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Ozone therapy for knee osteoarthritis: a literature visualization analysis of research hotspots and prospects. 臭氧治疗膝关节骨性关节炎:文献可视化分析研究热点及展望。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2024-12-07 DOI: 10.4103/mgr.MEDGASRES-D-24-00099
Qing Liu, Jian Liu, Guanglei Cao, Yuan Liu, Ye Huang, Xieyuan Jiang
{"title":"Ozone therapy for knee osteoarthritis: a literature visualization analysis of research hotspots and prospects.","authors":"Qing Liu, Jian Liu, Guanglei Cao, Yuan Liu, Ye Huang, Xieyuan Jiang","doi":"10.4103/mgr.MEDGASRES-D-24-00099","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00099","url":null,"abstract":"<p><p>Medical ozone is a molecule composed of three oxygen atoms with anti-inflammatory, analgesic, and antioxidant functions. Ozone therapy (O 3 or O 2 - O 3 ) for knee osteoarthritis has gradually received increasing attention from researchers in recent years. Here, we discuss the research hotspots and development trends of ozone therapy for knee osteoarthritis through literature visualization and analysis. (1) From 2012 to the present, the overall trend of publications on ozone treatment for knee osteoarthritis has been increasing annually, and it has received widespread attention, especially in Iran and China. (2) Keyword analysis revealed that the keywords with the greatest number of citations for ozone treatment of knee osteoarthritis are \"osteoarthritis,\" \"ozone,\" \"knee osteoarthritis,\" \"ozone therapy,\" and \"hyaluronic acid.\" (3) The results of the cocitation analysis revealed that the themes of the cocited literature are concentrated in 11 directions: intra-articular injections, intra-articular oxygen ozone, treatment of knee osteoarthritis, rehabilitation studies, time effects, pain function, comprehensive review, growth factors, rheumatic diseases, ultrasound-guided corticosteroid injections, and placebo. (4) The hotspots of the available highly cited literature have focused mainly on the efficacy and safety of ozone or growth factors alone in the treatment of knee osteoarthritis. Most of the literature suggests that intra-articular injections are the most common form of ozone therapy, and the accuracy and safety of ozone injections can be ensured using ultrasound-guided techniques. Ozone therapy has a positive short-term effect on pain control and functional recovery within 6 months after injection, but how to maintain the long-term efficacy of ozone therapy has rarely been described. It is hypothesized that the combination of ozone and growth factors may be beneficial for prolonging the efficacy of ozone therapy. (5) Ozone therapy has no advantages over other therapies in terms of therapeutic efficacy. Compared with ozone therapy, platelet-rich plasma and growth factor-rich plasma have better long-term outcomes in the treatment of knee osteoarthritis, whereas stromal vascular components have the best effects on pain relief and functional improvement. Few studies address the combination of ozone and growth factors for the treatment of knee osteoarthritis, and a few clinical studies registered have explored other treatments (e.g., corticosteroids). (6) Future studies could further explore the specific mechanisms and optimal dosing regimens of ozone combined with different growth factors in the treatment of knee osteoarthritis to compensate for the short-term efficacy of ozone therapy and to validate the long-term efficacy and safety of this combination therapy. It is also imperative to develop international guidelines for ozone therapy for osteoarthritis of the knee as soon as possible.</p>","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":" ","pages":"356-365"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918477/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142794923","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Risks of perturbed oxygen homeostasis: responses and adaptations to hyperoxia and hypoxia. 氧稳态紊乱的风险:对高氧和低氧的反应和适应。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2024-12-07 DOI: 10.4103/mgr.MEDGASRES-D-24-00075
Johannes Burtscher, Tobias Dünnwald, Martin Faulhaber, Wolfgang Schobersberger, Michele Samaja, Martin Burtscher, Martin Kopp
