[This corrects the article DOI: 10.1016/j.apsb.2018.08.009.].

Objective To explore the biological effects and changes of metabolites of Guilu erxian glue(GLE)in vivo in the pre-vention and treatment of postmenopausal osteoporosis(PMO),based on non-targeted metabolomics.Methods Fifty SD female rats were divided into five groups using the random number table method:sham group,model group(OVX),and low-,medium-,and high-dose GLE(GLE-L,GLE-M and GLE-H)groups,with ten mice in each group.After 1 week of modeling,the drug was given by gavage,and samples were collected 8 weeks later.Bone microstructure was detected by MicroCT,bone metabolism-related indices were analyzed by immunohistochemistry(IHC),and a serum metabolite atlas was constructed using the LC-MS/MS technique to observe the distribution differences of metabolites and related pathways.Results The MicroCT results showed that GLE could increase the percentage of bone trabeculae and restore bone microstructure(P<0.05,GLE-M group vs.OVX group).IHC analysis showed that GLE could increase Runx2 expression in femur(P<0.05,GLE-M group vs.OVX group).There were four co-regulated metabolites in the sham group,GLE-H group,and OVX group,including 3-(3-methoxyphenyl)propionic acid,acetamide,Equol,and 1-oleoacyl-SN-glycerol-3-phosphocholine,which showed high expression in the sham group,low expression in the OVX group,and high expression in the GLE-M group.The KEGG pathway result showed that the main pathways involved between the sham group and OVX group were steroid hormone biosynthesis and cortisol synthesis and secretion.Tryptophan metabolism and phenylalanine metabolism were observed in the GLE group and OVX group.Conclusion GLE may prevent PMO by regulating metabolites in the body.

Ischemic heart disease(IHD)is one of the major threats to global health,characterized by complex and incompletely elucidated pathogenesis.Recently,with the continuous advancement of epige-netic research,lactylation(Kla),a newly discovered type of protein post-translational modification,has gradually attracted attention.Kla significantly influences the pathophysiological processes and cellular molecular functions of IHD by directly affecting gene transcription,signal transduction,and metabolic pathways.Kla extensively occurs in both histones and non-histone proteins and participates in regulating protein functions involved in various pathological processes.By modulating enzymatic activities and signal transduction pathways,Kla affects multiple processes in cardiomyocytes,including energy metabolism,inflammatory response,angiogenesis,lipid metabolic disorders,apoptosis,fibrosis,and myocardial re-pair.Although current studies on specific mechanisms and therapeutic targets of Kla in IHD remain limit-ed,its potential therapeutic value cannot be overlooked.This review summarizes the mechanisms and re-search progress of Kla in critical pathological stages of IHD,such as myocardial infarction,myocardial is-chemia-reperfusion injury,heart failure,and cardiac hypertrophy.Furthermore,we discuss the potential therapeutic targets and application prospects of Kla,aiming to provide insights and directions for identif-ying effective intervention strategies and opening new avenues for the prevention and treatment of IHD.

Objective To explore the biological effects and changes of metabolites of Guilu erxian glue(GLE)in vivo in the pre-vention and treatment of postmenopausal osteoporosis(PMO),based on non-targeted metabolomics.Methods Fifty SD female rats were divided into five groups using the random number table method:sham group,model group(OVX),and low-,medium-,and high-dose GLE(GLE-L,GLE-M and GLE-H)groups,with ten mice in each group.After 1 week of modeling,the drug was given by gavage,and samples were collected 8 weeks later.Bone microstructure was detected by MicroCT,bone metabolism-related indices were analyzed by immunohistochemistry(IHC),and a serum metabolite atlas was constructed using the LC-MS/MS technique to observe the distribution differences of metabolites and related pathways.Results The MicroCT results showed that GLE could increase the percentage of bone trabeculae and restore bone microstructure(P<0.05,GLE-M group vs.OVX group).IHC analysis showed that GLE could increase Runx2 expression in femur(P<0.05,GLE-M group vs.OVX group).There were four co-regulated metabolites in the sham group,GLE-H group,and OVX group,including 3-(3-methoxyphenyl)propionic acid,acetamide,Equol,and 1-oleoacyl-SN-glycerol-3-phosphocholine,which showed high expression in the sham group,low expression in the OVX group,and high expression in the GLE-M group.The KEGG pathway result showed that the main pathways involved between the sham group and OVX group were steroid hormone biosynthesis and cortisol synthesis and secretion.Tryptophan metabolism and phenylalanine metabolism were observed in the GLE group and OVX group.Conclusion GLE may prevent PMO by regulating metabolites in the body.

