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IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 DOI: 10.1016/j.jaim.2024.101106
Ravindra Ghooi
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引用次数: 0
Advancing inclusive and democratic medical pluralism in Nepal 在尼泊尔推进包容和民主的医学多元化
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 DOI: 10.1016/j.jaim.2024.100988
Bamdev Subedi
Medical pluralism is a global norm rather than an exception. However, the kind of medical pluralism that exists in many settings is exclusionary and undemocratic. In many nations, medical pluralism has official acceptance, allowing both biomedicine and traditional systems of medicine a legitimate space into the formal healthcare system. However, traditional systems of medicine fall far behind biomedicine in terms of structural superiority and institutional strengths. Moreover, various forms of traditional medicine, particularly of popular variants, remain excluded from formal healthcare system, and a variety of traditional healers lack official legitimacy. Though conceptually medical pluralism sounds more or less equal standing of co-existing systems of medicine, the reality is that biomedicine enjoys a dominant status over heterodox medical systems. Upon examining the amount of budgetary allocation, number of health facilities, size of health human resources, educational institutions and research output, this paper reveals an overemphasis on biomedicine, overshadowing both scholarly and popular traditional medicine. This arrangement underscores the undemocratic and exclusionary nature of medical pluralism in the country. In light of the published data sources this paper examines the structure of medical pluralism and proposes measures that can contribute to advancing inclusive and democratic medical pluralism in Nepal.
医学多元化是全球常态而非例外。然而,存在于许多环境中的医学多元化是排斥性的、不民主的。在许多国家,医学多元化得到官方认可,生物医学和传统医学体系都可以合法地进入正规医疗系统。然而,传统医学体系在结构优势和制度优势方面远远落后于生物医学。此外,各种形式的传统医学,尤其是流行的变体,仍然被排除在正规医疗体系之外,各种传统医者也缺乏官方合法性。虽然从概念上讲,医学多元化意味着并存的医学体系或多或少处于平等地位,但实际情况是,生物医学对非正统医学体系享有主导地位。通过对预算拨款数额、卫生设施数量、卫生人力资源规模、教育机构和研究成果的研究,本文揭示了对生物医学的过度重视,使学术医学和大众传统医学都黯然失色。这种安排凸显了该国医学多元化的不民主性和排斥性。根据已公布的数据来源,本文对医学多元化的结构进行了研究,并提出了有助于推进尼泊尔包容性和民主性医学多元化的措施。
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引用次数: 0
The World Ayurveda Congress - A movement for advancement of Ayurveda. 世界阿育吠陀大会-阿育吠陀的进步运动。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 Epub Date: 2024-12-20 DOI: 10.1016/j.jaim.2024.101123
Girish Tillu, Supriya Bhalerao, Pawankumar Godatwar
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引用次数: 0
Proposed clinical algorithm for hematinic bhasmas selection for Ayurvedic pediatric care 为阿育吠陀儿科护理选择血药的拟议临床算法
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 DOI: 10.1016/j.jaim.2024.100972
K.P. Karthik , Arun Kumar Mahapatra , Prashant Kumar Gupta , S. Rajagopala
