Iwara A. Iwara , Oju R. Ibor , