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Safety and Efficacy of Jenacid® Herbal Product Against Indomethacin-Induced Ulcers in Albino Wistar Rats
Jenacid Herbal Product (JHP) used for treating peptic ulcer disease in Uganda, sold over the counter, is approved by the National Drug Authority as a Traditional Herbal Product number THP 482. There have been no published studies on its safety and efficacy. This study aimed to assess potential acute...
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Published in: | Curēus (Palo Alto, CA) CA), 2024-10, Vol.16 (10), p.e72606 |
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description | Jenacid Herbal Product (JHP) used for treating peptic ulcer disease in Uganda, sold over the counter, is approved by the National Drug Authority as a Traditional Herbal Product number THP 482. There have been no published studies on its safety and efficacy.
This study aimed to assess potential acute and subacute toxicity as well as the efficacy of JHP.
An acute toxicity test was performed on Swiss Albino Wistar rats using Lorke's method at single oral doses of 10-5000 mg/kg. General change in behavior, adverse effects, and mortality were determined. In the subacute study, Wistar rats received daily oral doses of 250, 500, and 1000 mg/kg of JHP for 28 days. Body weight and biochemical and hematological parameters were measured at the end of the experiment. For the efficacy study, rats were randomly grouped into six groups (n=5). Gastric ulceration induced with a single oral dose of indomethacin 25 mg/kg. One group was humanely sacrificed under halothane anesthesia to confirm ulceration. Treatments included distilled water (negative control), 20 mg/kg omeprazole (positive control), 250, 500, and 1000 mg/kg of JHP for seven days, after which animals were sacrificed, stomachs excised out, observed for gastric lesions (number and severity), and scored.
The acute toxicity study showed oral LD50 of JHP was above 5000 mg/kg. A subacute toxicity study of JHP had no observable toxicity symptoms or significant variation in body weight, food and water consumption, hematological parameters, or mortality. Elevated aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were noted at 1000 mg/kg but within normal ranges. A significant decrease in total protein was observed at 500 mg/kg and 1000 mg/kg. JHP demonstrated ulcer-healing properties, with the highest efficacy at 500 mg/kg.
JHP is effective against ulcers with no significant adverse effects. However, chronic use of very high doses may cause a reduction in total protein levels. |
doi_str_mv | 10.7759/cureus.72606 |
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This study aimed to assess potential acute and subacute toxicity as well as the efficacy of JHP.
An acute toxicity test was performed on Swiss Albino Wistar rats using Lorke's method at single oral doses of 10-5000 mg/kg. General change in behavior, adverse effects, and mortality were determined. In the subacute study, Wistar rats received daily oral doses of 250, 500, and 1000 mg/kg of JHP for 28 days. Body weight and biochemical and hematological parameters were measured at the end of the experiment. For the efficacy study, rats were randomly grouped into six groups (n=5). Gastric ulceration induced with a single oral dose of indomethacin 25 mg/kg. One group was humanely sacrificed under halothane anesthesia to confirm ulceration. Treatments included distilled water (negative control), 20 mg/kg omeprazole (positive control), 250, 500, and 1000 mg/kg of JHP for seven days, after which animals were sacrificed, stomachs excised out, observed for gastric lesions (number and severity), and scored.
The acute toxicity study showed oral LD50 of JHP was above 5000 mg/kg. A subacute toxicity study of JHP had no observable toxicity symptoms or significant variation in body weight, food and water consumption, hematological parameters, or mortality. Elevated aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were noted at 1000 mg/kg but within normal ranges. A significant decrease in total protein was observed at 500 mg/kg and 1000 mg/kg. JHP demonstrated ulcer-healing properties, with the highest efficacy at 500 mg/kg.
