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    <timestamp>20240115140420000</timestamp>
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      <depositor_name>Editor</depositor_name>
      <email_address>editor.jddt@gmail.com</email_address>
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    <registrant>Universal Journal of Pharmaceutical Research</registrant>
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        <full_title>Universal Journal of Pharmaceutical Research</full_title>
        <abbrev_title>Univ J Pharm Res</abbrev_title>
        <issn media_type="electronic">2456-8058</issn>
        <issn media_type="print">2831-5235</issn>
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        <publication_date media_type="online">
          <month>01</month>
          <day>15</day>
          <year>2024</year>
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          <title>ACUTE TOXICITY AND HEPATO-RENAL PROTECTION OF LIME JUICE, HONEY AND THEIR FLAVONOID-RICH FRACTIONS IN HIGH FAT-DIET INDUCED OBESE RAT MODEL</title>
        </titles>
        <contributors>
          <person_name contributor_role="author" sequence="first" language="en">
            <given_name>Idoko</given_name>
            <surname>Alexander</surname>
            <ORCID>https://orcid.org/0000-0001-7969-1489</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Parker Joshua</given_name>
            <surname>Elijah</surname>
            <ORCID>https://orcid.org/0000-0002-9671-4977</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Njoku Obioma</given_name>
            <surname>Uzoma</surname>
            <ORCID>https://orcid.org/0000-0001-6589-2263</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Ejike David</given_name>
            <surname>Ifeanyi</surname>
            <ORCID>https://orcid.org/0009-0007-2629-339X</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Egbuji Jude</given_name>
            <surname>Victor</surname>
            <ORCID>https://orcid.org/0000-0003-4358-052X</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Ugwudike</given_name>
            <surname>Patrick O</surname>
            <ORCID>https://orcid.org/0000-0002-9595-5242</ORCID>
          </person_name>
          <person_name contributor_role="author" sequence="additional" language="en">
            <given_name>Jennifer Ndubuisi</given_name>
            <surname>Chioma</surname>
            <ORCID>https://orcid.org/0009-0008-1888-2239</ORCID>
          </person_name>
        </contributors>
        <jats:abstract xmlns:jats="http://www.ncbi.nlm.nih.gov/JATS1">
          <jats:p>Introduction: A major consideration for the use of alternative herbal medicine from natural compounds is the concern of safety due to possible toxicity. This study evaluated the safety and hepato-renal protection of fresh lime juice (FLJ), raw honey (RH) and their flavonoid-rich fractions in obese rat induced high fat-diet (HFD).
Methods: Oral acute toxicity (LD50) study involved 24 female Wistar rats, divided into 8 groups of 3 rats, administered 300 mg/kg and 2000 mg/kg of FLJ, RH, methanol flavonoid rich fraction of lime juice (MFLJ) and ethyl acetate flavonoid rich fraction of honey (EAFH) respectively, for 14 days. Simultaneously, for the anti-obesity study, 24 neonate Wistar rats of 21-days old, divided into 2 groups of 12 rats (for obesity induction phase-1, for two weeks), and regrouped into 4 groups of 4 rats (14 days treatment phase-2), were used.
Results: Result of LD50 on FLJ, RH, MFLJ, and EAFH showed no toxicity, no motility, and body weight of rats was not adversely affected evenup to 2000 mg/kg.The increased body weight of the HFD-obese rats was significantly (p&lt;0.05)reduced compared to control. There was significant (p&lt;0.05) decrease in activities of aspartate aminotransferase and alanine aminotransferase after MIX, MFLJ and EAFH administration, compared with control. Also, total protein and bilirubin concentrations was not significantly (p&lt;0.05) different compared to control. Administration of EAFH significantly (p&lt;0.05) reduced the concentrations of creatinine, urea, potassium, and chloride; while MIX and EAFH significantly (p&lt;0.05) increased their concentrations compared to control.
Conclusion: It may be concluded that FLJ, RH, MFLJ, and EAFH are safe for consumption and also possess liver and renal protection.
                  
Peer Review History: 
Received: 27 October 2023; Revised: 19 November; Accepted: 28 December, Available online: 15 January 2024
Academic Editor: Dr. Asia Selman Abdullah, Pharmacy institute, University of Basrah, Iraq, asia_abdullah65@yahoo.com
Received file:                             Reviewer's Comments:
Average Peer review marks at initial stage: 6.0/10
Average Peer review marks at publication stage: 7.5/10
Reviewers:
Ahmad Najib, Universitas Muslim Indonesia, Makassar, Indonesia, ahmad.najib@umi.ac.id
Dr. Sangeetha Arullappan, Universiti Tunku Abdul Rahman, Malaysia, sangeetha@utar.edu.my
Dr. Gehan Fawzy Abdel Raoof Kandeel, Pharmacognosy Department, National Research Centre, Dokki, 12622,  Giza, Egypt, gehankandeel9@yahoo.com </jats:p>
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          <month>01</month>
          <day>15</day>
          <year>2024</year>
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