Pub Date : 2025-12-31DOI: 10.3831/KPI.2025.28.4.269
Minsu Lee, Gyuwon Park, Yoonsu Tae, Eunbin Kim, Jinwoong Lim
Objectives: Lumbar disc herniation (LDH) symptoms include lower back pain (LBP), radiating leg pain, and muscle weakness in muscles innervated by the affected nerve roots. The treatment of LDH is divided into conservative and surgical treatments. In this study, we aimed to summarize and analyze the clinical studies of pharmacopuncture (PP) on LDH and to assess its utilization rate in clinical practice.
Methods: In this scoping review, we searched both the domestic (Research information sharing service [RISS], SCIENCE ON, online access to shared information system [OASIS]), and international (PubMed) databases to gather case reports, retrospective studies, and randomized controlled trials with information on the types and doses of PP by injection points up to September 3rd, 2024. The information obtained was analyzed using the PP type and dose at each injection point.
Results: Sixty-three studies were identified for this study. We observed that bee venom was most used (34 studies), followed by Shinbaro (29 studies). Studies on other PP types did not exceed four each. The PP doses ranged from a minimum of 0.04 cc to a maximum of 6.00 cc. The most used dose was 1.00 cc. Injection points were intradermal at each disc level, Ah-Shi points, tender points, muscles, traditional acupoints, and facet joints.
Conclusion: We analyzed variations in injection points and maximum doses of PP according to substance type and anatomical location. These results support the development of standardized protocols for acupoint injection therapy in patients with LDH.
{"title":"Types and Doses of Pharmacopuncture for Lumbar Disc Herniation: a scoping review of clinical studies.","authors":"Minsu Lee, Gyuwon Park, Yoonsu Tae, Eunbin Kim, Jinwoong Lim","doi":"10.3831/KPI.2025.28.4.269","DOIUrl":"10.3831/KPI.2025.28.4.269","url":null,"abstract":"<p><strong>Objectives: </strong>Lumbar disc herniation (LDH) symptoms include lower back pain (LBP), radiating leg pain, and muscle weakness in muscles innervated by the affected nerve roots. The treatment of LDH is divided into conservative and surgical treatments. In this study, we aimed to summarize and analyze the clinical studies of pharmacopuncture (PP) on LDH and to assess its utilization rate in clinical practice.</p><p><strong>Methods: </strong>In this scoping review, we searched both the domestic (Research information sharing service [RISS], SCIENCE ON, online access to shared information system [OASIS]), and international (PubMed) databases to gather case reports, retrospective studies, and randomized controlled trials with information on the types and doses of PP by injection points up to September 3rd, 2024. The information obtained was analyzed using the PP type and dose at each injection point.</p><p><strong>Results: </strong>Sixty-three studies were identified for this study. We observed that bee venom was most used (34 studies), followed by Shinbaro (29 studies). Studies on other PP types did not exceed four each. The PP doses ranged from a minimum of 0.04 cc to a maximum of 6.00 cc. The most used dose was 1.00 cc. Injection points were intradermal at each disc level, Ah-Shi points, tender points, muscles, traditional acupoints, and facet joints.</p><p><strong>Conclusion: </strong>We analyzed variations in injection points and maximum doses of PP according to substance type and anatomical location. These results support the development of standardized protocols for acupoint injection therapy in patients with LDH.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"269-289"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745367/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878548","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}
Objectives: Aniline, a widely used industrial chemical, is associated with severe anaemia and oxidative damage to the spleen, posing significant health risks through environmental and occupational exposure. Therefore, this study evaluated the therapeutic potential of bee venom (Apis mellifera intermissa) from north-eastern Algeria in mitigating these effects.
Methods: Acute anemia was induced via oral administration of aniline hydrochloride (100 mg/kg body weight), while recovery was assessed following intraperitoneal injection of bee venom (0.76 mg/kg body weight) for six days.
Results: Aniline exposure resulted in marked physiological, hematological, and biochemical impairments, including reduced body weight, food intake, red blood cell counts, and levels of hemoglobin (Hb), hematocrit (Hct), ferrous iron (Fe2+), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), index of distribution of RBC (IDR), and index of distribution of platelets (IDP), along with increased malondialdehyde (MDA) levels, and decreased reduced glutathione (GSH) level and catalase activity in spleen tissues. Histopathological analysis revealed splenomegaly, hyperplasia of the white pulp, and increased extramedullary hematopoiesis. Bee venom treatment significantly reversed these effects, restoring hematological parameters, antioxidant enzyme levels, and spleen architecture.