Ayurveda has unique and relevant methods in nosology, symptomatology, and drug selection. These methods need a novel and effective way of presentation for convenient comprehension and implementation. ‘Clinical algorithms’ is one such way, wherein a large amount of data is simplified, conceptual intricacies abstracted, and clinical application made easier. This article uses a modified version of the Horabin and Lewis algorithm to construct a clinical algorithm for Bhasma selection in the management of Pandu (anemia). The textual descriptions regarding the pathology and clinical presentations of Pandu have been compiled, and broadly classified, and the Bhasmas indication in suit each set of disease presentation has been specified. The algorithm is validated and optimized at single centre, while multicentre implementations and post-hoc modifications are warranted.
阿育吠陀在病名学、症状学和药物选择方面拥有独特而相关的方法。这些方法需要一种新颖有效的呈现方式,以便于理解和实施。临床算法 "就是这样一种方法,它简化了大量数据,抽象了复杂的概念,使临床应用更加容易。本文使用 Horabin 和 Lewis 算法的改进版,构建了治疗潘杜(贫血)的巴司马选择临床算法。本文对有关潘杜病理和临床表现的文字描述进行了汇编和大致分类,并明确指出了适合每种疾病表现的巴斯玛适应症。该算法在单个中心进行了验证和优化,而多中心实施和事后修改是有必要的。
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引用次数: 0
Prophylactic Ayurveda treatment for episodic cluster headache – A Case Report 发作性丛集性头痛的预防性阿育吠陀疗法--病例报告
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 DOI: 10.1016/j.jaim.2024.100994
Akshatha K. Bhat , Venugopalan Krishna kumar
This case is about an Episodic Cluster Headache (ECH) for 13 years treated effectively by Jaloukavacharana, Nasya and Ayurveda oral medications. It commenced with sudden episodic headache once or twice a day for a period of 40 days in a row, every year in the month of January and February. The pain intensity was 10/10 in numeric pain intensity scale, HIT -6 (Headache Impact Test) Score- 69, CHIQ (Cluster headache impact questionnaire) Score- 34 DASS 21 Scale- Depression- 8 anxiety-5 stress-11. Ayurveda treatment included one sitting of Jaloukavacharana and seven days of Kumkumadighrita Nasya. Drakshadi Kashaya, Soothashekararasa and Avipatthikara choorna were given internally. Patient reported no attacks of ECH thereafter with the HIT 6 score −36, CHIQ Score-0 and DASS-21 (Depression – 0, Anxiety-0, Stress- 0) after treatment. This line of treatment prevented the recurrence of ECH attacks with overall improvement in the quality of life without any known side effects.
本病例讲述的是一名发作性丛集性头痛(ECH)患者,通过 Jaloukavacharana、Nasya 和阿育吠陀口服药物得到了有效治疗,至今已有 13 年。开始时,患者会在每年的 1 月和 2 月突然发作头痛,每天一到两次,连续 40 天。疼痛强度为数字疼痛强度量表中的 10/10,HIT -6(头痛影响测试)得分- 69,CHIQ(丛集性头痛影响问卷)得分- 34,DASS 21 量表- 抑郁- 8 焦虑- 5 压力- 11。阿育吠陀疗法包括一坐 Jaloukavacharana 和七天 Kumkumadighrita Nasya。内服了 Drakshadi Kashaya、Soothashekararasa 和 Avipatthikara choorna。治疗后,患者的 HIT 6 评分-36,CHIQ 评分-0,DASS-21(抑郁-0,焦虑-0,压力-0),此后 ECH 再未发作。这种治疗方法防止了 ECH 复发,并全面改善了患者的生活质量,而且没有任何已知的副作用。
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引用次数: 0
A machine learning-based clinical decision support system for effective stratification of gestational diabetes mellitus and management through Ayurveda. 基于机器学习的临床决策支持系统,用于妊娠期糖尿病的有效分层和阿育吠陀治疗。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 Epub Date: 2024-12-10 DOI: 10.1016/j.jaim.2024.101051
Nisha P Shetty, Jayashree Shetty, Veeraj Hegde, Sneha Dattatray Dharne, Mamtha Kv

