Comparison of treatment of COVID-19 with inhaled bromhexine, higher doses of colchicine and hymecromone with WHO-recommended paxlovid, molnupiravir, remdesivir, anti-IL-6 receptor antibodies and baricitinib

IF 1.1 Q4 PHARMACOLOGY & PHARMACY
Vanyo Mitev
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引用次数: 1

Abstract

Millions of publications and thousands of clinical trials have not led to the discovery of an effective treatment for COVID-19. We believe that the reason for this is the inaccurate strategy of inhibiting target molecules involved in the pathogenesis of the disease. The leading cause of death in COVID-19 is the cytokine storm, which is caused by an NLRP3 inflammasome hyperreaction. WHO recommends for the outpatients treatment drugs blocking the replication of SARS-CoV-2. However, viral load and replication are not directly related to NLRP3 inflammasome hyperreactivity. This also explains the partial success of the WHO favorite paxlovid to reduce hospitalizations (51%). For hospital treatment, WHO suggests antibodies against the interleukin-6 receptor and Janus kinase (JAK) inhibition. Although important, IL-6 is one of dozens of cytokines elevated as a consequence of cytokine storm. The JAK inhibitor baricitinib inhibited the effect of not only IL-6 but also other elevated cytokines. But if the NLRP3 inflammasome is inhibited, the cytokines will not be elevated, and there will be no need for baricitinib. All medicines recommended by the WHO are distinguished by their very high prices. Our therapeutic strategy is based on inhibition of SARS-CoV-2 entry into the cell and inhibition of the NLRP3 inflammasome. We offer two readily available, cheap and well-known medications - bromhexine hydrochloride and colchicine. The many studies on the treatment of COVID-19 so far have not produced the expected result. The devil is buried in the details. For bromhexine, the reason is the way and its late application. Bromhexine is most effective when given prophylactically or started by inhalation after contact with a person with COVID-19. Its earliest possible application is crucial for its effect. Increased doses of colchicine are necessary for COVID-19 treatment due to the fact that it accumulates in leukocytes, and this leads to inhibition of NLRP3. The high doses we administer have been given widely in the past and are completely safe. Our highest dose is about 5 times lower per kg of weight than the lowest severe toxic dose of colchicine described. Our results show about a 5-fold decrease in hospital mortality and almost complete prevention of hospitalizations if outpatients are treated with inhaled bromhexine and colchicine.
Comparison与世卫组织推荐的paxlovid、molnupiravir、remdesivir、抗il -6受体抗体和baricitinib联合使用高剂量秋水仙碱和羟色酮治疗COVID-19的疗效
数以百万计的出版物和成千上万的临床试验都没有发现COVID-19的有效治疗方法。我们认为,造成这种情况的原因是抑制参与疾病发病机制的靶分子的策略不准确。COVID-19的主要死亡原因是细胞因子风暴,这是由NLRP3炎症小体过度反应引起的。世卫组织建议将阻断新冠病毒复制的药物用于门诊治疗。然而,病毒载量和复制与NLRP3炎性体的高反应性没有直接关系。这也解释了世卫组织最喜欢的paxlovid在减少住院率(51%)方面部分成功的原因。对于医院治疗,世卫组织建议使用针对白细胞介素-6受体的抗体和Janus激酶(JAK)抑制。尽管IL-6很重要,但它是细胞因子风暴导致的数十种细胞因子升高之一。JAK抑制剂baricitinib不仅抑制IL-6的作用,还抑制其他升高的细胞因子的作用。但如果NLRP3炎性体受到抑制,细胞因子就不会升高,也就不需要巴西替尼了。世卫组织推荐的所有药物的特点是价格非常高。我们的治疗策略是基于抑制SARS-CoV-2进入细胞和抑制NLRP3炎症小体。我们提供两种现成的、便宜的、众所周知的药物——盐酸溴己辛和秋水仙碱。迄今为止,许多关于新冠肺炎治疗的研究并没有产生预期的结果。细节决定成败。溴化辛的原因在于方法和应用较晚。溴甲基辛在预防性服用或与COVID-19患者接触后吸入时最有效。尽早应用对其效果至关重要。秋水仙碱在白细胞中积累,导致NLRP3抑制,因此需要增加秋水仙碱的剂量来治疗COVID-19。我们使用的高剂量疫苗在过去被广泛使用,而且是完全安全的。我们的最高剂量每公斤体重比秋水仙碱的最低严重毒性剂量低约5倍。我们的研究结果显示,如果门诊病人吸入溴化氢和秋水仙碱治疗,住院死亡率降低约5倍,几乎完全预防住院。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmacia
Pharmacia PHARMACOLOGY & PHARMACY-
CiteScore
2.30
自引率
27.30%
发文量
114
审稿时长
12 weeks
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