{"title":"Risks of perturbed oxygen homeostasis: responses and adaptations to hyperoxia and hypoxia.","authors":"Johannes Burtscher, Tobias Dünnwald, Martin Faulhaber, Wolfgang Schobersberger, Michele Samaja, Martin Burtscher, Martin Kopp","doi":"10.4103/mgr.MEDGASRES-D-24-00075","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00075","url":null,"abstract":"","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":"15 2","pages":"189-190"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918457/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143605607","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Latanoprostene bunod: the first nitric oxide-donating antiglaucoma medication. 拉坦前列腺素:第一种一氧化氮供体抗青光眼药物。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2024-12-07 DOI: 10.4103/mgr.MEDGASRES-D-24-00023
Ghazaleh Soltani, Wesam Shamseldin Shalaby, Reza Razeghinejad
{"title":"Latanoprostene bunod: the first nitric oxide-donating antiglaucoma medication.","authors":"Ghazaleh Soltani, Wesam Shamseldin Shalaby, Reza Razeghinejad","doi":"10.4103/mgr.MEDGASRES-D-24-00023","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00023","url":null,"abstract":"<p><p>Glaucoma is a chronic optic neuropathy that causes characteristic visual field defects and is considered one of the leading causes of irreversible vision loss worldwide. Lowering intraocular pressure is the only proven treatment for glaucoma. Medical therapy is usually the first-line treatment for open-angle glaucoma and ocular hypertension. Latanoprostene bunod ophthalmic drop 0.024% is a nitric oxide-donating prostaglandin F2α analog. It lowers the intraocular pressure via a dual mechanism of enhancing aqueous humor outflow through both the trabecular meshwork and uveoscleral pathways. Additionally, the nitric oxide component has shown promise in regulating ocular blood flow and promoting the survival of retinal ganglionic cells. Herein, the mechanism of action, efficacy, safety, and tolerability of the latanoprostene bunod and its effects on ocular blood flow are reviewed. Latanoprostene bunod has demonstrated strong efficacy and a favorable safety profile in both clinical trials and real-world studies. Given the promising results of latanoprostene bunod and advancements in drug delivery, topical fixed-combination and sustained-release formulations containing latanoprostene bunod and other agents targeting different intraocular pressure-lowering mechanisms may become available in the future.</p>","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":"15 2","pages":"220-227"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918484/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143008298","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Heme oxygenase/carbon monoxide system affects the placenta and preeclampsia. 血红素加氧酶/一氧化碳系统影响胎盘和先兆子痫。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2025-01-18 DOI: 10.4103/mgr.MEDGASRES-D-24-00081
Vicki L Mahan
{"title":"Heme oxygenase/carbon monoxide system affects the placenta and preeclampsia.","authors":"Vicki L Mahan","doi":"10.4103/mgr.MEDGASRES-D-24-00081","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00081","url":null,"abstract":"<p><p>Preeclampsia affects 2% to 8% of pregnancies worldwide and results in significantly high maternal and perinatal morbidity and mortality, with delivery being the only definitive treatment. It is not a single disorder, but rather a manifestation of an insult(s) to the uteroplacental unit -whether maternal, fetal, and/or placental. Multiple etiologies have been implicated, including uteroplacental ischemia, maternal infection and/or inflammation, maternal obesity, sleep disorders, hydatidiform mole, maternal intestinal dysbiosis, autoimmune disorders, fetal diseases, breakdown of maternal-fetal immune tolerance, placental aging, and endocrine disorders. Early- and late-onset preeclampsia are associated with different etiologies: early-onset preeclampsia develops because of poor placentation, while late-onset preeclampsia occurs in women with latent maternal endothelial dysfunction. In preeclamptic placentas, acquired, genetic, and immune risk factors may result in impaired trophoblast invasion and spiral artery remodeling, which affects uteroplacental perfusion. The resulting placental hypoxia affects the heme oxygenase system-a known stress response pathway affected by hypoxia that is important during normal pregnancy and may offer a therapeutic approach in preeclampsia. This review will address the effect of the heme oxygenase/carbon monoxide system on the placenta and preeclampsia.</p>","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":"15 2","pages":"276-287"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918472/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143008290","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Integration of IoT into medical gas monitoring management systems contributes to enhancing safety and operational efficiency. 将物联网集成到医用气体监测管理系统中,有助于提高安全性和运行效率。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2025-01-18 DOI: 10.4103/mgr.MEDGASRES-D-24-00132
