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9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation. / Khvostov, Mikhail V; Gladkova, Elizaveta D; Borisov, Sergey A и др.

в: Pharmaceutics, Том 15, № 1, 44, 01.01.2023.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Khvostov, MV, Gladkova, ED, Borisov, SA, Fedotova, MS, Zhukova, NA, Marenina, MK, Meshkova, YV, Valutsa, N, Luzina, OA, Tolstikova, TG & Salakhutdinov, NF 2023, '9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation', Pharmaceutics, Том. 15, № 1, 44. https://doi.org/10.3390/pharmaceutics15010044

APA

Khvostov, M. V., Gladkova, E. D., Borisov, S. A., Fedotova, M. S., Zhukova, N. A., Marenina, M. K., Meshkova, Y. V., Valutsa, N., Luzina, O. A., Tolstikova, T. G., & Salakhutdinov, N. F. (2023). 9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation. Pharmaceutics, 15(1), [44]. https://doi.org/10.3390/pharmaceutics15010044

Vancouver

Khvostov MV, Gladkova ED, Borisov SA, Fedotova MS, Zhukova NA, Marenina MK и др. 9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation. Pharmaceutics. 2023 янв. 1;15(1):44. doi: 10.3390/pharmaceutics15010044

Author

Khvostov, Mikhail V ; Gladkova, Elizaveta D ; Borisov, Sergey A и др. / 9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation. в: Pharmaceutics. 2023 ; Том 15, № 1.

BibTeX

@article{0cfc3ecf0b284eac8db61e0e1d2d9a21,
title = "9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation",
abstract = "Several novel 9-N-n-alkyl derivatives of berberine (C5, C7, C10, C12) were synthesized. They were analyzed in vitro and in vivo for their hypoglycemic activity. In vitro studies showed that the derivatives with shorter alkyl substitutes at concentrations ranging from 2.5 to 10 μM were able to stimulate glucose consumption by HepG2 cells more prominently than the derivatives with longer substitutes (C10 and C12). All compounds demonstrated a better effect compared to berberine. Their impact on cells' viability also depended on the alkyl substitutes length, but in this case, C10 and C12 derivatives demonstrated the best results. A similar correlation was also found in the OGTT, where the C5 derivative demonstrated a pronounced hypoglycemic effect at a dose of 15 mg/kg and C12 was less effective. This compound was further investigated in C57BL/6Ay mice for four weeks and was administered at a dose of 15 mg/kg. Pronounced effect of C12 on carbohydrate metabolism in mice was discovered: there was a decrease in fasting glucose levels and an increase in glucose tolerance in OGTT on the 14th and 28th days of the experiment. However, at the end of the experiment, signs of hepatosis exacerbation and an increase in the content of hepatic aminotransferases in blood were found.",
author = "Khvostov, {Mikhail V} and Gladkova, {Elizaveta D} and Borisov, {Sergey A} and Fedotova, {Marina S} and Zhukova, {Nataliya A} and Marenina, {Mariya K} and Meshkova, {Yulia V} and Nicolae Valutsa and Luzina, {Olga A} and Tolstikova, {Tatiana G} and Salakhutdinov, {Nariman F}",
note = "Funding: This research was financially supported by the Russian Science Foundation, project No. 20-13-00029.",
year = "2023",
month = jan,
day = "1",
doi = "10.3390/pharmaceutics15010044",
language = "English",
volume = "15",
journal = "Pharmaceutics",
issn = "1999-4923",
publisher = "Multidisciplinary Digital Publishing Institute (MDPI)",
number = "1",

}

RIS

TY - JOUR

T1 - 9-N-n-alkyl Berberine Derivatives: Hypoglycemic Activity Evaluation

AU - Khvostov, Mikhail V

AU - Gladkova, Elizaveta D

AU - Borisov, Sergey A

AU - Fedotova, Marina S

AU - Zhukova, Nataliya A

AU - Marenina, Mariya K

AU - Meshkova, Yulia V

AU - Valutsa, Nicolae

AU - Luzina, Olga A

AU - Tolstikova, Tatiana G

AU - Salakhutdinov, Nariman F

N1 - Funding: This research was financially supported by the Russian Science Foundation, project No. 20-13-00029.

PY - 2023/1/1

Y1 - 2023/1/1

N2 - Several novel 9-N-n-alkyl derivatives of berberine (C5, C7, C10, C12) were synthesized. They were analyzed in vitro and in vivo for their hypoglycemic activity. In vitro studies showed that the derivatives with shorter alkyl substitutes at concentrations ranging from 2.5 to 10 μM were able to stimulate glucose consumption by HepG2 cells more prominently than the derivatives with longer substitutes (C10 and C12). All compounds demonstrated a better effect compared to berberine. Their impact on cells' viability also depended on the alkyl substitutes length, but in this case, C10 and C12 derivatives demonstrated the best results. A similar correlation was also found in the OGTT, where the C5 derivative demonstrated a pronounced hypoglycemic effect at a dose of 15 mg/kg and C12 was less effective. This compound was further investigated in C57BL/6Ay mice for four weeks and was administered at a dose of 15 mg/kg. Pronounced effect of C12 on carbohydrate metabolism in mice was discovered: there was a decrease in fasting glucose levels and an increase in glucose tolerance in OGTT on the 14th and 28th days of the experiment. However, at the end of the experiment, signs of hepatosis exacerbation and an increase in the content of hepatic aminotransferases in blood were found.

AB - Several novel 9-N-n-alkyl derivatives of berberine (C5, C7, C10, C12) were synthesized. They were analyzed in vitro and in vivo for their hypoglycemic activity. In vitro studies showed that the derivatives with shorter alkyl substitutes at concentrations ranging from 2.5 to 10 μM were able to stimulate glucose consumption by HepG2 cells more prominently than the derivatives with longer substitutes (C10 and C12). All compounds demonstrated a better effect compared to berberine. Their impact on cells' viability also depended on the alkyl substitutes length, but in this case, C10 and C12 derivatives demonstrated the best results. A similar correlation was also found in the OGTT, where the C5 derivative demonstrated a pronounced hypoglycemic effect at a dose of 15 mg/kg and C12 was less effective. This compound was further investigated in C57BL/6Ay mice for four weeks and was administered at a dose of 15 mg/kg. Pronounced effect of C12 on carbohydrate metabolism in mice was discovered: there was a decrease in fasting glucose levels and an increase in glucose tolerance in OGTT on the 14th and 28th days of the experiment. However, at the end of the experiment, signs of hepatosis exacerbation and an increase in the content of hepatic aminotransferases in blood were found.

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85146618299&origin=inward&txGid=9ed5afa5a77d15af8dfb8e73f02f8660

U2 - 10.3390/pharmaceutics15010044

DO - 10.3390/pharmaceutics15010044

M3 - Article

C2 - 36678673

VL - 15

JO - Pharmaceutics

JF - Pharmaceutics

SN - 1999-4923

IS - 1

M1 - 44

ER -

ID: 43624586