Conclusion: Bee venom showed potential as a natural therapeutic agent against aniline-induced anaemia and oxidative spleen damage, highlighting its antioxidative and restorative properties.
{"title":"Therapeutic Potential of Bee Venom (<i>Apis mellifera intermissa</i>) in Reversing Aniline-Induced Acute Anaemia and Spleen Oxidative Damage in Mice.","authors":"Faouzi Dahdouh, Amira Bourouba, Amina Bourouba, Khaled Belhamzaoui, Hadjer Khelifi, Nour El Houda Harrat, Houria Djebar-Berrebbah","doi":"10.3831/KPI.2025.28.4.379","DOIUrl":"10.3831/KPI.2025.28.4.379","url":null,"abstract":"<p><strong>Objectives: </strong>Aniline, a widely used industrial chemical, is associated with severe anaemia and oxidative damage to the spleen, posing significant health risks through environmental and occupational exposure. Therefore, this study evaluated the therapeutic potential of bee venom (<i>Apis mellifera intermissa</i>) from north-eastern Algeria in mitigating these effects.</p><p><strong>Methods: </strong>Acute anemia was induced via oral administration of aniline hydrochloride (100 mg/kg body weight), while recovery was assessed following intraperitoneal injection of bee venom (0.76 mg/kg body weight) for six days.</p><p><strong>Results: </strong>Aniline exposure resulted in marked physiological, hematological, and biochemical impairments, including reduced body weight, food intake, red blood cell counts, and levels of hemoglobin (Hb), hematocrit (Hct), ferrous iron (Fe<sup>2+</sup>), mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), mean corpuscular hemoglobin concentration (MCHC), index of distribution of RBC (IDR), and index of distribution of platelets (IDP), along with increased malondialdehyde (MDA) levels, and decreased reduced glutathione (GSH) level and catalase activity in spleen tissues. Histopathological analysis revealed splenomegaly, hyperplasia of the white pulp, and increased extramedullary hematopoiesis. Bee venom treatment significantly reversed these effects, restoring hematological parameters, antioxidant enzyme levels, and spleen architecture.</p><p><strong>Conclusion: </strong>Bee venom showed potential as a natural therapeutic agent against aniline-induced anaemia and oxidative spleen damage, highlighting its antioxidative and restorative properties.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"379-385"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745373/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878545","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}
Pub Date : 2025-12-31DOI: 10.3831/KPI.2025.28.4.255
Ahmed A Rawwash, Emad Ahmed Fathy Hussein, Omar Mohammad Atta
Objectives: Natural substances with healing properties, especially medicinal plants and bee-derived products, have been integral to traditional medicine systems for centuries, contributing significantly to wound care. Their value lies in both their pharmacological roots and well-documented biological activities, including infection control, inflammation reduction, antioxidative protection, and tissue regeneration. This review highlights the scientific evidence supporting the efficacy of bee products and plant-based therapies in wound care, assessing their chemical composition, biological properties, and mechanisms of action.
Methods: A wide range of medicinal plants and bee products are examined for their recognized therapeutic roles, with emphasis on their ability to prevent infection, modulate inflammation, counter oxidative stress, and promote healing. The review also considers complementary plant therapies that may enhance the effects of bee-derived substances.
Results: Evidence from experimental and clinical studies demonstrates that natural products such as honey and propolis can effectively treat chronic wounds, including diabetic foot ulcers, by supporting tissue repair and preventing complications.
Conclusion: This review affirms the therapeutic potential of bee products and medicinal plants and supports their integration into modern wound management protocols, which are increasingly being validated through scientific and clinical research.
{"title":"Bee Products and Traditional Plant Therapies for Wound Care: a comprehensive review of scientific evidence and clinical applications.","authors":"Ahmed A Rawwash, Emad Ahmed Fathy Hussein, Omar Mohammad Atta","doi":"10.3831/KPI.2025.28.4.255","DOIUrl":"10.3831/KPI.2025.28.4.255","url":null,"abstract":"<p><strong>Objectives: </strong>Natural substances with healing properties, especially medicinal plants and bee-derived products, have been integral to traditional medicine systems for centuries, contributing significantly to wound care. Their value lies in both their pharmacological roots and well-documented biological activities, including infection control, inflammation reduction, antioxidative protection, and tissue regeneration. This review highlights the scientific evidence supporting the efficacy of bee products and plant-based therapies in wound care, assessing their chemical composition, biological properties, and mechanisms of action.</p><p><strong>Methods: </strong>A wide range of medicinal plants and bee products are examined for their recognized therapeutic roles, with emphasis on their ability to prevent infection, modulate inflammation, counter oxidative stress, and promote healing. The review also considers complementary plant therapies that may enhance the effects of bee-derived substances.</p><p><strong>Results: </strong>Evidence from experimental and clinical studies demonstrates that natural products such as honey and propolis can effectively treat chronic wounds, including diabetic foot ulcers, by supporting tissue repair and preventing complications.</p><p><strong>Conclusion: </strong>This review affirms the therapeutic potential of bee products and medicinal plants and supports their integration into modern wound management protocols, which are increasingly being validated through scientific and clinical research.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"255-268"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745370/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878535","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}
Pub Date : 2025-12-31DOI: 10.3831/KPI.2025.28.4.301
Soo-Yeon Park
Objectives: The aim of this study was to evaluate the efficacy of intradermal acupuncture for the treatment of moderate to severe dry eye disease (DED).