Chitaranjan Mahapatra
{"title":"Integration of IoT into medical gas monitoring management systems contributes to enhancing safety and operational efficiency.","authors":"Chitaranjan Mahapatra","doi":"10.4103/mgr.MEDGASRES-D-24-00132","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00132","url":null,"abstract":"","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":"15 2","pages":"216-217"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918470/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143605404","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Sodium-glucose cotransporter-2 inhibitors in cardiovascular disease: a gaseous solution. 钠-葡萄糖共转运蛋白-2抑制剂在心血管疾病中的作用:一种气态溶液。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2025-01-18 DOI: 10.4103/mgr.MEDGASRES-D-24-00097
William Durante
{"title":"Sodium-glucose cotransporter-2 inhibitors in cardiovascular disease: a gaseous solution.","authors":"William Durante","doi":"10.4103/mgr.MEDGASRES-D-24-00097","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00097","url":null,"abstract":"","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":"15 2","pages":"206-207"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918474/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143605612","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
H 2 protects H9c2 cells from hypoxia/reoxygenation injury by inhibiting the Wnt/CX3CR1 signaling pathway. H2 通过抑制 Wnt/CX3CR1 信号通路保护 H9c2 细胞免受缺氧/复氧损伤。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2024-11-08 DOI: 10.4103/mgr.MEDGASRES-D-24-00027
Jingsheng Wang, Bin Ma, Xue Jiang, Chao Li, Zhaochen Lin, Yumei Wang, Jingfei Shi, Gang Wang, Chao Cui
{"title":"H 2 protects H9c2 cells from hypoxia/reoxygenation injury by inhibiting the Wnt/CX3CR1 signaling pathway.","authors":"Jingsheng Wang, Bin Ma, Xue Jiang, Chao Li, Zhaochen Lin, Yumei Wang, Jingfei Shi, Gang Wang, Chao Cui","doi":"10.4103/mgr.MEDGASRES-D-24-00027","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00027","url":null,"abstract":"<p><p>Myocardial ischemia‒reperfusion injury is a severe cardiovascular disease, and its treatment and prevention are crucial for improving patient prognosis and reducing the economic burden. This study aimed to explore the impact of hydrogen (H 2 ) on hypoxia/reoxygenation (H/R) injury in H9c2 cells (derived from rat embryonic heart tissue) induced by hydrogen peroxide (H 2 O 2 ) and to elucidate its underlying mechanism. An H/R injury model was established in H9c2 cells via exposure to 15 μM H 2 O 2 for 3 hours, followed by incubation in a 5% CO 2 atmosphere at 37°C for 24 hours. Then, the cells were treated with H 2 (50%) for 6, 12 or 24 hours. The results demonstrated that H9c2 cells exposed to H 2 O 2 and subjected to H/R injury presented a marked decrease in the cell survival rate, accompanied by severe morphological alterations, such as curling and wrinkling, and elevated lactate dehydrogenase levels. Notably, H 2 mitigated H/R injury induced by H 2 O 2 in a time-dependent manner, improving the morphological damage observed in H9c2 cells and decreasing lactate dehydrogenase levels. Compared with the model group, treatment with H 2 increased the activities of antioxidant enzymes, including catalase, superoxide dismutase, and glutathione peroxidase, while concurrently reducing the level of malondialdehyde, an indicator of cellular damage. Furthermore, H 2 treatment downregulated the expression of inflammatory cytokines and inflammatory-related factors, specifically interleukin-6, high-mobility group box 1, tumor necrosis factor-alpha, and Toll-like receptor 4, in H9c2 cells post-H/R injury. Furthermore, H 2 treatment resulted in a marked decrease in the expression levels of proteins associated with the Wnt/C-X3-C-motif receptor 1 signaling pathway, such as β-catenin, glycogen synthase kinase-3 beta, adenomatous polyposis coli, and Wnt and C-X3-C-motif receptor 1. This observation suggests a potential mechanism for its protective effects against H/R injury. Therefore, H 2 exerts a protective effect against H/R injury in H9c2 cells induced by H 2 O 2 , potentially by inhibiting the activated Wnt/C-X3-C-motif receptor 1 signaling pathway. This inhibition, in turn, prevents the generation of oxidative stress, inflammatory cytokines, and inflammation-associated factors.</p>","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":" ","pages":"339-347"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918467/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142603826","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Xenon gas as a potential treatment for opioid use disorder, alcohol use disorder, and related disorders. 氙气作为阿片类药物使用障碍、酒精使用障碍及相关疾病的一种潜在治疗方法。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2025-01-13 DOI: 10.4103/mgr.MEDGASRES-D-24-00063
