Ayodeji Johnson Ajibare, Olabode Oluwadare Akintoye, Oluwatobiloba Adesewa Oriowo, Abosede Mary Ayoola, Isaac Adeola Oriyomi, Joshua Favour Adedara, Favour Oluwaferanmi Oluwamoroti, Kehinde Olaniyi, Kayode Tajudeen Salami
{"title":"苦柠檬提取物通过抑制Mmp-13和通过Nrf2/Ho-1上调恢复氧化还原平衡来减轻肥胖加重的骨关节炎","authors":"Ayodeji Johnson Ajibare, Olabode Oluwadare Akintoye, Oluwatobiloba Adesewa Oriowo, Abosede Mary Ayoola, Isaac Adeola Oriyomi, Joshua Favour Adedara, Favour Oluwaferanmi Oluwamoroti, Kehinde Olaniyi, Kayode Tajudeen Salami","doi":"10.1186/s43094-025-00845-z","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Osteoarthritis, the most common joint disease, affects over 500 million people globally, especially the elderly. Due to the increasing aging population and obesity rate, obesity is expected to increase over time, making it a significant public health challenge. This study investigated the protective effects of bitter lemon extract against obesity-exacerbated osteoarthritis.</p><h3>Methods</h3><p>Thirty male Wistar rats were randomly grouped into six (<i>n</i> = 5). Group 1(control) received 1 ml/100 g water daily. Groups 2–6 were induced in obesity using a high-fat diet. Groups 3–6 were induced with osteoarthritis using 4 mg/kg sodium monoacetate. Group 4 received 40 mg/kg ibuprofen, while groups 5 and 6 received 100 mg/kg and 200 mg/kg <i>Mormordica charantia</i> (MC), respectively, orally for 18 days.</p><h3>Results</h3><p>MC Treatment conferred a marked reversal of the cardinal signs of obesity-linked osteoarthritis, restricted inflammatory markers, such as TNF-α and IL-1β, and adipokines, such as leptin. There is also a possible mechanism for MC cartilage protection by suppressing the collagen-damaging enzyme MMP-13, while reversing the cartilage-building block aggrecan suppression.</p><h3>Conclusion</h3><p>Current research suggests that bitter melon extract can serve as an alternative therapy for obesity-related Osteoarthritis. Its multi-target actions on inflammation, oxidative stress, and cartilage degradation may offer advantages over the current treatments that focus on symptom relief.</p></div>","PeriodicalId":577,"journal":{"name":"Future Journal of Pharmaceutical Sciences","volume":"11 1","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-07-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://fjps.springeropen.com/counter/pdf/10.1186/s43094-025-00845-z","citationCount":"0","resultStr":"{\"title\":\"Bitter lemon extract mitigates obesity-exacerbated osteoarthritis by suppressing Mmp-13 and restoring redox balance through Nrf2/Ho-1 upregulation\",\"authors\":\"Ayodeji Johnson Ajibare, Olabode Oluwadare Akintoye, Oluwatobiloba Adesewa Oriowo, Abosede Mary Ayoola, Isaac Adeola Oriyomi, Joshua Favour Adedara, Favour Oluwaferanmi Oluwamoroti, Kehinde Olaniyi, Kayode Tajudeen Salami\",\"doi\":\"10.1186/s43094-025-00845-z\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Osteoarthritis, the most common joint disease, affects over 500 million people globally, especially the elderly. Due to the increasing aging population and obesity rate, obesity is expected to increase over time, making it a significant public health challenge. This study investigated the protective effects of bitter lemon extract against obesity-exacerbated osteoarthritis.</p><h3>Methods</h3><p>Thirty male Wistar rats were randomly grouped into six (<i>n</i> = 5). Group 1(control) received 1 ml/100 g water daily. Groups 2–6 were induced in obesity using a high-fat diet. Groups 3–6 were induced with osteoarthritis using 4 mg/kg sodium monoacetate. Group 4 received 40 mg/kg ibuprofen, while groups 5 and 6 received 100 mg/kg and 200 mg/kg <i>Mormordica charantia</i> (MC), respectively, orally for 18 days.</p><h3>Results</h3><p>MC Treatment conferred a marked reversal of the cardinal signs of obesity-linked osteoarthritis, restricted inflammatory markers, such as TNF-α and IL-1β, and adipokines, such as leptin. There is also a possible mechanism for MC cartilage protection by suppressing the collagen-damaging enzyme MMP-13, while reversing the cartilage-building block aggrecan suppression.</p><h3>Conclusion</h3><p>Current research suggests that bitter melon extract can serve as an alternative therapy for obesity-related Osteoarthritis. Its multi-target actions on inflammation, oxidative stress, and cartilage degradation may offer advantages over the current treatments that focus on symptom relief.</p></div>\",\"PeriodicalId\":577,\"journal\":{\"name\":\"Future Journal of Pharmaceutical Sciences\",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-07-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://fjps.springeropen.com/counter/pdf/10.1186/s43094-025-00845-z\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Future Journal of Pharmaceutical Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.1186/s43094-025-00845-z\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Future Journal of Pharmaceutical Sciences","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1186/s43094-025-00845-z","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
Bitter lemon extract mitigates obesity-exacerbated osteoarthritis by suppressing Mmp-13 and restoring redox balance through Nrf2/Ho-1 upregulation
Background
Osteoarthritis, the most common joint disease, affects over 500 million people globally, especially the elderly. Due to the increasing aging population and obesity rate, obesity is expected to increase over time, making it a significant public health challenge. This study investigated the protective effects of bitter lemon extract against obesity-exacerbated osteoarthritis.
Methods
Thirty male Wistar rats were randomly grouped into six (n = 5). Group 1(control) received 1 ml/100 g water daily. Groups 2–6 were induced in obesity using a high-fat diet. Groups 3–6 were induced with osteoarthritis using 4 mg/kg sodium monoacetate. Group 4 received 40 mg/kg ibuprofen, while groups 5 and 6 received 100 mg/kg and 200 mg/kg Mormordica charantia (MC), respectively, orally for 18 days.
Results
MC Treatment conferred a marked reversal of the cardinal signs of obesity-linked osteoarthritis, restricted inflammatory markers, such as TNF-α and IL-1β, and adipokines, such as leptin. There is also a possible mechanism for MC cartilage protection by suppressing the collagen-damaging enzyme MMP-13, while reversing the cartilage-building block aggrecan suppression.
Conclusion
Current research suggests that bitter melon extract can serve as an alternative therapy for obesity-related Osteoarthritis. Its multi-target actions on inflammation, oxidative stress, and cartilage degradation may offer advantages over the current treatments that focus on symptom relief.
期刊介绍:
Future Journal of Pharmaceutical Sciences (FJPS) is the official journal of the Future University in Egypt. It is a peer-reviewed, open access journal which publishes original research articles, review articles and case studies on all aspects of pharmaceutical sciences and technologies, pharmacy practice and related clinical aspects, and pharmacy education. The journal publishes articles covering developments in drug absorption and metabolism, pharmacokinetics and dynamics, drug delivery systems, drug targeting and nano-technology. It also covers development of new systems, methods and techniques in pharmacy education and practice. The scope of the journal also extends to cover advancements in toxicology, cell and molecular biology, biomedical research, clinical and pharmaceutical microbiology, pharmaceutical biotechnology, medicinal chemistry, phytochemistry and nutraceuticals.