Pub Date : 2025-09-29DOI: 10.1080/13813455.2025.2567347
Liu Jia, Zeng Lingpiao, Hu Jiayin, Huang Qiyun, Yang Yirong
Traditional cancer diagnosis methods include imaging examinations, biopsy, etc., but these methods are often invasive, time-consuming, and costly. This study aims to explore the application effect of infra-red thermography technology in cancer diagnosis and analyse the coping experience of primary caregivers during patient diagnosis and treatment. The data collection methods include semi-structured interviews, observations, and questionnaire surveys. The research results show that infra-red thermography technology has high sensitivity and specificity in cancer diagnosis, which can assist doctors in detecting early signs of tumours. Therefore, cancer diagnosis technology based on infra-red thermography has shown great potential in early detection and is expected to become a beneficial supplement to traditional diagnostic methods. At the same time, caregivers' coping experiences during cancer diagnosis and treatment are complex and diverse, requiring the healthcare system to provide more support and resources to help them better adapt and cope.
{"title":"Qualitative study on cancer diagnosis and primary caregiver coping experience based on infra-red thermography: Impact of protein metabolism and immune function.","authors":"Liu Jia, Zeng Lingpiao, Hu Jiayin, Huang Qiyun, Yang Yirong","doi":"10.1080/13813455.2025.2567347","DOIUrl":"https://doi.org/10.1080/13813455.2025.2567347","url":null,"abstract":"<p><p>Traditional cancer diagnosis methods include imaging examinations, biopsy, etc., but these methods are often invasive, time-consuming, and costly. This study aims to explore the application effect of infra-red thermography technology in cancer diagnosis and analyse the coping experience of primary caregivers during patient diagnosis and treatment. The data collection methods include semi-structured interviews, observations, and questionnaire surveys. The research results show that infra-red thermography technology has high sensitivity and specificity in cancer diagnosis, which can assist doctors in detecting early signs of tumours. Therefore, cancer diagnosis technology based on infra-red thermography has shown great potential in early detection and is expected to become a beneficial supplement to traditional diagnostic methods. At the same time, caregivers' coping experiences during cancer diagnosis and treatment are complex and diverse, requiring the healthcare system to provide more support and resources to help them better adapt and cope.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-12"},"PeriodicalIF":2.7,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145184606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-22DOI: 10.1080/13813455.2025.2548815
Flávio André Silva, Leslie Andrews Portes, Ednei Luiz Antonio, Luis Felipe Neves Dos Santos, Helenita Antonia Oliveira, Ighor Luiz Azevedo Teixeira, André Rodrigues Lourenço Dias, Paulo José Ferreira Tucci, Andrey Jorge Serra
Background: The cardioprotective properties of resistance training (RT) in infarcted rats have been poorly investigated. This study aimed to evaluate the effects of eight weeks of RT prior myocardial infarction (MI) in rats. Method: Groups: SSh: sedentary sham surgery; SMI: sedentary MI; TMI: trained MI. At the end of the eighth week, the animals underwent either MI or sham surgery and were analysed four weeks later. Results: The TMI presented MI sizes, scar areas, masses of the atria, right ventricle, heart, left atrial area, E wave, and E/A ratio, smaller than the SMI. The protein expression related to Ca2+ handling were not affected by the RE. The maximal load (ML) of the TMI was greater than that of the SMI group. The VO2 peak and maximum speed (Vmax) were lower in the infarcted groups. Conclusion: Prior RT confers cardioprotection against cardiac remodelling by attenuating infarct size progression, myocardial hypertrophy, and diastolic dysfunction.