Background: Gestational Diabetes Mellitus (GDM) is a metabolic condition that develops in course of pregnancy. The World Health Organization describes it as carbohydrate intolerance that causes hyperglycemia of varying severity and manifests itself or is first noticed during pregnancy. Early prediction is now possible, owing to the application of cutting-edge methods like machine learning.

Objective: In the proposed empirical study, different machine-learning algorithms are applied to predict the prospective risk factors influencing the progression of GDM in gestating mothers.

Materials and methods: The performance of these algorithms is evaluated through accuracy, precision, f1-score, etc. The lifestyle interventions and medications listed in Ayurveda literature are discussed for effective management of the disease.

Results: Most of the proposed classifiers achieved a reasonable accuracy range of 75-82 %. Appropriate lifestyle changes, herbal remedies, decoctions, and churnas have all been shown to be useful in lowering the risk of GDM. Early detection using machine learning models can significantly reduce disease severity by facilitating timely Ayurvedic interventions.

Conclusion: The proposed work is more focused on the identification of factors impacting GDM in expectant women. A balanced diet with physical exercise, proper medication, and better lifestyle management (through Garbini Paricharya) can control the perils of GDM if diagnosed prematurely.

背景:妊娠期糖尿病(GDM)是一种在妊娠过程中发生的代谢疾病。世界卫生组织将其描述为碳水化合物不耐受,导致不同程度的高血糖,并在怀孕期间表现出来或首次发现。由于机器学习等尖端方法的应用,早期预测现在是可能的。目的:在本实证研究中,应用不同的机器学习算法预测影响妊娠期妊娠糖尿病进展的潜在危险因素。材料与方法:通过准确度、精密度、f1-score等指标来评价这些算法的性能。阿育吠陀文献中列出的生活方式干预和药物被讨论为有效的疾病管理。结果:大多数分类器达到了75- 82%的合理准确率范围。适当的生活方式改变,草药,煎剂和churnas都被证明对降低GDM的风险有用。使用机器学习模型进行早期检测可以通过促进及时的阿育吠陀干预来显着降低疾病的严重程度。结论:本研究更侧重于确定孕妇GDM的影响因素。如果过早诊断,均衡的饮食、适当的药物和更好的生活方式管理(通过Garbini Paricharya)可以控制糖尿病的危险。
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引用次数: 0
In silico exploration of phytocompounds from AYUSH-64 medicinal plants against SARS CoV-2 RNA-dependent RNA polymerase 针对 SARS CoV-2 RNA 依赖性 RNA 聚合酶的 AYUSH-64 药用植物植物化合物的硅学探索。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 DOI: 10.1016/j.jaim.2024.101026
Srinivasulu Cheemanapalli , Ramanjaneyulu Golla , Sudhakar Pagidi , Seshapani Pantangi

Background

The AYUSH 64 formulation helps to treat mild to moderate cases of COVID-19. Although several drugs have been proposed to combat COVID-19, no medication is available for SARS-CoV-2 infection. The RNA-dependent RNA polymerase (RdRp) is the pivotal enzyme of SARS-CoV-2 replication, so it could be considered a better drug target for experimental studies.

Objective

The AYUSH-64 formulation plants exhibited multiple therapeutic properties; thus, the present study aims to screen the phytocompounds of these plants against SARS CoV2 RdRp to identify specific compounds that could potentially affect COVID-19 infection.

Materials and methods

PatchDock and AutoDock tools were used for docking experiments. MD simulations and Density Functional Theory (DFT) calculations of protein-ligand Picroside-I and Remdesivir complexes were carried out in GROMACS v2019.4 and Gaussian 09 software, respectively.

Results

Among the tested, five phytocompounds (Picroside I, Oleanolic acid, Arvenin I, II, and III) from AYUSH-64 medicinal plants showed possible binding with RdRp catalytic residues (Ser759, Asp760, and Asp761). Of these, Picroside I exhibited hydrogen bond interactions with NTP entry channel residues (Arg553 and Arg555). The MM-PBSA free energy, RMSD, Rg, PCA, and RMSF analysis suggested that the Picroside I complex showed stable binding interactions with RdRp in the 50 ns simulation. In addition to this, Picroside I revealed its robust and attractive nature toward the target protein, as confirmed by DFT.

