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We are analyzing https://link.springer.com/article/10.1007/s00210-023-02679-z.

Title:
Antitubercular drugs: possible role of natural products acting as antituberculosis medication in overcoming drug resistance and drug-induced hepatotoxicity | Naunyn-Schmiedeberg's Archives of Pharmacology
Description:
Mycobacterium tuberculosis (Mtb) is a pathogenic bacterium which causes tuberculosis (TB). TB control programmes are facing threats from drug resistance. Multidrug-resistant (MDR) and extensively drug-resistant (XDR) Mtb strains need longer and more expensive treatment with many medications resulting in more adverse effects and decreased chances of treatment outcomes. The World Health Organization (WHO) has emphasised the development of not just new individual anti-TB drugs, but also novel medication regimens as an alternative treatment option for the drug-resistant Mtb strains. Many plants, as well as marine creatures (sponge; Haliclona sp.) and fungi, have been continuously used to treat TB in various traditional treatment systems around the world, providing an almost limitless supply of active components. Natural products, in addition to their anti-mycobacterial action, can be used as adjuvant therapy to increase the efficacy of conventional anti-mycobacterial medications, reduce their side effects, and reverse MDR Mtb strain due to Mycobacterium’s genetic flexibility and environmental adaptation. Several natural compounds such as quercetin, ursolic acid, berberine, thymoquinone, curcumin, phloretin, and propolis have shown potential anti-mycobacterial efficacy and are still being explored in preclinical and clinical investigations for confirmation of their efficacy and safety as anti-TB medication. However, more high-level randomized clinical trials are desperately required. The current review provides an overview of drug-resistant TB along with the latest anti-TB medications, drug-induced hepatotoxicity and oxidative stress. Further, the role and mechanisms of action of first and second-line anti-TB drugs and new drugs have been highlighted. Finally, the role of natural compounds as anti-TB medication and hepatoprotectants have been described and their mechanisms discussed.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {📚}

  • Education
  • Science
  • Health & Fitness

Content Management System {📝}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {📈}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {💸}

We see no obvious way the site makes money.

The purpose of some websites isn't monetary gain; they're meant to inform, educate, or foster collaboration. Everyone has unique reasons for building websites. This could be an example. Link.springer.com has a secret sauce for making money, but we can't detect it yet.

Keywords {🔍}

article, pubmed, google, scholar, pmid, cas, tuberculosis, central, mycobacterium, resistance, agents, zhang, wang, kumar, drug, med, httpsdoiorg, antimicrob, chemother, natural, httpsdoiorgaac, pandey, httpsdoiorgs, liu, drugs, products, review, treatment, kim, activity, hepatotoxicity, role, singh, antituberculosis, mechanisms, chem, action, clinical, liver, sci, drugresistant, antimycobacterial, potential, oxidative, stress, chen, isoniazid, van, lee, microbiol,

Topics {✒️}

int/publications/digital/global-tuberculosis-report-2021/tb-diagnosis-treatment/drug-resistant-treatment wijaya month download article/chapter decaprenylphosphoryl-β-d-arabinose biosynthetic nitroimidazole-oxazine-specific protein involved high-level ethambutol-resistant tuberculosis drug-induced liver injury multi-omics integration reveals anti-tuberculosis therapy-induced hepatotoxicity extensively drug-resistant tuberculosis long-term lipid diet nitro-dihydro-imidazooxazole derivative anti-mycobacterial natural products small-moleculenitroimidazopyran drug candidate drug-resistant mtb strains drug-induced liver toxicity exploring anti-tb leads enrich lung-resident memory acknowledges research associateship drug para-aminosalicylic acid selected medicinal plants conventional anti-mycobacterial medications multidrug-resistant pulmonary tuberculosis atds-induced hepatic damage hei-oc1 auditory cells d-cycloserine resistance trait difficult multidrug-resistant tuberculosis open chemistry 19 fluoroquinolone-resistant mycobacterium tuberculosis drug-resistant mycobacterium tuberculosis cisplatin-induced oxidative stress potential anti-tubercular leads alloxan-induced diabetic rats individual anti-tb drugs article naunyn-schmiedeberg' quercetin 3-o-glucoside recovered latest anti-tb medications line anti-tb drugs accepted manuscript version multidrug-resistant mycobacterium tuberculosis structure–microbicidal activity relationship extensively drug-resistant vitro anti-mycobacterial activity full article pdf unique c-terminal extension line anti-tuberculosis drugs pyrazinamide inhibits trans-translation global chemical composition drug-resistant strains antitubercular drugs-induced hepatotoxicity drug-resistant tb

Questions {❓}

  • Field SK (2015) Bedaquiline for the treatment of multidrug-resistant tuberculosis: great promise or disappointment?