Body weight abnormalities, including overweight, obesity, and underweight, have become a dual public health challenge in Chinese adults: overweight and obesity lead to a variety of chronic complications, while underweight increases the risks of malnutrition, sarcopenia, and organ dysfunction. To systematically address these issues, multidisciplinary experts in endocrinology, sports science, nutrition, and psychiatry from various regions have held multiple weight management seminars. Based on the latest epidemiological data and clinical evidence, they expanded the guideline to include assessment and intervention strategies for underweight, in addition to the core content of obesity management. This guideline outlines the etiological mechanisms, evaluation methods, and multidimensional management strategies for overweight and obesity, covering key areas such as diagnosis and assessment, medical nutrition therapy, exercise prescription, pharmacological intervention, and psychological support. It is intended to provide a scientific and standardized approach to weight management across the adult population, aiming to curb the rising prevalence of obesity, mitigate complications associated with abnormal body weight, and improve nutritional status and overall quality of life.

Ischemic heart disease(IHD)is one of the major threats to global health,characterized by complex and incompletely elucidated pathogenesis.Recently,with the continuous advancement of epige-netic research,lactylation(Kla),a newly discovered type of protein post-translational modification,has gradually attracted attention.Kla significantly influences the pathophysiological processes and cellular molecular functions of IHD by directly affecting gene transcription,signal transduction,and metabolic pathways.Kla extensively occurs in both histones and non-histone proteins and participates in regulating protein functions involved in various pathological processes.By modulating enzymatic activities and signal transduction pathways,Kla affects multiple processes in cardiomyocytes,including energy metabolism,inflammatory response,angiogenesis,lipid metabolic disorders,apoptosis,fibrosis,and myocardial re-pair.Although current studies on specific mechanisms and therapeutic targets of Kla in IHD remain limit-ed,its potential therapeutic value cannot be overlooked.This review summarizes the mechanisms and re-search progress of Kla in critical pathological stages of IHD,such as myocardial infarction,myocardial is-chemia-reperfusion injury,heart failure,and cardiac hypertrophy.Furthermore,we discuss the potential therapeutic targets and application prospects of Kla,aiming to provide insights and directions for identif-ying effective intervention strategies and opening new avenues for the prevention and treatment of IHD.

Body weight abnormalities, including overweight, obesity, and underweight, have become a dual public health challenge in Chinese adults: overweight and obesity lead to a variety of chronic complications, while underweight increases the risks of malnutrition, sarcopenia, and organ dysfunction. To systematically address these issues, multidisciplinary experts in endocrinology, sports science, nutrition, and psychiatry from various regions have held multiple weight management seminars. Based on the latest epidemiological data and clinical evidence, they expanded the guideline to include assessment and intervention strategies for underweight, in addition to the core content of obesity management. This guideline outlines the etiological mechanisms, evaluation methods, and multidimensional management strategies for overweight and obesity, covering key areas such as diagnosis and assessment, medical nutrition therapy, exercise prescription, pharmacological intervention, and psychological support. It is intended to provide a scientific and standardized approach to weight management across the adult population, aiming to curb the rising prevalence of obesity, mitigate complications associated with abnormal body weight, and improve nutritional status and overall quality of life.