Methods: Thirty patients with moderate to severe DED were randomly assigned (11) to either the Intradermal Acupuncture Group (IAG) or the Body Acupuncture Group (BAG). Both groups received 12 treatment sessions over four weeks (three times per week). The primary outcome was the Ocular Surface Disease Index (OSDI). Secondary outcomes included the Visual Analog Scale (VAS) for subjective symptoms, quality of life (QoL), the Schirmer I test (SIT), and general assessment. All outcomes were measured at baseline (Week 0), post-treatment (Week 4), and follow-up (Week 6).
Results: No statistically significant between-group differences were found in OSDI scores at Weeks 4 and 6 compared to baseline (p = 0.262, p = 0.105). Similarly, changes in VAS, QoL, and SIT scores showed no significant differences between groups (all p > 0.05). No serious adverse events occurred in either group.
Conclusion: Intradermal acupuncture showed comparable effectiveness to body acupuncture in relieving symptoms of moderate to severe DED, suggesting its potential as an alternative therapeutic option. While between-group differences were not definitive in this pilot study, the findings provide preliminary estimates to inform a future, properly powered non-inferiority trial aimed at determining whether IA can achieve clinically comparable outcomes with potential advantages in convenience and adherence.
目的:本研究的目的是评价皮内针刺治疗中重度干眼病(DED)的疗效。方法:将30例中重度DED患者(11例)随机分为皮内针刺组(IAG)和体针组(BAG)。两组在四周内接受12次治疗(每周3次)。主要观察指标为眼表疾病指数(OSDI)。次要结果包括主观症状的视觉模拟量表(VAS)、生活质量(QoL)、Schirmer I测试(SIT)和一般评估。在基线(第0周)、治疗后(第4周)和随访(第6周)测量所有结果。结果:第4周和第6周OSDI评分与基线比较,组间差异无统计学意义(p = 0.262, p = 0.105)。同样,各组间VAS、QoL和SIT评分的变化无显著差异(均p < 0.05)。两组均未发生严重不良事件。结论:皮内针刺在缓解中重度DED症状方面的效果与体针相当,提示其作为一种替代治疗选择的潜力。虽然在这项初步研究中,组间差异并不明确,但研究结果为未来的非劣效性试验提供了初步估计,该试验旨在确定IA是否可以达到具有方便性和依从性潜在优势的临床可比结果。
{"title":"Intradermal Acupuncture for Moderate to Severe Dry Eye Disease: a pilot randomized controlled trial.","authors":"Soo-Yeon Park","doi":"10.3831/KPI.2025.28.4.301","DOIUrl":"10.3831/KPI.2025.28.4.301","url":null,"abstract":"<p><strong>Objectives: </strong>The aim of this study was to evaluate the efficacy of intradermal acupuncture for the treatment of moderate to severe dry eye disease (DED).</p><p><strong>Methods: </strong>Thirty patients with moderate to severe DED were randomly assigned (11) to either the Intradermal Acupuncture Group (IAG) or the Body Acupuncture Group (BAG). Both groups received 12 treatment sessions over four weeks (three times per week). The primary outcome was the Ocular Surface Disease Index (OSDI). Secondary outcomes included the Visual Analog Scale (VAS) for subjective symptoms, quality of life (QoL), the Schirmer I test (SIT), and general assessment. All outcomes were measured at baseline (Week 0), post-treatment (Week 4), and follow-up (Week 6).</p><p><strong>Results: </strong>No statistically significant between-group differences were found in OSDI scores at Weeks 4 and 6 compared to baseline (p = 0.262, p = 0.105). Similarly, changes in VAS, QoL, and SIT scores showed no significant differences between groups (all p > 0.05). No serious adverse events occurred in either group.</p><p><strong>Conclusion: </strong>Intradermal acupuncture showed comparable effectiveness to body acupuncture in relieving symptoms of moderate to severe DED, suggesting its potential as an alternative therapeutic option. While between-group differences were not definitive in this pilot study, the findings provide preliminary estimates to inform a future, properly powered non-inferiority trial aimed at determining whether IA can achieve clinically comparable outcomes with potential advantages in convenience and adherence.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"301-310"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745372/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878570","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}
Pub Date : 2025-12-31DOI: 10.3831/KPI.2025.28.4.351
Lisa Dal Pozzo, Secondo Scarsella, Maria Abad Arranz, Md Forhad Shamim, Julie Stephanie Howatson, Kaium Abdul, Israt Jahan Poly
Objectives: Prostate cancer is a globally prevalent malignancy with rising resistance to conventional therapies. Although awareness and early diagnosis have improved through screening campaigns, there remains a need for alternative strategies. Silybummarianum L. (SM), or milk thistle, has emerged as a promising natural compound with reported anti-cancer potential. This study aimed to explore the mechanistic basis of SM's activity against prostate cancer using a combination of network pharmacology and molecular docking.