{"title":"Prior resistance training exerts cardioprotection against cardiac remodelling after myocardial infarction.","authors":"Flávio André Silva, Leslie Andrews Portes, Ednei Luiz Antonio, Luis Felipe Neves Dos Santos, Helenita Antonia Oliveira, Ighor Luiz Azevedo Teixeira, André Rodrigues Lourenço Dias, Paulo José Ferreira Tucci, Andrey Jorge Serra","doi":"10.1080/13813455.2025.2548815","DOIUrl":"https://doi.org/10.1080/13813455.2025.2548815","url":null,"abstract":"<p><p><b>Background</b>: The cardioprotective properties of resistance training (RT) in infarcted rats have been poorly investigated. This study aimed to evaluate the effects of eight weeks of RT prior myocardial infarction (MI) in rats. <b>Method</b>: Groups: SSh: sedentary sham surgery; SMI: sedentary MI; TMI: trained MI. At the end of the eighth week, the animals underwent either MI or sham surgery and were analysed four weeks later. <b>Results</b>: The TMI presented MI sizes, scar areas, masses of the atria, right ventricle, heart, left atrial area, E wave, and E/A ratio, smaller than the SMI. The protein expression related to Ca<sup>2+</sup> handling were not affected by the RE. The maximal load (ML) of the TMI was greater than that of the SMI group. The VO<sub>2</sub> peak and maximum speed (Vmax) were lower in the infarcted groups. <b>Conclusion</b>: Prior RT confers cardioprotection against cardiac remodelling by attenuating infarct size progression, myocardial hypertrophy, and diastolic dysfunction.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-10"},"PeriodicalIF":2.7,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145124095","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-19DOI: 10.1080/13813455.2025.2564081
Shuigen Ye, Lihua Xu, Yin Fang, Jianpei Ye, Suzhi Hu
Lipoprotein metabolic regulation plays a vital role in human health and disease, with its abnormalities closely associated with the onset and progression of various disorders. In cases of lymphadenopathy, this study aimed to develop a linear model based on multimodal ultrasound parameters and lipoprotein metabolic regulation, predicting changes in intraluminal and perilymphatic tissue stiffness during cervical lymphadenopathy to provide clinical guidance for assessing lymph node characteristics. All patients underwent multimodal ultrasound examinations including conventional 2D ultrasound, colour Doppler ultrasound, and elastography. The linear model developed based on these factors demonstrated high predictive power, indicating that changes in lipoprotein metabolism are closely linked to the pathophysiological processes of lymph nodes. In lymphadenopathy, lipoprotein metabolic regulation affects local inflammatory responses and extracellular matrix remodelling, thereby influencing lymph node stiffness and function. Additionally, lipoprotein regulation indirectly impacts lymph node hardness by modulating angiogenesis and extracellular matrix remodelling.
{"title":"Analysis of soft tissue hardness changes in cervical lymph node enlargement based on multimodal ultrasound parameters and lipid metabolism regulation.","authors":"Shuigen Ye, Lihua Xu, Yin Fang, Jianpei Ye, Suzhi Hu","doi":"10.1080/13813455.2025.2564081","DOIUrl":"https://doi.org/10.1080/13813455.2025.2564081","url":null,"abstract":"<p><p>Lipoprotein metabolic regulation plays a vital role in human health and disease, with its abnormalities closely associated with the onset and progression of various disorders. In cases of lymphadenopathy, this study aimed to develop a linear model based on multimodal ultrasound parameters and lipoprotein metabolic regulation, predicting changes in intraluminal and perilymphatic tissue stiffness during cervical lymphadenopathy to provide clinical guidance for assessing lymph node characteristics. All patients underwent multimodal ultrasound examinations including conventional 2D ultrasound, colour Doppler ultrasound, and elastography. The linear model developed based on these factors demonstrated high predictive power, indicating that changes in lipoprotein metabolism are closely linked to the pathophysiological processes of lymph nodes. In lymphadenopathy, lipoprotein metabolic regulation affects local inflammatory responses and extracellular matrix remodelling, thereby influencing lymph node stiffness and function. Additionally, lipoprotein regulation indirectly impacts lymph node hardness by modulating angiogenesis and extracellular matrix remodelling.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-8"},"PeriodicalIF":2.7,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145085013","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-05DOI: 10.1080/13813455.2025.2556008
Yuhao Yu, Jiayan Luo, Haizhong Jiang, Haojun Song, Bujiang Wang
Background: Colorectal cancer (CRC) is a highly prevalent and fatal malignancy worldwide. Despite advancements in early screening techniques and treatments, the prognosis for patients remains suboptimal. Studies have shown that metal ions play crucial roles in the occurrence, progression, and treatment of CRC.
