The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analogues

Mycotoxin MT81 isolated from Penicillium nigricans and its two structural derivatives viz. Acetylated MT81 (AcMT81) and Benzoylated MT81 (BzMT81) show antimicrobial activities as well as cause hepatotoxicity and nephrotoxicity. Present study deals with the CNS depressant activity of the above said t...

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Main Author: Sujata Maiti Choudhury
Format: Article
Language:English
Published: Al Ameen Medical College 2008-12-01
Series:Al Ameen Journal of Medical Sciences
Subjects:
Online Access:http://ajms.alameenmedical.org/articel_vol2/AJMS.2.P-104-114-C.pdf
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spelling doaj-8ee90bd9a81d43ccb95bd5be22e2f2f32020-11-25T01:52:31ZengAl Ameen Medical CollegeAl Ameen Journal of Medical Sciences0974-11432008-12-010102104114The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analoguesSujata Maiti ChoudhuryMycotoxin MT81 isolated from Penicillium nigricans and its two structural derivatives viz. Acetylated MT81 (AcMT81) and Benzoylated MT81 (BzMT81) show antimicrobial activities as well as cause hepatotoxicity and nephrotoxicity. Present study deals with the CNS depressant activity of the above said toxins. Sedative-hypnotic and hypothermic actions were assessed by injecting MT81, AcMT81, and BzMT81 at three different doses prior to the administration of diazepam, chloropromazine and pentobarbitone respectively. The analgesic actions were studied by hot plate method. The sleep induced by diazepam, chlorpromazine and pentobarbitone were prolonged following the administration of MT81, AcMT81 and BzMT81. Significant hypothermia produced in a dose-dependent manner after the treatment with MT81 and its two derivatives. The toxins also potentiated the analgesic action of morphine significantly (p≤0.001). Being less toxic than the parent toxin MT81, the structural analogues showed more prominent analgesic activities, sedative effects and hypothermic actions.http://ajms.alameenmedical.org/articel_vol2/AJMS.2.P-104-114-C.pdfCNS depressant activitySedativeHypnoticHypothermicAnalgesic
collection DOAJ
language English
format Article
sources DOAJ
author Sujata Maiti Choudhury
spellingShingle Sujata Maiti Choudhury
The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analogues
Al Ameen Journal of Medical Sciences
CNS depressant activity
Sedative
Hypnotic
Hypothermic
Analgesic
author_facet Sujata Maiti Choudhury
author_sort Sujata Maiti Choudhury
title The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analogues
title_short The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analogues
title_full The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analogues
title_fullStr The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analogues
title_full_unstemmed The central nervous system depressant activities of Mycotoxin MT81 and its Acetylated and Benzoylated analogues
title_sort central nervous system depressant activities of mycotoxin mt81 and its acetylated and benzoylated analogues
publisher Al Ameen Medical College
series Al Ameen Journal of Medical Sciences
issn 0974-1143
publishDate 2008-12-01
description Mycotoxin MT81 isolated from Penicillium nigricans and its two structural derivatives viz. Acetylated MT81 (AcMT81) and Benzoylated MT81 (BzMT81) show antimicrobial activities as well as cause hepatotoxicity and nephrotoxicity. Present study deals with the CNS depressant activity of the above said toxins. Sedative-hypnotic and hypothermic actions were assessed by injecting MT81, AcMT81, and BzMT81 at three different doses prior to the administration of diazepam, chloropromazine and pentobarbitone respectively. The analgesic actions were studied by hot plate method. The sleep induced by diazepam, chlorpromazine and pentobarbitone were prolonged following the administration of MT81, AcMT81 and BzMT81. Significant hypothermia produced in a dose-dependent manner after the treatment with MT81 and its two derivatives. The toxins also potentiated the analgesic action of morphine significantly (p≤0.001). Being less toxic than the parent toxin MT81, the structural analogues showed more prominent analgesic activities, sedative effects and hypothermic actions.
topic CNS depressant activity
Sedative
Hypnotic
Hypothermic
Analgesic
url http://ajms.alameenmedical.org/articel_vol2/AJMS.2.P-104-114-C.pdf
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