Methods: Core targets related to both SM and prostate cancer were identified through a network pharmacology approach. Protein-protein interaction networks, Gene Ontology (GO), and KEGG enrichment analyses were performed to interpret biological relevance. Molecular docking was used to evaluate the binding affinity of SM's bioactive components with selected targets.
Results: Key proteins identified included SRC, PIK3CD, CDK1, CCNA2, PTPN11, PTK2, RXRA, CYP2C9, and PTGS2, showing significant relevance to SM and prostate cancer. GO analysis emphasized "response to organic cyclic compounds" as a significant term. KEGG and GO enrichment analyses indicated that synaptic and neuronal pathways are central in the disease's progression. Docking simulations revealed strong interactions between core targets and SM constituents, notably (+)-silymonin and silandrin.
Conclusion: This integrated approach highlighted critical molecular targets and pathways modulated by SM, providing a basis for future experimental studies. SM shows potential as a complementary agent in prostate cancer therapy.
{"title":"In Silico Assessment of <i>Silybum marianum</i> Bioactive Compounds in Prostate Cancer Using Network Pharmacology and Molecular Docking.","authors":"Lisa Dal Pozzo, Secondo Scarsella, Maria Abad Arranz, Md Forhad Shamim, Julie Stephanie Howatson, Kaium Abdul, Israt Jahan Poly","doi":"10.3831/KPI.2025.28.4.351","DOIUrl":"10.3831/KPI.2025.28.4.351","url":null,"abstract":"<p><strong>Objectives: </strong>Prostate cancer is a globally prevalent malignancy with rising resistance to conventional therapies. Although awareness and early diagnosis have improved through screening campaigns, there remains a need for alternative strategies. <i>Silybum</i> <i>marianum</i> L. (SM), or milk thistle, has emerged as a promising natural compound with reported anti-cancer potential. This study aimed to explore the mechanistic basis of SM's activity against prostate cancer using a combination of network pharmacology and molecular docking.</p><p><strong>Methods: </strong>Core targets related to both SM and prostate cancer were identified through a network pharmacology approach. Protein-protein interaction networks, Gene Ontology (GO), and KEGG enrichment analyses were performed to interpret biological relevance. Molecular docking was used to evaluate the binding affinity of SM's bioactive components with selected targets.</p><p><strong>Results: </strong>Key proteins identified included SRC, PIK3CD, CDK1, CCNA2, PTPN11, PTK2, RXRA, CYP2C9, and PTGS2, showing significant relevance to SM and prostate cancer. GO analysis emphasized \"response to organic cyclic compounds\" as a significant term. KEGG and GO enrichment analyses indicated that synaptic and neuronal pathways are central in the disease's progression. Docking simulations revealed strong interactions between core targets and SM constituents, notably (+)-silymonin and silandrin.</p><p><strong>Conclusion: </strong>This integrated approach highlighted critical molecular targets and pathways modulated by SM, providing a basis for future experimental studies. SM shows potential as a complementary agent in prostate cancer therapy.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"351-366"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745369/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878582","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}
Pub Date : 2025-12-31DOI: 10.3831/KPI.2025.28.4.386
Soo-Yeon Park, Nguyen Cong Duc
Objectives: Acupuncture has been widely studied for its safety across multiple countries. Sterile acupuncture (SA), represented by the thumbtack needle, is commonly used due to its ease of application, minimal pain, and allowance of free movement. However, it is also associated with adverse events (AEs) such as foreign body sensation and allergic contact dermatitis. Biodegradable microneedle acupuncture (BMA) is a newly developed medical device that may overcome these limitations. This trial aims to confirm the superiority of BMA over SA (represented by the thumbtack needle) in terms of safety.