Method: Regulating the concentrations of specific metal ions within tumour cells can promote cancer cell death and increase the effectiveness of chemotherapy, radiotherapy, targeted therapy, and immunotherapy.
Results: This article reviews the relationships between metal ions such as iron, copper, potassium, calcium, magnesium, and zinc and CRC, summarising recent research progress from mechanistic studies to clinical applications. Magnesium ions inhibit CRC development and metastasis by regulating various signalling pathways can either promote or inhibit tumour-associated gene expression.
Conclusion: Therefore, modulating the concentrations of relevant metal ions within tumour cells could be a potential therapeutic direction for CRC, providing new theoretical foundations and strategies for clinical treatment.
{"title":"Metal ions and colorectal cancer: unlocking the secrets of tumour cell death.","authors":"Yuhao Yu, Jiayan Luo, Haizhong Jiang, Haojun Song, Bujiang Wang","doi":"10.1080/13813455.2025.2556008","DOIUrl":"https://doi.org/10.1080/13813455.2025.2556008","url":null,"abstract":"<p><strong>Background: </strong>Colorectal cancer (CRC) is a highly prevalent and fatal malignancy worldwide. Despite advancements in early screening techniques and treatments, the prognosis for patients remains suboptimal. Studies have shown that metal ions play crucial roles in the occurrence, progression, and treatment of CRC.</p><p><strong>Method: </strong>Regulating the concentrations of specific metal ions within tumour cells can promote cancer cell death and increase the effectiveness of chemotherapy, radiotherapy, targeted therapy, and immunotherapy.</p><p><strong>Results: </strong>This article reviews the relationships between metal ions such as iron, copper, potassium, calcium, magnesium, and zinc and CRC, summarising recent research progress from mechanistic studies to clinical applications. Magnesium ions inhibit CRC development and metastasis by regulating various signalling pathways can either promote or inhibit tumour-associated gene expression.</p><p><strong>Conclusion: </strong>Therefore, modulating the concentrations of relevant metal ions within tumour cells could be a potential therapeutic direction for CRC, providing new theoretical foundations and strategies for clinical treatment.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-16"},"PeriodicalIF":2.7,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144999562","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Post-stroke cognitive impairment (PSCI), a common complication following stroke, significantly impacts patients' quality of life and prognosis. Research indicates that neuroregulation and protein metabolic disorders play crucial roles in the development of PSCI.
Purpose: This study aimed to evaluate the reliability of the Regional Meningoarterial Score (rLMC) in determining collateral circulation status in acute ischaemic stroke patients.
Method: Participants were selected based on specific criteria including MRI-detected recent cerebral infarction, absence of prior large-scale subcortical infarction or haemorrhage, and no history of Alzheimer's disease or cognitive impairment.
Results: The results showed that cognitive impairment group (CI group) exhibited significantly lower serum acetylcholine levels compared to normal control group (CN group), while β-amyloid protein levels were markedly higher. CI group also demonstrated reduced expression of neuroregulatory factors.
Conclusion: These findings demonstrate that neuroregulatory factors and protein metabolites can serve as potential biomarkers for early diagnosis and intervention, effectively predicting post-stroke cognitive impairment.
