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Myrislignan (MRL) existing in nutmeg has been reported to possess inhibition of neoplasm and vascular smooth muscle contraction, and cause a prolonging of hexobarbital-induced hypnosis in mice. In this study, a highperformance liquid chromatography-ultraviolet detection (HPLC-UV) method was developed to analyze MRL in rat tissues. The separation was carried out on an analytical Diamonsil TM ODS C 18 HPLC column (250 9 4.6 mm, 5 lm) equipped with a C 18 guard column (8 9 4 mm, 5 lm) cartridge system eluted at 1.0 mL min -1 with a mobile phase methanol-H 2 O (3:1, v/v). Detection wavelength was 270 nm. The concentration of MRL was analyzed in the brain, testes, muscle, adipose, kidney, heart, lung, stomach, intestine, liver, and spleen at various time points between 8 and 128 min following intravenous administration of MRL to rats at a dose of 20.0 mg kg -1 . The method was successfully used to study the tissue distribution of MRL. The results contribute to explain the effect of nutmeg on the brain, liver and gastrointestinal tract.
Myrislignan (MRL) existing in nutmeg has been reported to possess inhibition of neoplasm and vascular smooth muscle contraction, and cause a prolonging of hexobarbital-induced hypnosis in mice. In this study, a highperformance liquid chromatography-ultraviolet detection (HPLC-UV) method was developed to analyze MRL in rat tissues. The separation was carried out on an analytical Diamonsil TM ODS C 18 HPLC column (250 9 4.6 mm, 5 lm) equipped with a C 18 guard column (8 9 4 mm, 5 lm) cartridge system eluted at 1.0 mL min -1 with a mobile phase methanol-H 2 O (3:1, v/v). Detection wavelength was 270 nm. The concentration of MRL was analyzed in the brain, testes, muscle, adipose, kidney, heart, lung, stomach, intestine, liver, and spleen at various time points between 8 and 128 min following intravenous administration of MRL to rats at a dose of 20.0 mg kg -1 . The method was successfully used to study the tissue distribution of MRL. The results contribute to explain the effect of nutmeg on the brain, liver and gastrointestinal tract.
Background: Natural products are secondary metabolites obtained from plants, animals, and microorganisms with diverse chemical structures resulting in diverse biological functions and drug-like properties. Objective: This review article summarizes in detail the occurrence, detection, isolation, various pharmacological properties, metabolism, and toxicity of a natural compound i.e., 5-Allyl-1-methoxy-2,3-methylenedioxybenzene commonly known as Myristicin. Methods: A relevant literature search was made using the keywords essential oil, mace, myristicin, nutmeg, and pharmacological activities from different databases such as Pub Med, Sci finder, Science Direct, and Google Scholar. The literature search results presented articles from 1963 to 2022. Thereafter, the articles were carefully screened and selected for review. Results: Myristicin, an alkoxy-substituted allylbenzene is present in major to minor amounts in the essential oils obtained from different plant parts and exhibits various pharmacological properties such as antimicrobial, antioxidant, antiproliferative, anti-inflammatory, insecticidal, and hepatoprotective. It forms 10 metabolites by reduction, demethylation, hydroxylation, ring formation, ring-opening, and conjugate formation. In the liver, myristicin has been metabolized by Cytochrome P450 complex enzymes to generate active metabolite (1ˈ hyroxymyristicin) responsible for cytotoxic, genotoxic and apoptotic effects (150 µM). But, myristicin at 600 µM does not produce enough 1ʼ-hydroxymyristicin to give the final toxicant. Conclusion: Myristicin poses no major risk to human health through the consumption of herbs and spices due to its presence in low amounts. It has great potential to be used in the traditional system of medicine. We hope that this review will provide complete knowledge about myristicin on a single platform.
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