Methods: A total of 224 participants diagnosed with dry eye disease, asthenopia, ocular pain, Bell's palsy and its sequelae, or ptosis will be recruited from two hospitals. Participants will be randomly assigned to receive either BMA or SA in a 11 ratio. Acupuncture will be performed at eight standardized points bilateral GB14, TE23, EX-HN5, and ST1. Treatments will be administered three times per week for four weeks by Korean medicine doctors or residents with at least three years of clinical experience. The needles will be removed by the participants after four hours. The primary outcome is the incidence of treatment-related AEs. Secondary outcomes include vital signs, blood test results, incidence of allergic reactions, visual analog scale (VAS) scores for symptoms, quality of life, Ocular Surface Disease Index (OSDI) scores, and treatment satisfaction.
Conclusion: This trial will provide evidence regarding the safety of BMA. The results may help clinicians select a safer alternative to conventional thumbtack needles, especially for patients with sensitive skin. In addition, findings may serve as reference data for regulatory evaluation of BMA safety and efficacy.
{"title":"Comparison of the Safety and Efficacy of Biodegradable Microneedle Acupuncture and Sterile Acupuncture: study protocol for a prospective, confirmatory, superiority, multicenter, parallel, single-blinded randomized controlled trial.","authors":"Soo-Yeon Park, Nguyen Cong Duc","doi":"10.3831/KPI.2025.28.4.386","DOIUrl":"10.3831/KPI.2025.28.4.386","url":null,"abstract":"<p><strong>Objectives: </strong>Acupuncture has been widely studied for its safety across multiple countries. Sterile acupuncture (SA), represented by the thumbtack needle, is commonly used due to its ease of application, minimal pain, and allowance of free movement. However, it is also associated with adverse events (AEs) such as foreign body sensation and allergic contact dermatitis. Biodegradable microneedle acupuncture (BMA) is a newly developed medical device that may overcome these limitations. This trial aims to confirm the superiority of BMA over SA (represented by the thumbtack needle) in terms of safety.</p><p><strong>Methods: </strong>A total of 224 participants diagnosed with dry eye disease, asthenopia, ocular pain, Bell's palsy and its sequelae, or ptosis will be recruited from two hospitals. Participants will be randomly assigned to receive either BMA or SA in a 11 ratio. Acupuncture will be performed at eight standardized points bilateral GB14, TE23, EX-HN5, and ST1. Treatments will be administered three times per week for four weeks by Korean medicine doctors or residents with at least three years of clinical experience. The needles will be removed by the participants after four hours. The primary outcome is the incidence of treatment-related AEs. Secondary outcomes include vital signs, blood test results, incidence of allergic reactions, visual analog scale (VAS) scores for symptoms, quality of life, Ocular Surface Disease Index (OSDI) scores, and treatment satisfaction.</p><p><strong>Conclusion: </strong>This trial will provide evidence regarding the safety of BMA. The results may help clinicians select a safer alternative to conventional thumbtack needles, especially for patients with sensitive skin. In addition, findings may serve as reference data for regulatory evaluation of BMA safety and efficacy.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"386-398"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745364/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878563","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}
Pub Date : 2025-12-31DOI: 10.3831/KPI.2025.28.4.290
Jae-Hoon Jeong, Shin-Hyung Park
Objectives: The root tuber of Lindera aggregata (LA) has been traditionally used in Korean medicine to promote qi circulation and alleviate pain. This study investigated the anti-metastatic effects of an ethanolic extract of LA (ELA) and explored its underlying molecular mechanisms.
Methods: The effect of ELA on adrenergic agonist-induced cancer cell migration and invasion was evaluated using transwell assays. The influence of ELA on Src phosphorylation induced by adrenergic agonists was assessed via Western blot analysis. Network pharmacology analysis was conducted based on the known and predicted targets of ELA, including KEGG pathway enrichment, Gene Ontology (GO) enrichment, protein-protein interaction (PPI) network construction, and disease association analysis.
Results: Migration of MDA-MB-231 breast cancer cells and Hep3B hepatocellular carcinoma cells was promoted by adrenergic agonists, including epinephrine (E), norepinephrine (NE), and isoprenaline (ISO). This effect was significantly reversed by ELA in a concentration-dependent manner. Similarly, E- and NE-induced cancer cell invasion was suppressed by ELA in a dose-dependent manner. ELA also inhibited E- and NE-stimulated Src phosphorylation, suggesting that the anti-metastatic effects of ELA are mediated through Src inactivation. Network pharmacology analysis identified Src as a central hub protein potentially mediating the effects of LA. In addition, enrichment analysis revealed significant involvement of LA targets in cancer-related pathways and cell motility processes, further supporting the experimental findings.