{"title":"Cross-sectional study on the connection between collateral status and cognitive impairment after stroke based on neural regulation and protein metabolism.","authors":"Shufen Zhang, Jiwei Cheng, Chuansen Liu, Yunyun Zhang","doi":"10.1080/13813455.2025.2556009","DOIUrl":"https://doi.org/10.1080/13813455.2025.2556009","url":null,"abstract":"<p><strong>Background: </strong>Post-stroke cognitive impairment (PSCI), a common complication following stroke, significantly impacts patients' quality of life and prognosis. Research indicates that neuroregulation and protein metabolic disorders play crucial roles in the development of PSCI.</p><p><strong>Purpose: </strong>This study aimed to evaluate the reliability of the Regional Meningoarterial Score (rLMC) in determining collateral circulation status in acute ischaemic stroke patients.</p><p><strong>Method: </strong>Participants were selected based on specific criteria including MRI-detected recent cerebral infarction, absence of prior large-scale subcortical infarction or haemorrhage, and no history of Alzheimer's disease or cognitive impairment.</p><p><strong>Results: </strong>The results showed that cognitive impairment group (CI group) exhibited significantly lower serum acetylcholine levels compared to normal control group (CN group), while β-amyloid protein levels were markedly higher. CI group also demonstrated reduced expression of neuroregulatory factors.</p><p><strong>Conclusion: </strong>These findings demonstrate that neuroregulatory factors and protein metabolites can serve as potential biomarkers for early diagnosis and intervention, effectively predicting post-stroke cognitive impairment.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-9"},"PeriodicalIF":2.7,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144999533","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-04DOI: 10.1080/13813455.2025.2555473
Naglaa Adly Abd Elazeem, Lamis Abdelghani Salamah, Marwa Abdeltawab Mohammed, Ghada Mahmoud Abd El Aziz, Shaimaa Abd El Tawab Fathi
Bisphenol-A (BPA) is an environmental pollutant that causes hepatic injury. The antioxidant activity of vildagliptin is confirmed. The present study investigated the protective effect of Vildagliptin against BPA-induced hepatotoxicity. Twenty four rats were divided randomly into 4 groups (6 rats/group): A control group, BPA group, BPA + Vildagliptin group and Vildagliptin group. All rats, except the controls were orally administered 30 mg/kg body weight BPA and/or 10 mg/kg Vildagliptin. AST, ALT, Triglycerides and albumin were measured in the serum. MDA, GPX, XBP1, Caspase 3 and BCL2 were measured in liver tissues. BPA group showed a significant decrease of albumin and GPX and a significant increase of triglycerides, AST, ALT and MDA. BPA caused up regulation of caspase3 and XBP1 while caused down regulation of BCL2. The co-administration of Vildagliptin reversed these hazards. The results of this study established the protective effect of Vildagliptin against BPA induced liver dysfunction.
{"title":"Protective role of vildagliptin against bisphenol-A induced liver injury: targeting oxidative stress, apoptosis, and endoplasmic reticulum stress.","authors":"Naglaa Adly Abd Elazeem, Lamis Abdelghani Salamah, Marwa Abdeltawab Mohammed, Ghada Mahmoud Abd El Aziz, Shaimaa Abd El Tawab Fathi","doi":"10.1080/13813455.2025.2555473","DOIUrl":"https://doi.org/10.1080/13813455.2025.2555473","url":null,"abstract":"<p><p>Bisphenol-A (BPA) is an environmental pollutant that causes hepatic injury. The antioxidant activity of vildagliptin is confirmed. The present study investigated the protective effect of Vildagliptin against BPA-induced hepatotoxicity. Twenty four rats were divided randomly into 4 groups (6 rats/group): A control group, BPA group, BPA + Vildagliptin group and Vildagliptin group. All rats, except the controls were orally administered 30 mg/kg body weight BPA and/or 10 mg/kg Vildagliptin. AST, ALT, Triglycerides and albumin were measured in the serum. MDA, GPX, XBP1, Caspase 3 and BCL2 were measured in liver tissues. BPA group showed a significant decrease of albumin and GPX and a significant increase of triglycerides, AST, ALT and MDA. BPA caused up regulation of caspase3 and XBP1 while caused down regulation of BCL2. The co-administration of Vildagliptin reversed these hazards. The results of this study established the protective effect of Vildagliptin against BPA induced liver dysfunction.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-9"},"PeriodicalIF":2.7,"publicationDate":"2025-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144991511","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Renal fibrosis is a significant factor in the progression of chronic kidney disease. This study examined how menthol affects thioacetamide (TA)-induced biochemical, molecular, and histopathological damage that leads to renal fibrosis and dysfunction.
Methods: Male Wistar rats were treated with TA (200 mg/kg, intraperitoneally) twice a week for four consecutive weeks, along with menthol (10 mg/kg, intraperitoneally) for the same duration.
