TY - JOUR
T1 - Biochemical and tissue physiopathological evaluation of the preclinical efficacy of Solanum torvum Swartz leaves for treating oxidative impairment in rats administered a β-cell-toxicant (STZ)
AU - Sani, Saidu
AU - Lawal, Bashir
AU - Ejeje, Jerius N.
AU - Aliu, Tawakalitu B.
AU - Onikanni, Amos S.
AU - Uchewa, Onwe O.
AU - Ovoh, Joy C.
AU - Ekpa, Faith U.
AU - Ozoagu, Chikezie D.
AU - Akuma, Tochukwu S.
AU - Onyeji, Success C.
AU - Obialor, Amara
AU - Alotaibi, Saqer S.
AU - Albogami, Sarah M.
AU - De Waard, Michel
AU - Batiha, Gaber El Saber
AU - Huang, Tse Hung
AU - Wu, Alexander T.H.
N1 - Funding Information:
Acknowledgment: M.D.W. thanks the French Agence Nationale de la Recherche and the Région Pays de la Loire for financial support (CoV2-E-TAR[1]GET-grant number: 2020 07132 ). Author would also like to acknowledge the Taif University Researchers Supporting Project [number TURSP-2020/202 ], Taif University, Taif, Saudi Arabia.
Funding Information:
Alexander TH Wu is funded by the Ministry of Science and Technology with grant numbers: 111-2314-B-038 -098 and 111-2314-B-038 -142 . Tse Hung Huang was supported by grant nos. CMRPG2H0362 and CORPG2J0042 .
Funding Information:
Alexander TH Wu is funded by the Ministry of Science and Technology with grant numbers: 111-2314-B-038 -098 and 111-2314-B-038 -142. Tse Hung Huang was supported by grant nos. CMRPG2H0362 and CORPG2J0042.Acknowledgment: M.D.W. thanks the French Agence Nationale de la Recherche and the Région Pays de la Loire for financial support (CoV2-E-TAR[1]GET-grant number: 2020 07132). Author would also like to acknowledge the Taif University Researchers Supporting Project [number TURSP-2020/202], Taif University, Taif, Saudi Arabia.
Publisher Copyright:
© 2022 The Authors
PY - 2022/10
Y1 - 2022/10
N2 - The current study evaluated the protective role of Solanum torvum Swartz against diabetes-induced oxidative stress and tissue impairment in streptozotocin (STZ)-intoxicated rats. Rats with STZ (40 mg/kg intraperitoneally (i.p.))-induced diabetes were divided into five groups (n = 5) and treated with (i) normal saline, (ii) 150 mg/kg body weight (BW) of the ethanol extract of S. torvum leaf (EESTL), (ii) 300 mg/kg BW EESTL, (iv) 100 mg/kg BW metformin, and (v) 50 m/kg BW metformin + 100 mg/kg BW EESTL orally for 21 days. Our results revealed that the EESTL displayed dose-dependent ferric-reducing antioxidant power (FRAP) activity, scavenged DPPH radicals (IC50) = 13.52 ± 0.45 µg/mL), and inhibited lipid peroxidation in an in vitro models. In addition, the EESTL demonstrated dose-dependent inhibitory activity against α-amylase (IC50 =138.46 ± 3.97 µg/mL) and promoted glucose uptake across plasma membranes of yeast cells in a manner comparable to that of metformin. Interestingly, the extract demonstrated in vivo blood glucose normalization effects with concomitant increased activities of antioxidant parameters (superoxide dismutase (SOD), catalase, and reduced glutathione (GSH)) while decreasing malondialdehyde (MDA) levels when compared to untreated rats. Similarly, serum biochemical alterations, and tissues (liver, kidney, and pancreases) histopathological aberrations in untreated rats with STZ-induced diabetes were attenuated by treatment with the EESTL. Biometabolite characterization of the extract identified gallic acid (45.81 ppm), catechin (1.18 ppm), p-coumaric acid (1.43e−1 ppm), DL-proline 5-oxo-methyl ester (9.16 %, retention time (RT): 8.57 min), salicylic acid (3.26% and 7.61 min), and butylated hydroxytoluene (4.75%, RT: 10.18 min) as the major polyphenolic compounds in the plant extract. In conclusion, our study provides preclinical evidence of the antioxidant properties and oxidative stress-preventing role of S. torvum in STZ-dosed diabetic rats. Taken together, the EESTL represents a reserve of bioactive metabolites for managing diabetes and associated complications.
AB - The current study evaluated the protective role of Solanum torvum Swartz against diabetes-induced oxidative stress and tissue impairment in streptozotocin (STZ)-intoxicated rats. Rats with STZ (40 mg/kg intraperitoneally (i.p.))-induced diabetes were divided into five groups (n = 5) and treated with (i) normal saline, (ii) 150 mg/kg body weight (BW) of the ethanol extract of S. torvum leaf (EESTL), (ii) 300 mg/kg BW EESTL, (iv) 100 mg/kg BW metformin, and (v) 50 m/kg BW metformin + 100 mg/kg BW EESTL orally for 21 days. Our results revealed that the EESTL displayed dose-dependent ferric-reducing antioxidant power (FRAP) activity, scavenged DPPH radicals (IC50) = 13.52 ± 0.45 µg/mL), and inhibited lipid peroxidation in an in vitro models. In addition, the EESTL demonstrated dose-dependent inhibitory activity against α-amylase (IC50 =138.46 ± 3.97 µg/mL) and promoted glucose uptake across plasma membranes of yeast cells in a manner comparable to that of metformin. Interestingly, the extract demonstrated in vivo blood glucose normalization effects with concomitant increased activities of antioxidant parameters (superoxide dismutase (SOD), catalase, and reduced glutathione (GSH)) while decreasing malondialdehyde (MDA) levels when compared to untreated rats. Similarly, serum biochemical alterations, and tissues (liver, kidney, and pancreases) histopathological aberrations in untreated rats with STZ-induced diabetes were attenuated by treatment with the EESTL. Biometabolite characterization of the extract identified gallic acid (45.81 ppm), catechin (1.18 ppm), p-coumaric acid (1.43e−1 ppm), DL-proline 5-oxo-methyl ester (9.16 %, retention time (RT): 8.57 min), salicylic acid (3.26% and 7.61 min), and butylated hydroxytoluene (4.75%, RT: 10.18 min) as the major polyphenolic compounds in the plant extract. In conclusion, our study provides preclinical evidence of the antioxidant properties and oxidative stress-preventing role of S. torvum in STZ-dosed diabetic rats. Taken together, the EESTL represents a reserve of bioactive metabolites for managing diabetes and associated complications.
KW - Antioxidant
KW - Diabetes mellitus
KW - Organ histopathology
KW - Oxidative stress
KW - Solanum torvum Swartz
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U2 - 10.1016/j.biopha.2022.113605
DO - 10.1016/j.biopha.2022.113605
M3 - Article
C2 - 36030588
AN - SCOPUS:85136563654
SN - 0753-3322
VL - 154
JO - Biomedicine and Pharmacotherapy
JF - Biomedicine and Pharmacotherapy
M1 - 113605
ER -