Marc J Kaufman, Edward G Meloni
{"title":"Xenon gas as a potential treatment for opioid use disorder, alcohol use disorder, and related disorders.","authors":"Marc J Kaufman, Edward G Meloni","doi":"10.4103/mgr.MEDGASRES-D-24-00063","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00063","url":null,"abstract":"<p><p>Xenon gas is considered to be a safe anesthetic and imaging agent. Research on its other potentially beneficial effects suggests that xenon may have broad efficacy for treating health disorders. A number of reviews on xenon applications have been published, but none have focused on substance use disorders. Accordingly, we review xenon effects and targets relevant to the treatment of substance use disorders, with a focus on opioid use disorder and alcohol use disorder. We report that xenon inhaled at subsedative concentrations inhibits conditioned memory reconsolidation and opioid withdrawal symptoms. We review work by others reporting on the antidepressant, anxiolytic, and analgesic properties of xenon, which could diminish negative affective states and pain. We discuss research supporting the possibility that xenon could prevent analgesic- or stress-induced opioid tolerance and, by so doing could reduce the risk of developing opioid use disorder. The rapid kinetics, favorable safety and side effect profiles, and multitargeting capability of xenon suggest that it could be used as an ambulatory on-demand treatment to rapidly attenuate maladaptive memory, physical and affective withdrawal symptoms, and pain drivers of substance use disorders when they occur. Xenon may also have human immunodeficiency virus and oncology applications because its effects relevant to substance use disorders could be exploited to target human immunodeficiency virus reservoirs, human immunodeficiency virus protein-induced abnormalities, and cancers. Although xenon is expensive, low concentrations exert beneficial effects, and gas separation, recovery, and recycling advancements will lower xenon costs, increasing the economic feasibility of its therapeutic use. More research is needed to better understand the remarkable repertoire of effects of xenon and its potential therapeutic applications.</p>","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":" ","pages":"234-253"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918480/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142984236","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A theoretical model for ozone therapy in depression treatment: enhancing metabotropic glutamate signaling through controlled oxidative stress. 臭氧治疗抑郁症的理论模型:通过控制氧化应激增强代谢性谷氨酸信号。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2025-01-18 DOI: 10.4103/mgr.MEDGASRES-D-24-00123
Daniele Romanello, Mauro Martinelli
{"title":"A theoretical model for ozone therapy in depression treatment: enhancing metabotropic glutamate signaling through controlled oxidative stress.","authors":"Daniele Romanello, Mauro Martinelli","doi":"10.4103/mgr.MEDGASRES-D-24-00123","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00123","url":null,"abstract":"","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":"15 2","pages":"210-211"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918475/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143605384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Nanobubbles: a bridge connecting nanomedicine and gas medicine. 纳米气泡:连接纳米医学和气体医学的桥梁。
IF 3
Medical Gas Research Pub Date : 2025-06-01 Epub Date: 2025-01-18 DOI: 10.4103/mgr.MEDGASRES-D-24-00115
Qianqian Xiao, Qingwei Jia, Muhammad Inam, Quanyu Chen, Xiao Sun
{"title":"Nanobubbles: a bridge connecting nanomedicine and gas medicine.","authors":"Qianqian Xiao, Qingwei Jia, Muhammad Inam, Quanyu Chen, Xiao Sun","doi":"10.4103/mgr.MEDGASRES-D-24-00115","DOIUrl":"10.4103/mgr.MEDGASRES-D-24-00115","url":null,"abstract":"","PeriodicalId":18559,"journal":{"name":"Medical Gas Research","volume":"15 2","pages":"214-215"},"PeriodicalIF":3.0,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918481/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143605423","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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