Results: Menthol effectively reduced oxidative stress and inflammation in the kidneys of rats treated with TA. It also lowered the expression of TGF-β1, SMAD3, α-SMA, and KIM-1. Furthermore, menthol prevented the decline in SIRT1 mRNA expression and protein levels while increasing the expression of Nrf2. It inhibited collagen deposition and histological damage in the kidneys and prevented the rise in serum creatinine and BUN levels.
Conclusion: Menthol provides protective effects against renal fibrosis induced by thioacetamide. Its antifibrotic effects are mediated by upregulating SIRT1/Nrf2 and downregulating TGF-β1/Smad3 pathways.
{"title":"Menthol ameliorates thioacetamide-induced renal fibrosis in rats by upregulating SIRT1/Nrf2 and downregulating TGF-β1/Smad3 signalling pathways.","authors":"Elaheh Babaei, Masoumeh Asle-Rousta, Sanaz Mahmazi","doi":"10.1080/13813455.2025.2554677","DOIUrl":"https://doi.org/10.1080/13813455.2025.2554677","url":null,"abstract":"<p><strong>Introduction: </strong>Renal fibrosis is a significant factor in the progression of chronic kidney disease. This study examined how menthol affects thioacetamide (TA)-induced biochemical, molecular, and histopathological damage that leads to renal fibrosis and dysfunction.</p><p><strong>Methods: </strong>Male Wistar rats were treated with TA (200 mg/kg, intraperitoneally) twice a week for four consecutive weeks, along with menthol (10 mg/kg, intraperitoneally) for the same duration.</p><p><strong>Results: </strong>Menthol effectively reduced oxidative stress and inflammation in the kidneys of rats treated with TA. It also lowered the expression of TGF-β1, SMAD3, α-SMA, and KIM-1. Furthermore, menthol prevented the decline in SIRT1 mRNA expression and protein levels while increasing the expression of Nrf2. It inhibited collagen deposition and histological damage in the kidneys and prevented the rise in serum creatinine and BUN levels.</p><p><strong>Conclusion: </strong>Menthol provides protective effects against renal fibrosis induced by thioacetamide. Its antifibrotic effects are mediated by upregulating SIRT1/Nrf2 and downregulating TGF-β1/Smad3 pathways.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-14"},"PeriodicalIF":2.7,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144940472","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-26DOI: 10.1080/13813455.2025.2550470
Hamed Alizadeh Pahlavani, Ali Veisi
Exercise and fasting, by activating hypothalamic neurons, lead to appetite regulation, increased energy efficiency, increased brown fat cells, and weight loss. Additionally, fasting and exercise affect brain plasticity and cognitive function by reducing oxidative brain damage and increasing brain-derived neurotrophic factor (BDNF), potentially reducing the risk of neurological diseases. In humans, these lifestyle interventions can also modulate autophagy and apoptosis in lymphocytes, especially natural killer (NK) cells, T cells, and B cells, which play an important role in fighting cancer and virus-infected cells. Fasting and exercise increase the concentration of autophagic monocytes, enhance killer T lymphocytes, strengthen the immune system, and delay cancer progression. Fasting and exercise can improve metabolic and inflammatory parameters through immune-related molecules, reducing systemic inflammation. Furthermore, they are associated with changes in the composition and function of gastrointestinal microbes, including an increase in beneficial microbes and a decrease in pathogenic bacteria, along with intestinal epithelial integrity.