Conclusion: These findings suggest that ELA inhibits adrenergic agonist-induced metastatic activity in cancer cells by deactivating Src, highlighting its potential as a novel anti-metastatic therapeutic agent.
{"title":"Inhibition of Adrenergic Agonist-Induced Metastatic Potential in Cancer Cells by an Ethanolic Extract of <i>Lindera aggregata</i> Root Tuber.","authors":"Jae-Hoon Jeong, Shin-Hyung Park","doi":"10.3831/KPI.2025.28.4.290","DOIUrl":"10.3831/KPI.2025.28.4.290","url":null,"abstract":"<p><strong>Objectives: </strong>The root tuber of <i>Lindera aggregata</i> (LA) has been traditionally used in Korean medicine to promote <i>qi</i> circulation and alleviate pain. This study investigated the anti-metastatic effects of an ethanolic extract of LA (ELA) and explored its underlying molecular mechanisms.</p><p><strong>Methods: </strong>The effect of ELA on adrenergic agonist-induced cancer cell migration and invasion was evaluated using transwell assays. The influence of ELA on Src phosphorylation induced by adrenergic agonists was assessed via Western blot analysis. Network pharmacology analysis was conducted based on the known and predicted targets of ELA, including KEGG pathway enrichment, Gene Ontology (GO) enrichment, protein-protein interaction (PPI) network construction, and disease association analysis.</p><p><strong>Results: </strong>Migration of MDA-MB-231 breast cancer cells and Hep3B hepatocellular carcinoma cells was promoted by adrenergic agonists, including epinephrine (E), norepinephrine (NE), and isoprenaline (ISO). This effect was significantly reversed by ELA in a concentration-dependent manner. Similarly, E- and NE-induced cancer cell invasion was suppressed by ELA in a dose-dependent manner. ELA also inhibited E- and NE-stimulated Src phosphorylation, suggesting that the anti-metastatic effects of ELA are mediated through Src inactivation. Network pharmacology analysis identified Src as a central hub protein potentially mediating the effects of LA. In addition, enrichment analysis revealed significant involvement of LA targets in cancer-related pathways and cell motility processes, further supporting the experimental findings.</p><p><strong>Conclusion: </strong>These findings suggest that ELA inhibits adrenergic agonist-induced metastatic activity in cancer cells by deactivating Src, highlighting its potential as a novel anti-metastatic therapeutic agent.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"290-300"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745366/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878568","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}
Objectives: This study aimed to develop and optimize a topical organogel formulation of Sertaconazole nitrate (SN) using Cinnamon oil (CO) to enhance antifungal activity and improve dermal drug delivery.
Methods: A 33 Box-Behnken design (BBD) was used to optimize the formulation by varying three factors- Cinnamon oil, Carbopol-934 (CP), and Polyethylene glycol-400 (PEG) at three levels. Key responses measured were viscosity (VS), spreadability (SP), and drug content (DC). The formulations underwent physicochemical evaluations including homogeneity, pH, swelling index, moisture content, and extrudability.
Results: The organogels had a skin-friendly pH ranging from 6.11 to 6.99, VS between 0.39 and 0.49 Pa.s, and SP from 20.40 to 26.45 g.cm/s-1. DC was consistently high (91.66% to 99.33%). The optimized batch (C11) showed excellent in vitro and ex vivo drug release (97.98% and 86.14%, respectively). Zeta potential of -24.60 mV indicated good physical stability. Drug deposition studies confirmed efficient skin penetration, with 85.45% retained in skin layers. Antifungal tests demonstrated strong activity against Candida albicans and Trichophyton rubrum, outperforming plain organogels and marketed formulations. Skin irritation and histopathology studies confirmed the formulation's safety for topical use.
Conclusion: The optimized Sertaconazole nitrate organogel (SNO) with CO is a stable, safe, and effective topical delivery system that enhances drug penetration and antifungal efficacy, making it a promising option for dermal antifungal therapy.
