TY - JOUR
T1 - Mechanistic understanding of PtyroneTM
T2 - A plant based natural anti diabetic product
AU - Dound, Yogesh Arun
AU - Chaudhary, Sameer
AU - Chaudhary, Sapana Sameer
AU - Rawat, Sakshi
AU - Alqarni, Mohammed H.
AU - Ahmad, Malik M.
AU - Geesi, Mohammed H.
AU - Alam, Pravej
N1 - Publisher Copyright:
© 2021 The Author(s)
PY - 2021/7
Y1 - 2021/7
N2 - Objective: To investigate the combinatorial effect of hydroalcoholic extracts of Andrographis paniculata Nees. and Pterocarpus marsupium Roxb. plants prospective to diabetes management. Methods: Taking a lead from the scientific literature, in silico studies have also been designed for the screening of anti-diabetic targets against andrographolide and pterostilbene compounds followed by in vivo studies from Andrographis paniculata Nees. and Pterocarpus marsupium Roxb. Furthermore, the diabetes was induced by STZ model and the impact of Andrographis paniculata Nees. and Pterocarpus marsupium Roxb. have been conformed by relative expression studies by qPCR. Results: Our results have shown that andrographolide and pterostilbene are SGLT2 inhibitors and selective PPARγ agonists in in silico studies. Later, during in vivo mRNA expression studies confirming the same pattern. The findings of the study has shown to overcome the common knowledge of the only C–glycoside based molecules inhibiting the SGLT2. Conclusions: The possible mechanism for PtyroneTM in the management of diabetes could be a selective PPARγ agonist, GLUT4 translocation and SGLT2 inhibition molecule.
AB - Objective: To investigate the combinatorial effect of hydroalcoholic extracts of Andrographis paniculata Nees. and Pterocarpus marsupium Roxb. plants prospective to diabetes management. Methods: Taking a lead from the scientific literature, in silico studies have also been designed for the screening of anti-diabetic targets against andrographolide and pterostilbene compounds followed by in vivo studies from Andrographis paniculata Nees. and Pterocarpus marsupium Roxb. Furthermore, the diabetes was induced by STZ model and the impact of Andrographis paniculata Nees. and Pterocarpus marsupium Roxb. have been conformed by relative expression studies by qPCR. Results: Our results have shown that andrographolide and pterostilbene are SGLT2 inhibitors and selective PPARγ agonists in in silico studies. Later, during in vivo mRNA expression studies confirming the same pattern. The findings of the study has shown to overcome the common knowledge of the only C–glycoside based molecules inhibiting the SGLT2. Conclusions: The possible mechanism for PtyroneTM in the management of diabetes could be a selective PPARγ agonist, GLUT4 translocation and SGLT2 inhibition molecule.
KW - Andrographis paniculata Nees.
KW - Andrographolide
KW - Diabetes mellitus type 2
KW - Pterocarpus marsupium Roxb.
KW - Pterostilbene
KW - Ptyrone
UR - http://www.scopus.com/inward/record.url?scp=85105521243&partnerID=8YFLogxK
U2 - 10.1016/j.jksus.2021.101454
DO - 10.1016/j.jksus.2021.101454
M3 - Article
AN - SCOPUS:85105521243
SN - 1018-3647
VL - 33
JO - Journal of King Saud University - Science
JF - Journal of King Saud University - Science
IS - 5
M1 - 101454
ER -