JHP is effective against ulcers with no significant adverse effects. However, chronic use of very high doses may cause a reduction in total protein levels.</description><identifier>ISSN: 2168-8184</identifier><identifier>EISSN: 2168-8184</identifier><identifier>DOI: 10.7759/cureus.72606</identifier><identifier>PMID: 39610642</identifier><language>eng</language><publisher>United States: Cureus Inc</publisher><subject>Albinism ; Drug dosages ; Drug interactions ; Flavonoids ; Gastroenterology ; Herbal medicine ; Hydrochloric acid ; Infections ; Laboratory animals ; Oils & fats ; Pharmaceuticals ; Phytochemicals ; Side effects ; Sterols ; Toxicity ; Ulcers</subject><ispartof>Curēus (Palo Alto, CA), 2024-10, Vol.16 (10), p.e72606</ispartof><rights>Copyright © 2024, Kiprotich et al.</rights><rights>Copyright © 2024, Kiprotich et al. This work is published under https://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2024, Kiprotich et al. 2024 Kiprotich et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2156-f3c69b2c8f98935f4bb19eab97e4c4e1203cbb04d2fad70f1a149ae2355bc2c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3134454639/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3134454639?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39610642$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kiprotich, Joshua</creatorcontrib><creatorcontrib>Timothy, Neeza</creatorcontrib><creatorcontrib>Yadesa, Tadele M</creatorcontrib><creatorcontrib>Mwandah, Daniel C</creatorcontrib><title>Safety and Efficacy of Jenacid® Herbal Product Against Indomethacin-Induced Ulcers in Albino Wistar Rats</title><title>Curēus (Palo Alto, CA)</title><addtitle>Cureus</addtitle><description>Jenacid Herbal Product (JHP) used for treating peptic ulcer disease in Uganda, sold over the counter, is approved by the National Drug Authority as a Traditional Herbal Product number THP 482. There have been no published studies on its safety and efficacy.
This study aimed to assess potential acute and subacute toxicity as well as the efficacy of JHP.
An acute toxicity test was performed on Swiss Albino Wistar rats using Lorke's method at single oral doses of 10-5000 mg/kg. General change in behavior, adverse effects, and mortality were determined. In the subacute study, Wistar rats received daily oral doses of 250, 500, and 1000 mg/kg of JHP for 28 days. Body weight and biochemical and hematological parameters were measured at the end of the experiment. For the efficacy study, rats were randomly grouped into six groups (n=5). Gastric ulceration induced with a single oral dose of indomethacin 25 mg/kg. One group was humanely sacrificed under halothane anesthesia to confirm ulceration. Treatments included distilled water (negative control), 20 mg/kg omeprazole (positive control), 250, 500, and 1000 mg/kg of JHP for seven days, after which animals were sacrificed, stomachs excised out, observed for gastric lesions (number and severity), and scored.
The acute toxicity study showed oral LD50 of JHP was above 5000 mg/kg. A subacute toxicity study of JHP had no observable toxicity symptoms or significant variation in body weight, food and water consumption, hematological parameters, or mortality. Elevated aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were noted at 1000 mg/kg but within normal ranges. A significant decrease in total protein was observed at 500 mg/kg and 1000 mg/kg. JHP demonstrated ulcer-healing properties, with the highest efficacy at 500 mg/kg.
JHP is effective against ulcers with no significant adverse effects. However, chronic use of very high doses may cause a reduction in total protein levels.</description><subject>Albinism</subject><subject>Drug dosages</subject><subject>Drug interactions</subject><subject>Flavonoids</subject><subject>Gastroenterology</subject><subject>Herbal medicine</subject><subject>Hydrochloric acid</subject><subject>Infections</subject><subject>Laboratory animals</subject><subject>Oils & fats</subject><subject>Pharmaceuticals</subject><subject>Phytochemicals</subject><subject>Side effects</subject><subject>Sterols</subject><subject>Toxicity</subject><subject>Ulcers</subject><issn>2168-8184</issn><issn>2168-8184</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkd9qFTEQh4MottTeeS0Bb7zo1vzb7OZKDqW2lYKiFi_DJDtpU_YkNdkVzkv5ED5Ztz21VK9mhvn4McNHyGvODruuNe_9XHCuh53QTD8ju4Lrvul5r54_6XfIfq3XjDHOOsE69pLsSKM500rskvgNAk4bCmmgxyFED35Dc6CfMIGPw5_f9BSLg5F-KXmY_URXlxBTnehZGvIap6uFSs0yzB4HejF6LJXGRFejiynTH7FOUOhXmOor8iLAWHH_oe6Ri4_H349Om_PPJ2dHq_PGC97qJkivjRO-D6Y3sg3KOW4QnOlQeYVcMOmdY2oQAYaOBQ5cGUAh29Z54YXcIx-2uTezW-PgMU0FRntT4hrKxmaI9t9Nilf2Mv-ynGsmRauWhHcPCSX_nLFOdh2rx3GEhHmuVnKpmO41Nwv69j_0Os8lLf_dU6pVWt5RB1vKl1xrwfB4DWf2zqPderT3Hhf8zdMPHuG_1uQt1IObTg</recordid><startdate>20241029</startdate><enddate>20241029</enddate><creator>Kiprotich, Joshua</creator><creator>Timothy, Neeza</creator><creator>Yadesa, Tadele