{"title":"Optimizing a Natural Oil-Based Sertaconazole Nitrate Organogel: enhanced antifungal activity through <i>in vitro</i> and <i>in vivo</i> evaluation.","authors":"Piyush Jain, Shashikant Chandrakar, Pushpa Prasad Gupta, Ravindra Kumar Pandey, Bina Gidwani","doi":"10.3831/KPI.2025.28.4.367","DOIUrl":"10.3831/KPI.2025.28.4.367","url":null,"abstract":"<p><strong>Objectives: </strong>This study aimed to develop and optimize a topical organogel formulation of Sertaconazole nitrate (SN) using Cinnamon oil (CO) to enhance antifungal activity and improve dermal drug delivery.</p><p><strong>Methods: </strong>A 3<sup>3</sup> Box-Behnken design (BBD) was used to optimize the formulation by varying three factors- Cinnamon oil, Carbopol-934 (CP), and Polyethylene glycol-400 (PEG) at three levels. Key responses measured were viscosity (VS), spreadability (SP), and drug content (DC). The formulations underwent physicochemical evaluations including homogeneity, pH, swelling index, moisture content, and extrudability.</p><p><strong>Results: </strong>The organogels had a skin-friendly pH ranging from 6.11 to 6.99, VS between 0.39 and 0.49 Pa.s, and SP from 20.40 to 26.45 g.cm/s<sup>-1</sup>. DC was consistently high (91.66% to 99.33%). The optimized batch (C11) showed excellent <i>in vitro</i> and ex vivo drug release (97.98% and 86.14%, respectively). Zeta potential of -24.60 mV indicated good physical stability. Drug deposition studies confirmed efficient skin penetration, with 85.45% retained in skin layers. Antifungal tests demonstrated strong activity against <i>Candida albicans</i> and <i>Trichophyton rubrum</i>, outperforming plain organogels and marketed formulations. Skin irritation and histopathology studies confirmed the formulation's safety for topical use.</p><p><strong>Conclusion: </strong>The optimized Sertaconazole nitrate organogel (SNO) with CO is a stable, safe, and effective topical delivery system that enhances drug penetration and antifungal efficacy, making it a promising option for dermal antifungal therapy.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"367-378"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745368/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878575","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}
Pub Date : 2025-12-31DOI: 10.3831/KPI.2025.28.4.321
Elaheh Mesdaghinia, Elham Khosravi, Hossein Akbari, Meysam Shirzad, Mohammad Mahdi Ahmadian-Attari, Mehrdad Mahdian, Mohammad Reza Memarzadeh, Mehdi Mehran, Alireza Hatami, Leila Mohammad Taghizadeh Kashani
Objectives: Bacterial vaginosis (BV) stands as one of the most prevalent causes of vaginal discharge and infection among women of reproductive age. Various medications, including metronidazole, are commonly recommended. Factors such as diminishing effectiveness and the emergence of new, resistant strains underscore the urgent need for research into alternative treatment options, including herbal remedies. This study aims to compare the efficacy of an herbal vaginal tablet (HVT) containing extracts of oregano and lemon balm to that of a metronidazole vaginal tablet.
Methods: A non-inferiority randomized triple-blind controlled trial was conducted to compare the effects of HVT with metronidazole on BV. HVT was formulated using alcoholic extracts from the aerial parts of oregano and lemon balm leaves. The primary and secondary outcomes of the study were BV clinical manifestations and Amsel's criteria, respectively. Clinical and laboratory outcome measures for both groups were assessed at three time points the beginning of the study, and again on days 5 and 10.
Results: Among the 130 participants, 54 patients from the metronidazole group and 51 from the HVT group completed the 5-day treatment period. Subsequently, 28 patients in the metronidazole group and 31 in the HVT group completed the 10-day treatment period.Regarding the clinical signs and symptoms, as well as laboratory measurements observed at the onset and on days 5 and 10 of treatment, no significant differences were found between the two groups.
Conclusion: This trial demonstrated that HVT can alleviate the clinical manifestations of BV and normalize Amsel's criteria, equal to metronidazole. Therefore, HVT can be used as a complementary herbal medicament in the management of BV.