Conclusion

The results of this study have proposed that Picroside I from AYUSH 64 medicinal plant compounds was the selective binder of catalytic and NTP entry channel residues of SARS-CoV2 RdRp thereby; it may considered as a potential inhibitor of SARS-CoV2 RdRp.
背景:AYUSH 64 配方有助于治疗轻度至中度的 COVID-19 病例。虽然已经提出了几种抗 COVID-19 的药物,但还没有治疗 SARS-CoV-2 感染的药物。RNA 依赖性 RNA 聚合酶(RdRp)是 SARS-CoV-2 复制的关键酶,因此可将其视为实验研究中更好的药物靶点:AYUSH-64 配方植物具有多种治疗特性;因此,本研究旨在筛选这些植物中针对 SARS CoV2 RdRp 的植物化合物,以确定可能影响 COVID-19 感染的特定化合物:使用 PatchDock 和 AutoDock 工具进行对接实验。分别在 GROMACS v2019.4 和 Gaussian 09 软件中对蛋白质配体 Picroside-I 和 Remdesivir 复合物进行了 MD 模拟和密度泛函理论(DFT)计算:在测试的植物化合物中,来自AYUSH-64药用植物的五种植物化合物(Picroside I、齐墩果酸、Arvenin I、II和III)显示可能与RdRp催化残基(Ser759、Asp760和Asp761)结合。其中,Picroside I 与 NTP 进入通道残基(Arg553 和 Arg555)有氢键相互作用。MM-PBSA 自由能、RMSD、Rg、PCA 和 RMSF 分析表明,在 50 ns 模拟中,Picroside I 复合物与 RdRp 发生了稳定的结合相互作用。此外,经 DFT 证实,Picroside I 对目标蛋白质具有稳健的吸引力:本研究结果表明,AYUSH 64 种药用植物化合物中的 Picroside I 能选择性地结合 SARS-CoV2 RdRp 的催化和 NTP 进入通道残基,因此可被视为 SARS-CoV2 RdRp 的潜在抑制剂。
{"title":"In silico exploration of phytocompounds from AYUSH-64 medicinal plants against SARS CoV-2 RNA-dependent RNA polymerase","authors":"Srinivasulu Cheemanapalli ,&nbsp;Ramanjaneyulu Golla ,&nbsp;Sudhakar Pagidi ,&nbsp;Seshapani Pantangi","doi":"10.1016/j.jaim.2024.101026","DOIUrl":"10.1016/j.jaim.2024.101026","url":null,"abstract":"<div><h3>Background</h3><div>The AYUSH 64 formulation helps to treat mild to moderate cases of COVID-19. Although several drugs have been proposed to combat COVID-19, no medication is available for SARS-CoV-2 infection. The RNA-dependent RNA polymerase (RdRp) is the pivotal enzyme of SARS-CoV-2 replication, so it could be considered a better drug target for experimental studies.</div></div><div><h3>Objective</h3><div>The AYUSH-64 formulation plants exhibited multiple therapeutic properties; thus, the present study aims to screen the phytocompounds of these plants against SARS CoV2 RdRp to identify specific compounds that could potentially affect COVID-19 infection.</div></div><div><h3>Materials and methods</h3><div>PatchDock and AutoDock tools were used for docking experiments. MD simulations and Density Functional Theory (DFT) calculations of protein-ligand Picroside-I and Remdesivir complexes were carried out in GROMACS v2019.4 and Gaussian 09 software, respectively.</div></div><div><h3>Results</h3><div>Among the tested<strong>,</strong> five phytocompounds (Picroside I, Oleanolic acid, Arvenin I, II, and III) from AYUSH-64 medicinal plants showed possible binding with RdRp catalytic residues (Ser759, Asp760, and Asp761). Of these, Picroside I exhibited hydrogen bond interactions with NTP entry channel residues (Arg553 and Arg555). The MM-PBSA free energy, RMSD, Rg, PCA, and RMSF analysis suggested that the Picroside I complex showed stable binding interactions with RdRp in the 50 ns simulation. In addition to this, Picroside I revealed its robust and attractive nature toward the target protein, as confirmed by DFT.</div></div><div><h3>Conclusion</h3><div>The results of this study have proposed that Picroside I from AYUSH 64 medicinal plant compounds was the selective binder of catalytic and NTP entry channel residues of SARS-CoV2 RdRp thereby; it may considered as a potential inhibitor of SARS-CoV2 RdRp.</div></div>","PeriodicalId":15150,"journal":{"name":"Journal of Ayurveda and Integrative Medicine","volume":"15 6","pages":"Article 101026"},"PeriodicalIF":1.7,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142564511","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
Ayurveda treatment of nevus lipomatosus cutaneous superficialis through Ksharasutra: A case report. 阿育吠陀经穴治疗浅皮脂肪瘤1例。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 Epub Date: 2024-12-09 DOI: 10.1016/j.jaim.2024.101031
Ranjan Kumar Kasta, Ajit Kumar Pradhan, Priyanka Giri, Prasanta Kumar Sahoo
{"title":"Ayurveda treatment of nevus lipomatosus cutaneous superficialis through Ksharasutra: A case report.","authors":"Ranjan Kumar Kasta, Ajit Kumar Pradhan, Priyanka Giri, Prasanta Kumar Sahoo","doi":"10.1016/j.jaim.2024.101031","DOIUrl":"10.1016/j.jaim.2024.101031","url":null,"abstract":"","PeriodicalId":15150,"journal":{"name":"Journal of Ayurveda and Integrative Medicine","volume":"15 6","pages":"101031"},"PeriodicalIF":1.7,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11696782/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142807135","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 Ayurvedic and Allopathic treatment in hereditary breast and ovarian cancer patient with Germline BRCA1 mutation for long term disease free survival: A case report. 整合阿育吠陀和对抗疗法治疗遗传性乳腺癌和卵巢癌患者生殖系BRCA1突变的长期无病生存:1例报告。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 Epub Date: 2024-12-10 DOI: 10.1016/j.jaim.2024.100999
Sadanand Sardeshmukh, Vineeta Deshmukh, Arvind Kulkarni, Shweta Gujar, Vinita Awalkanthe, Nilambari Sardeshmukh, Bhagyashree Sardeshmukh, Dhananjay Deshpande, Anjali Deshpande, Sandeep Chavan