Schema {🗺️}

WebPage:
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         headline:Antitubercular drugs: possible role of natural products acting as antituberculosis medication in overcoming drug resistance and drug-induced hepatotoxicity
         description: Mycobacterium tuberculosis (Mtb) is a pathogenic bacterium which causes tuberculosis (TB). TB control programmes are facing threats from drug resistance. Multidrug-resistant (MDR) and extensively drug-resistant (XDR) Mtb strains need longer and more expensive treatment with many medications resulting in more adverse effects and decreased chances of treatment outcomes. The World Health Organization (WHO) has emphasised the development of not just new individual anti-TB drugs, but also novel medication regimens as an alternative treatment option for the drug-resistant Mtb strains. Many plants, as well as marine creatures (sponge; Haliclona sp.) and fungi, have been continuously used to treat TB in various traditional treatment systems around the world, providing an almost limitless supply of active components. Natural products, in addition to their anti-mycobacterial action, can be used as adjuvant therapy to increase the efficacy of conventional anti-mycobacterial medications, reduce their side effects, and reverse MDR Mtb strain due to Mycobacterium’s genetic flexibility and environmental adaptation. Several natural compounds such as quercetin, ursolic acid, berberine, thymoquinone, curcumin, phloretin, and propolis have shown potential anti-mycobacterial efficacy and are still being explored in preclinical and clinical investigations for confirmation of their efficacy and safety as anti-TB medication. However, more high-level randomized clinical trials are desperately required. The current review provides an overview of drug-resistant TB along with the latest anti-TB medications, drug-induced hepatotoxicity and oxidative stress. Further, the role and mechanisms of action of first and second-line anti-TB drugs and new drugs have been highlighted. Finally, the role of natural compounds as anti-TB medication and hepatoprotectants have been described and their mechanisms discussed.
         datePublished:2023-09-04T00:00:00Z
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      headline:Antitubercular drugs: possible role of natural products acting as antituberculosis medication in overcoming drug resistance and drug-induced hepatotoxicity
      description: Mycobacterium tuberculosis (Mtb) is a pathogenic bacterium which causes tuberculosis (TB). TB control programmes are facing threats from drug resistance. Multidrug-resistant (MDR) and extensively drug-resistant (XDR) Mtb strains need longer and more expensive treatment with many medications resulting in more adverse effects and decreased chances of treatment outcomes. The World Health Organization (WHO) has emphasised the development of not just new individual anti-TB drugs, but also novel medication regimens as an alternative treatment option for the drug-resistant Mtb strains. Many plants, as well as marine creatures (sponge; Haliclona sp.) and fungi, have been continuously used to treat TB in various traditional treatment systems around the world, providing an almost limitless supply of active components. Natural products, in addition to their anti-mycobacterial action, can be used as adjuvant therapy to increase the efficacy of conventional anti-mycobacterial medications, reduce their side effects, and reverse MDR Mtb strain due to Mycobacterium’s genetic flexibility and environmental adaptation. Several natural compounds such as quercetin, ursolic acid, berberine, thymoquinone, curcumin, phloretin, and propolis have shown potential anti-mycobacterial efficacy and are still being explored in preclinical and clinical investigations for confirmation of their efficacy and safety as anti-TB medication. However, more high-level randomized clinical trials are desperately required. The current review provides an overview of drug-resistant TB along with the latest anti-TB medications, drug-induced hepatotoxicity and oxidative stress. Further, the role and mechanisms of action of first and second-line anti-TB drugs and new drugs have been highlighted. Finally, the role of natural compounds as anti-TB medication and hepatoprotectants have been described and their mechanisms discussed.
      datePublished:2023-09-04T00:00:00Z
      dateModified:2023-09-04T00:00:00Z
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         Tuberculosis
         Drug-resistance
         Hepatoprotective
         Natural products
         Liver injury
         Pharmacology/Toxicology
         Neurosciences
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            name:Ramesh Kumar
            affiliation:
                  name:University of Allahabad
                  address:
                     name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
                     type:PostalAddress
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                  name:Central University of Punjab
                  address:
                     name:Department of Biochemistry, Central University of Punjab, Bathinda, India
                     type:PostalAddress
                  type:Organization
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            name:Abhay K. Pandey
            affiliation:
                  name:University of Allahabad
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      address:
         name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
         type:PostalAddress
      name:BMK Government. Girls College
      address:
         name:Department of Botany, BMK Government. Girls College, Balod, India
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      address:
         name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
         type:PostalAddress
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      address:
         name:Department of Biochemistry, Central University of Punjab, Bathinda, India
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      address:
         name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
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            address:
               name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
               type:PostalAddress
            type:Organization
            name:Feroze Gandhi College
            address:
               name:Department of Zoology, Feroze Gandhi College, Raebareli, India
               type:PostalAddress
            type:Organization
      name:Amit Kumar Singh
      affiliation:
            name:University of Allahabad
            address:
               name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
               type:PostalAddress
            type:Organization
            name:BMK Government. Girls College
            address:
               name:Department of Botany, BMK Government. Girls College, Balod, India
               type:PostalAddress
            type:Organization
      name:Ramesh Kumar
      affiliation:
            name:University of Allahabad
            address:
               name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
               type:PostalAddress
            type:Organization
            name:Central University of Punjab
            address:
               name:Department of Biochemistry, Central University of Punjab, Bathinda, India
               type:PostalAddress
            type:Organization
      name:Abhay K. Pandey
      affiliation:
            name:University of Allahabad
            address:
               name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
               type:PostalAddress
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      name:Department of Botany, BMK Government. Girls College, Balod, India
      name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
      name:Department of Biochemistry, Central University of Punjab, Bathinda, India
      name:Department of Biochemistry, University of Allahabad, Prayagraj (Allahabad), India
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