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Antidiabetic Sterols from Peniocereus greggii Roots.

Authors :
Muñoz-Gómez RJ
Rivero-Cruz I
Ovalle-Magallanes B
Linares E
Bye R
Tovar AR
Noriega LG
Tovar-Palacio C
Mata R
Source :
ACS omega [ACS Omega] 2022 Apr 08; Vol. 7 (15), pp. 13144-13154. Date of Electronic Publication: 2022 Apr 08 (Print Publication: 2022).
Publication Year :
2022

Abstract

The roots of the cactus Peniocereus greggii , which grows in Northern Mexico and in the south of Arizona, are highly valued by the Pima to treat diabetes and other illnesses, such as breast pain and common cold. As part of our chemical and pharmacological investigation on medicinal plants used for treating diabetes, herein we report the hypoglycemic and antihyperglycemic action of a decoction prepared from the roots of the plant. The active compounds were a series of cholestane steroids, namely, peniocerol ( 2 ), desoxyviperidone ( 3 ), viperidone ( 4 ), and viperidinone ( 5 ). Also, a new chemical entity was obtained from an alkalinized chloroform extract (CE1), which was characterized as 3,6-dihydroxycholesta-5,8(9),14-trien-7-one ( 6 ) by spectroscopic means. Desoxyviperidone ( 3 ) showed an antihyperglycemic action during an oral glucose tolerance test. Compound 3 was also able to decrease blood glucose levels during an intraperitoneal insulin tolerance test in hyperglycemic mice only in combination with insulin, thus behaving as an insulin sensitizer agent. Nevertheless, mitochondrial bioenergetic experiments revealed that compounds 3 and 6 increased basal respiration and proton leak, without affecting the respiration associated with ATP production in C2C12 myotubes. Finally, an ultraefficiency liquid chromatographic method for quantifying desoxyviperidone ( 3 ) and viperidone ( 4 ) in the crude drug was developed and validated. Altogether, our results demonstrate that Peniocereus greggii decoction possesses a hypoglycemic and antihyperglycemic action in vivo, that sterols 2 and 6 promotes insulin secretion in vitro, and that desoxyviperidone ( 3 ) physiologically behaves as an insulin sensitizer agent by a mechanism that may involve mitochondrial proton leak.<br />Competing Interests: The authors declare no competing financial interest.<br /> (© 2022 The Authors. Published by American Chemical Society.)

Details

Language :
English
ISSN :
2470-1343
Volume :
7
Issue :
15
Database :
MEDLINE
Journal :
ACS omega
Publication Type :
Academic Journal
Accession number :
35474764
Full Text :
https://doi.org/10.1021/acsomega.2c00595