Ovarian cancer patients with BRCA1 mutation have more susceptibility for secondary breast cancer. In females with BRCA1 mutation, the risk of developing breast carcinoma is 65% and of ovarian cancer is 39%, before 70 years of age. This is a case report of a 74 year old, post-menopausal woman diagnosed with metastatic retroperitoneal lymph node, high-grade papillary adenocarcinoma primary ovary stage IIIA in April 2004 at the age of 48 years. She underwent 3 cycles of neo-adjuvant chemotherapy Inj. Methotrexate and Inj. Carboplatin from June to August 2004 followed by optimum cytoreduction in September 2004. Later she completed 3 more cycles of chemotherapy of the same protocol from October to November 2004. Tab Etoposide was given from December 2004 to October 2006. In May 2006, during oral chemotherapy and with unremarkable radiological findings, the patient chose Ayurvedic treatment in view of immune boosting, and improving quality of life. The patient underwent 11 sets of Panchakarma treatment, almost every year, from December 2007 to September 2019. She was disease-free for 13 years leading a good quality of life with adjunct Ayurvedic treatment. In October 2019, she was diagnosed with Left breast duct carcinoma with ER, PR hormone positive status. Her genetic mutation analysis report at that time revealed BRCA 1 mutation. She underwent Left Modified Radical Mastectomy in October 2019, followed by prophylactic Right Breast Mastectomy and oral hormonal therapy. Now she is living with better quality of life with adjunct Ayurvedic treatment, including Oral Ayurvedic Medicines possessing Rasayana (immunomodulatory) and hepato-protective activity and 12 sets of Panchakarma Chikitsa. In this case of Stage IIIA Ovarian carcinoma and second primary Breast carcinoma with BRCA 1 genetic mutation (HBOC syndrome), a long-term 13 years of disease-free survival, and 20 years of overall survival is achieved with the integration of Ayurvedic treatment and conventional cancer treatment.

BRCA1突变的卵巢癌患者继发性乳腺癌易感性更高。在70岁之前,携带BRCA1突变的女性患乳腺癌的风险为65%,患卵巢癌的风险为39%。本文报告一例74岁绝经后妇女,2004年4月诊断为转移性腹膜后淋巴结,高级别乳头状腺癌原发性卵巢IIIA期,年龄48岁。新辅助化疗注射3个周期。甲氨蝶呤注射液。卡铂在2004年6月至8月,随后是2004年9月的最佳细胞减少。后来她在2004年10月到11月又完成了三个相同方案的化疗周期。Tab Etoposide于2004年12月至2006年10月使用。2006年5月,在口服化疗期间,鉴于增强免疫力和改善生活质量,患者选择了阿育吠陀治疗。从2007年12月到2019年9月,患者几乎每年接受11组Panchakarma治疗。13年来,她一直没有患病,在辅助的阿育吠陀治疗下,生活质量很好。2019年10月,她被诊断为左乳管癌,ER、PR激素阳性。她当时的基因突变分析报告显示为brca1突变。她于2019年10月接受了左侧改良根治性乳房切除术,随后接受了预防性右侧乳房切除术和口服激素治疗。现在,通过辅助的阿育吠陀治疗,她的生活质量得到了提高,包括具有免疫调节和肝保护活性的口服阿育吠陀药物和12套Panchakarma Chikitsa。在本例IIIA期卵巢癌和第二原发性乳腺癌合并brca1基因突变(HBOC综合征)的病例中,阿育吠陀治疗与常规癌症治疗相结合,实现了13年的长期无病生存期和20年的总生存期。
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引用次数: 0
Evaluating anticancer potentials of potentized preparations in an in-vivo xenograft model. 在体内异种移植模型中评估增强制剂的抗癌潜力。
IF 1.7 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE Pub Date : 2024-11-01 Epub Date: 2024-12-02 DOI: 10.1016/j.jaim.2024.101015
Rajesh Shah, Gitanjali Talele, Nirmal Kumar Kasinathan, Madan Barkume, Jyoti Kode