{"title":"Efficacy of an Herbal Vaginal Tablet Containing Oregano and Lemon Balm on Bacterial Vaginosis in Comparison to Metronidazole: a non-inferiority triple-blind active-controlled trial.","authors":"Elaheh Mesdaghinia, Elham Khosravi, Hossein Akbari, Meysam Shirzad, Mohammad Mahdi Ahmadian-Attari, Mehrdad Mahdian, Mohammad Reza Memarzadeh, Mehdi Mehran, Alireza Hatami, Leila Mohammad Taghizadeh Kashani","doi":"10.3831/KPI.2025.28.4.321","DOIUrl":"10.3831/KPI.2025.28.4.321","url":null,"abstract":"<p><strong>Objectives: </strong>Bacterial vaginosis (BV) stands as one of the most prevalent causes of vaginal discharge and infection among women of reproductive age. Various medications, including metronidazole, are commonly recommended. Factors such as diminishing effectiveness and the emergence of new, resistant strains underscore the urgent need for research into alternative treatment options, including herbal remedies. This study aims to compare the efficacy of an herbal vaginal tablet (HVT) containing extracts of oregano and lemon balm to that of a metronidazole vaginal tablet.</p><p><strong>Methods: </strong>A non-inferiority randomized triple-blind controlled trial was conducted to compare the effects of HVT with metronidazole on BV. HVT was formulated using alcoholic extracts from the aerial parts of oregano and lemon balm leaves. The primary and secondary outcomes of the study were BV clinical manifestations and Amsel's criteria, respectively. Clinical and laboratory outcome measures for both groups were assessed at three time points the beginning of the study, and again on days 5 and 10.</p><p><strong>Results: </strong>Among the 130 participants, 54 patients from the metronidazole group and 51 from the HVT group completed the 5-day treatment period. Subsequently, 28 patients in the metronidazole group and 31 in the HVT group completed the 10-day treatment period.Regarding the clinical signs and symptoms, as well as laboratory measurements observed at the onset and on days 5 and 10 of treatment, no significant differences were found between the two groups.</p><p><strong>Conclusion: </strong>This trial demonstrated that HVT can alleviate the clinical manifestations of BV and normalize Amsel's criteria, equal to metronidazole. Therefore, HVT can be used as a complementary herbal medicament in the management of BV.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"321-334"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745365/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878014","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}
Objectives: Arecoline, the main bioactive compound in Areca catechu nut, interacts with nicotinic acetylcholine receptors (α4β2 and α7), suggesting potential in reducing nicotine cravings and withdrawal symptoms. This study evaluates the therapeutic potential of methanolic Areca catechu nut extract (MAN) against nicotine dependence and withdrawal in C57BL/6J mice.
Methods: A modified runway model assessed nicotine-seeking behavior. Antidopaminergic effects and locomotor activity were measured via the haloperidol-induced catalepsy model and actophotometer. Behavioral models were used to evaluate MAN's effects on nicotine withdrawal symptoms anxiety (elevated plus maze, open field, marble burying), depression (forced swim, tail suspension), social interaction, anhedonia (sucrose preference), memory (elevated plus maze), and hyperalgesia (hot plate assay).
Results: MAN (25 and 50 mg/kg, p.o.) showed antidopaminergic activity, reduced nicotine craving, and alleviated withdrawal symptoms (anxiety, depression, anhedonia, memory impairment, hyperalgesia) by enhancing serotonergic neurotransmission.
Conclusion: MAN shows potential as a therapeutic candidate for nicotine use disorder.
{"title":"Therapeutic Potential of Methanolic Extract of <i>Areca catechu</i> Nut in Treating Nicotine Use Disorder: evidence from preclinical mouse behavioral models.","authors":"Dnyaneshwari Dhananjay Vibhute, Pallavi Dorik, Anushri Jadhav, Vijayapandi Pandy","doi":"10.3831/KPI.2025.28.4.335","DOIUrl":"10.3831/KPI.2025.28.4.335","url":null,"abstract":"<p><strong>Objectives: </strong>Arecoline, the main bioactive compound in <i>Areca catechu</i> nut, interacts with nicotinic acetylcholine receptors (α4β2 and α7), suggesting potential in reducing nicotine cravings and withdrawal symptoms. This study evaluates the therapeutic potential of methanolic <i>Areca catechu</i> nut extract (MAN) against nicotine dependence and withdrawal in C57BL/6J mice.</p><p><strong>Methods: </strong>A modified runway model assessed nicotine-seeking behavior. Antidopaminergic effects and locomotor activity were measured via the haloperidol-induced catalepsy model and actophotometer. Behavioral models were used to evaluate MAN's effects on nicotine withdrawal symptoms anxiety (elevated plus maze, open field, marble burying), depression (forced swim, tail suspension), social interaction, anhedonia (sucrose preference), memory (elevated plus maze), and hyperalgesia (hot plate assay).</p><p><strong>Results: </strong>MAN (25 and 50 mg/kg, p.o.) showed antidopaminergic activity, reduced nicotine craving, and alleviated withdrawal symptoms (anxiety, depression, anhedonia, memory impairment, hyperalgesia) by enhancing serotonergic neurotransmission.</p><p><strong>Conclusion: </strong>MAN shows potential as a therapeutic candidate for nicotine use disorder.</p>","PeriodicalId":16769,"journal":{"name":"Journal of Pharmacopuncture","volume":"28 4","pages":"335-350"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12745371/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878528","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}