{"title":"Possible physiological benefits of fasting and exercise.","authors":"Hamed Alizadeh Pahlavani, Ali Veisi","doi":"10.1080/13813455.2025.2550470","DOIUrl":"https://doi.org/10.1080/13813455.2025.2550470","url":null,"abstract":"<p><p>Exercise and fasting, by activating hypothalamic neurons, lead to appetite regulation, increased energy efficiency, increased brown fat cells, and weight loss. Additionally, fasting and exercise affect brain plasticity and cognitive function by reducing oxidative brain damage and increasing brain-derived neurotrophic factor (BDNF), potentially reducing the risk of neurological diseases. In humans, these lifestyle interventions can also modulate autophagy and apoptosis in lymphocytes, especially natural killer (NK) cells, T cells, and B cells, which play an important role in fighting cancer and virus-infected cells. Fasting and exercise increase the concentration of autophagic monocytes, enhance killer T lymphocytes, strengthen the immune system, and delay cancer progression. Fasting and exercise can improve metabolic and inflammatory parameters through immune-related molecules, reducing systemic inflammation. Furthermore, they are associated with changes in the composition and function of gastrointestinal microbes, including an increase in beneficial microbes and a decrease in pathogenic bacteria, along with intestinal epithelial integrity.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-22"},"PeriodicalIF":2.7,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144940470","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-03DOI: 10.1080/13813455.2025.2542631
{"title":"Correction.","authors":"","doi":"10.1080/13813455.2025.2542631","DOIUrl":"https://doi.org/10.1080/13813455.2025.2542631","url":null,"abstract":"","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"1-2"},"PeriodicalIF":2.7,"publicationDate":"2025-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144774561","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-01Epub Date: 2025-03-31DOI: 10.1080/13813455.2025.2483910
Mohammad-Sadegh Lotfi, Hamidreza Jamali, Fatemeh B Rassouli
Background: Osteoporosis poses a global health challenge, particularly with an ageing population. Quercetin, isorhamnetin, avicularin, isoquercetin, quercitrin, and taxifolin are natural flavonoids with similar structure that induce ontogenesis.
Methods: In the present study, proteins in oestrogen signalling and bone morphogenesis were analysed, and hub genes were identified with Cytoscape, followed by pathway analysis. Then, molecular targets of flavonoids and osteoporosis-related targets were identified, and overlaps were detected. Molecular docking and dynamics simulations assessed flavonoid interactions with ERs.
Results: The study identified 14 gene products linked to osteoporosis, including ESR1 and ESR2. Enrichment analyses confirmed ESR involvement in various biological processes. SwissTargetPrediction highlighted quercetin and isorhamnetin as favourable targets for ESR1 and ESR2. Molecular docking and dynamics revealed favourable and stable binding of flavonoids to ERα and ERβ.
Conclusio: These interactions suggest therapeutic potential of natural flavonoids for osteoporosis treatment by targeting ERs, laying a foundation for future research in preclinical and clinical settings.
{"title":"Network pharmacology and <i>in silico</i> study of quercetin and structurally similar flavonoids as osteogenesis inducers that interact with oestrogen receptors.","authors":"Mohammad-Sadegh Lotfi, Hamidreza Jamali, Fatemeh B Rassouli","doi":"10.1080/13813455.2025.2483910","DOIUrl":"10.1080/13813455.2025.2483910","url":null,"abstract":"<p><strong>Background: </strong>Osteoporosis poses a global health challenge, particularly with an ageing population. Quercetin, isorhamnetin, avicularin, isoquercetin, quercitrin, and taxifolin are natural flavonoids with similar structure that induce ontogenesis.</p><p><strong>Methods: </strong>In the present study, proteins in oestrogen signalling and bone morphogenesis were analysed, and hub genes were identified with Cytoscape, followed by pathway analysis. Then, molecular targets of flavonoids and osteoporosis-related targets were identified, and overlaps were detected. Molecular docking and dynamics simulations assessed flavonoid interactions with ERs.</p><p><strong>Results: </strong>The study identified 14 gene products linked to osteoporosis, including ESR1 and ESR2. Enrichment analyses confirmed ESR involvement in various biological processes. SwissTargetPrediction highlighted quercetin and isorhamnetin as favourable targets for ESR1 and ESR2. Molecular docking and dynamics revealed favourable and stable binding of flavonoids to ERα and ERβ.</p><p><strong>Conclusio: </strong>These interactions suggest therapeutic potential of natural flavonoids for osteoporosis treatment by targeting ERs, laying a foundation for future research in preclinical and clinical settings.</p>","PeriodicalId":8331,"journal":{"name":"Archives of Physiology and Biochemistry","volume":" ","pages":"658-669"},"PeriodicalIF":2.7,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143750877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}