Background: Xenografts in immunodeficient mice play a pivotal role in testing novel anti-cancer treatments. Xenograft models expedite the drug discovery process, offering a cost-effective alternative to conventional animal models and providing essential data for clinical trials. We have followed the approach described by the Developmental Therapeutics Program of the National Cancer Institute (NCI), USA to investigate the therapeutic responses.

Objectives: In this research, potentized preparations derived from biomaterial, referred to as nosodes, have exhibited promising effectiveness against cancer in laboratory experiments. This study seeks to further substantiate these findings by employing animal models.

Method: Potentized preparations from category nosodes sourced from biomaterials of HIV, Cancer tissue, Hepatitis C and a combination underwent testing within the NCI's preclinical evaluation protocols using Xenograft models (HOP62). All the experimental mice were randomly assigned to one of six groups (n = 6), including vehicle and positive controls. These preparations were administered orally at a dosage of 0.1 ml, five days a week, over a four-week period. The mice were closely monitored at regular intervals for 32 days, with observations regarding changes in body weight, tumor volume, morbidity, and mortality. Relative tumor volume (RTV) was calculated as the tumor volume on the day of measurement divided by the tumor volume on day 1.

Results: The groups treated with Hepatitis C 30c and HIV 100c nosodes have not shown effect with respect to Relative Tumor Volume (RTV). Evidence of significant tumor regression was observed for RTV on day 30 in groups treated with HIV nosode 30c (P = 0.002), and Cancer nosode 30c (P = 0.005). Percentage Survival was noted better in HIV nosode 30c treated group from day 25, however, in other groups survival percentage remained constant. Varied animal body weight in all groups was noted. Significant differences in tumor volume with respect to time in all treated groups were observed.

Conclusion: Results are suggestive of tumor regression which is encouraging to undertake further clinical trials to explore the anticancer potential of HIV nosode and Cancer nosode.

背景:免疫缺陷小鼠的异种移植物在检测新的抗癌治疗方法中起着关键作用。异种移植模型加快了药物发现过程,为传统动物模型提供了一种经济有效的替代方案,并为临床试验提供了必要的数据。我们遵循美国国家癌症研究所(NCI)的发展治疗计划所描述的方法来调查治疗反应。目的:在本研究中,从生物材料中提取的潜在制剂,被称为nosodes,在实验室实验中显示出抗癌的良好效果。本研究试图通过采用动物模型进一步证实这些发现。方法:在NCI的临床前评估方案中,使用异种移植模型(HOP62)对来自HIV、癌症组织、丙型肝炎及其组合生物材料的nosodes类别的增强制剂进行测试。所有实验小鼠随机分为6组(n = 6),包括对照组和阳性对照组。这些制剂以0.1 ml的剂量口服,每周五天,为期四周。定期监测小鼠32天,观察体重、肿瘤体积、发病率和死亡率的变化。相对肿瘤体积(Relative tumor volume, RTV)为测量当天的肿瘤体积除以第1天的肿瘤体积。结果:丙型肝炎30c和HIV 100c治疗组在相对肿瘤体积(RTV)方面没有显示出效果。使用HIV nosode 30c和Cancer nosode 30c治疗组的RTV在第30天有显著的肿瘤消退(P = 0.002)。从第25天开始,HIV nosode 30c治疗组的存活率更高,但其他组的存活率保持不变。各组动物体重差异显著。观察到所有治疗组的肿瘤体积相对于时间有显著差异。结论:结果提示肿瘤消退,值得开展进一步的临床试验,探索HIV和Cancer nosode的抗癌潜力。
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引用次数: 0
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Journal of Ayurveda and Integrative Medicine
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