Sofía Padilla-Mayne, Berenice Ovalle-Magallanes, Mario Figueroa*, Edelmira Linares, Robert Bye, Isabel Rivero-Cruz, Martín González-Andrade, Rodrigo Aguayo-Ortiz and Rachel Mata*,
{"title":"Chemical Analysis and Antidiabetic Potential of a Decoction from Stevia serrata Roots","authors":"Sofía Padilla-Mayne, Berenice Ovalle-Magallanes, Mario Figueroa*, Edelmira Linares, Robert Bye, Isabel Rivero-Cruz, Martín González-Andrade, Rodrigo Aguayo-Ortiz and Rachel Mata*, ","doi":"10.1021/acs.jnatprod.3c00711","DOIUrl":null,"url":null,"abstract":"<p >A decoction of the roots (31.6–316 mg/kg) from <i>Stevia serrata</i> Cav. (Asteraceae) as well as the main component (5–150 mg/kg) showed hypoglycemic and antihyperglycemic effects in mice. The fractionation of the active extract led to the isolation of dammaradiene acetate (<b>1</b>), stevisalioside A (<b>2</b>), and three new chemical entities characterized by spectroscopic methods and named stevisaliosides B–D (<b>3</b>–<b>5</b>). Glycoside <b>2</b> (5 and 50 mg/kg) decreased blood glucose levels and the postprandial peak during oral glucose and insulin tolerance tests in STZ-hyperglycemic mice. Compounds <b>1</b>–<b>5</b> were tested also against PTP1B<sub>1–400</sub> and showed IC<sub>50</sub> values of 1180.9 ± 0.33, 526.8 ± 0.02, 532.1 ± 0.03, 928.2 ± 0.39, and 31.8 ± 1.09 μM, respectively. Compound <b>5</b> showed an IC<sub>50</sub> value comparable to that of ursolic acid (IC<sub>50</sub> = 30.7 ± 0.00 μM). Docking studies revealed that <b>2</b>–<b>5</b> and their aglycones bind to PTP1B<sub>1–400</sub> in a pocket formed by the C-terminal region. The volatilome of <i>S. serrata</i> was characterized by a high content of (<i>E</i>)-longipinene, spathulenol, guaiadiene, seychellene, and aromandendrene. Finally, a UHPLC-UV method was developed and validated to quantify the content of <b>2</b> in the decoction of the plant.</p>","PeriodicalId":47,"journal":{"name":"Journal of Natural Products ","volume":"87 3","pages":"501–513"},"PeriodicalIF":3.3000,"publicationDate":"2023-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Natural Products ","FirstCategoryId":"99","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.jnatprod.3c00711","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0
Abstract
A decoction of the roots (31.6–316 mg/kg) from Stevia serrata Cav. (Asteraceae) as well as the main component (5–150 mg/kg) showed hypoglycemic and antihyperglycemic effects in mice. The fractionation of the active extract led to the isolation of dammaradiene acetate (1), stevisalioside A (2), and three new chemical entities characterized by spectroscopic methods and named stevisaliosides B–D (3–5). Glycoside 2 (5 and 50 mg/kg) decreased blood glucose levels and the postprandial peak during oral glucose and insulin tolerance tests in STZ-hyperglycemic mice. Compounds 1–5 were tested also against PTP1B1–400 and showed IC50 values of 1180.9 ± 0.33, 526.8 ± 0.02, 532.1 ± 0.03, 928.2 ± 0.39, and 31.8 ± 1.09 μM, respectively. Compound 5 showed an IC50 value comparable to that of ursolic acid (IC50 = 30.7 ± 0.00 μM). Docking studies revealed that 2–5 and their aglycones bind to PTP1B1–400 in a pocket formed by the C-terminal region. The volatilome of S. serrata was characterized by a high content of (E)-longipinene, spathulenol, guaiadiene, seychellene, and aromandendrene. Finally, a UHPLC-UV method was developed and validated to quantify the content of 2 in the decoction of the plant.
期刊介绍:
The Journal of Natural Products invites and publishes papers that make substantial and scholarly contributions to the area of natural products research. Contributions may relate to the chemistry and/or biochemistry of naturally occurring compounds or the biology of living systems from which they are obtained.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.
When new compounds are reported, manuscripts describing their biological activity are much preferred.
Specifically, there may be articles that describe secondary metabolites of microorganisms, including antibiotics and mycotoxins; physiologically active compounds from terrestrial and marine plants and animals; biochemical studies, including biosynthesis and microbiological transformations; fermentation and plant tissue culture; the isolation, structure elucidation, and chemical synthesis of novel compounds from nature; and the pharmacology of compounds of natural origin.