methods: This study involved 10,875 participants (median age: 60.

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Neonatal birth weight is a crucial indicator of intrauterine growth and development with important implications for child development and adult health. The birth weight of a newborn is closely linked to the nutrition and health of the mother during pregnancy as well as genetic factors. Therefore, assessing the metabolic status of the fetus in utero is greatly significant for understanding the mechanisms responsible for abnormal birth weight.

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Article Synopsis
  • Scientists studied a health problem called MASH, which affects people's livers, and worked on two tests to help doctors tell if someone has it.
  • They looked at data from over 3,000 people to make sure their first test, called acMASH, worked well, and then created a new test called acFibroMASH to find more severe cases.
  • The new acFibroMASH test was better at predicting who might have future liver problems compared to another test, showing it's a useful tool for doctors to keep patients healthy.
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