Caveolin-1 (Cav-1) is the main component of caveolin,which can participate in physiological processes such as endocytosis,lipid transport and signal transduction.In recent years,more and more studies have found that the ubiquitination modification of Cav-1 can not only affect the level of Cav-1 it-self,but also cause conformational changes of interacting molecules by changing the protein structure,and then play various roles in different diseases.Cav-1 contains 12 lysine residues,of which 6 lysine res-idues in the N-terminal domain (5/26/30/39/47/57) are essential for the ubiquitination of Cav-1.The types and sites of ubiquitination of Cav-1 are different in diseases,and ubiquitination can be degraded by the ubiquitin-proteasome system and lysosomal pathway.In this paper,we reviewed the relevant studies of Cav-1 ubiquitination in respiratory,digestive,neurological,endocrine,mammary reproduction and other systemic diseases,and found that Cav-1 ubiquitination mainly involves tumor,inflammation,meta-bolic diseases and other disease processes.By reviewing the role of Cav-1 ubiquitination in different dis-ease models and cells,it is hoped to deepen the understanding of the physiological and pathophysiological significance of Cav-1 ubiquitination,and provide directions for possible future interventions.

Caveolin-1 (Cav-1) is the main component of caveolin,which can participate in physiological processes such as endocytosis,lipid transport and signal transduction.In recent years,more and more studies have found that the ubiquitination modification of Cav-1 can not only affect the level of Cav-1 it-self,but also cause conformational changes of interacting molecules by changing the protein structure,and then play various roles in different diseases.Cav-1 contains 12 lysine residues,of which 6 lysine res-idues in the N-terminal domain (5/26/30/39/47/57) are essential for the ubiquitination of Cav-1.The types and sites of ubiquitination of Cav-1 are different in diseases,and ubiquitination can be degraded by the ubiquitin-proteasome system and lysosomal pathway.In this paper,we reviewed the relevant studies of Cav-1 ubiquitination in respiratory,digestive,neurological,endocrine,mammary reproduction and other systemic diseases,and found that Cav-1 ubiquitination mainly involves tumor,inflammation,meta-bolic diseases and other disease processes.By reviewing the role of Cav-1 ubiquitination in different dis-ease models and cells,it is hoped to deepen the understanding of the physiological and pathophysiological significance of Cav-1 ubiquitination,and provide directions for possible future interventions.

Objective: To investigate the causes and management of long-term persistent pelvic presacral space infection. Methods: Clinical data of 10 patients with persistent presacral infection admitted to the Cancer Hospital of Zhengzhou University from October 2015 to October 2020 were collected. Different surgical approaches were used to treat the presacral infection according to the patients' initial surgical procedures. Results: Among the 10 patients, there were 2 cases of presacral recurrent infection due to rectal leak after radiotherapy for cervical cancer, 3 cases of presacral recurrent infection due to rectal leak after radiotherapy for rectal cancer Dixons, and 5 cases of presacral recurrent infection of sinus tract after adjuvant radiotherapy for rectal cancer Miles. Of the 5 patients with leaky bowel, 4 had complete resection of the ruptured nonfunctional bowel and complete debridement of the presacral infection using an anterior transverse sacral incision with a large tipped omentum filling the presacral space; 1 had continuous drainage of the anal canal and complete debridement of the presacral infection using an anterior transverse sacral incision. 5 post-Miles patients all had debridement of the presacral infection using an anterior transverse sacral incision combined with an abdominal incision. The nine patients with healed presacral infection recovered from surgery in 26 to 210 days, with a median time of 55 days. Conclusions: Anterior sacral infections in patients with leaky gut are caused by residual bowel secretion of intestinal fluid into the anterior sacral space, and in post-Miles patients by residual anterior sacral foreign bodies. An anterior sacral caudal transverse arc incision combined with an abdominal incision is an effective surgical approach for complete debridement of anterior sacral recalcitrant infections.
Humans ; Reinfection ; Rectum/surgery* ; Rectal Neoplasms/surgery* ; Drainage ; Anal Canal/surgery* ; Pelvic Infection