M</creator><creator>Mwandah, Daniel C</creator><general>Cureus Inc</general><general>Cureus</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20241029</creationdate><title>Safety and Efficacy of Jenacid® Herbal Product Against Indomethacin-Induced Ulcers in Albino Wistar Rats</title><author>Kiprotich, Joshua ; Timothy, Neeza ; Yadesa, Tadele M ; Mwandah, Daniel C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2156-f3c69b2c8f98935f4bb19eab97e4c4e1203cbb04d2fad70f1a149ae2355bc2c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Albinism</topic><topic>Drug dosages</topic><topic>Drug interactions</topic><topic>Flavonoids</topic><topic>Gastroenterology</topic><topic>Herbal medicine</topic><topic>Hydrochloric acid</topic><topic>Infections</topic><topic>Laboratory animals</topic><topic>Oils & fats</topic><topic>Pharmaceuticals</topic><topic>Phytochemicals</topic><topic>Side effects</topic><topic>Sterols</topic><topic>Toxicity</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kiprotich, Joshua</creatorcontrib><creatorcontrib>Timothy, Neeza</creatorcontrib><creatorcontrib>Yadesa, Tadele M</creatorcontrib><creatorcontrib>Mwandah, Daniel C</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Curēus (Palo Alto, CA)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kiprotich, Joshua</au><au>Timothy, Neeza</au><au>Yadesa, Tadele M</au><au>Mwandah, Daniel C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety and Efficacy of Jenacid® Herbal Product Against Indomethacin-Induced Ulcers in Albino Wistar Rats</atitle><jtitle>Curēus (Palo Alto, CA)</jtitle><addtitle>Cureus</addtitle><date>2024-10-29</date><risdate>2024</risdate><volume>16</volume><issue>10</issue><spage>e72606</spage><pages>e72606-</pages><issn>2168-8184</issn><eissn>2168-8184</eissn><abstract>Jenacid Herbal Product (JHP) used for treating peptic ulcer disease in Uganda, sold over the counter, is approved by the National Drug Authority as a Traditional Herbal Product number THP 482. There have been no published studies on its safety and efficacy.
This study aimed to assess potential acute and subacute toxicity as well as the efficacy of JHP.
An acute toxicity test was performed on Swiss Albino Wistar rats using Lorke's method at single oral doses of 10-5000 mg/kg. General change in behavior, adverse effects, and mortality were determined. In the subacute study, Wistar rats received daily oral doses of 250, 500, and 1000 mg/kg of JHP for 28 days. Body weight and biochemical and hematological parameters were measured at the end of the experiment. For the efficacy study, rats were randomly grouped into six groups (n=5). Gastric ulceration induced with a single oral dose of indomethacin 25 mg/kg. One group was humanely sacrificed under halothane anesthesia to confirm ulceration. Treatments included distilled water (negative control), 20 mg/kg omeprazole (positive control), 250, 500, and 1000 mg/kg of JHP for seven days, after which animals were sacrificed, stomachs excised out, observed for gastric lesions (number and severity), and scored.
The acute toxicity study showed oral LD50 of JHP was above 5000 mg/kg. A subacute toxicity study of JHP had no observable toxicity symptoms or significant variation in body weight, food and water consumption, hematological parameters, or mortality. Elevated aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were noted at 1000 mg/kg but within normal ranges. A significant decrease in total protein was observed at 500 mg/kg and 1000 mg/kg. JHP demonstrated ulcer-healing properties, with the highest efficacy at 500 mg/kg.
JHP is effective against ulcers with no significant adverse effects. However, chronic use of very high doses may cause a reduction in total protein levels.</abstract><cop>United States</cop><pub>Cureus Inc</pub><pmid>39610642</pmid><doi>10.7759/cureus.72606</doi><oa>free_for_read</oa></addata></record> |
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subjects | Albinism Drug dosages Drug interactions Flavonoids Gastroenterology Herbal medicine Hydrochloric acid Infections Laboratory animals Oils & fats Pharmaceuticals Phytochemicals Side effects Sterols Toxicity Ulcers |
title | Safety and Efficacy of Jenacid® Herbal Product Against Indomethacin-Induced Ulcers in Albino Wistar Rats |
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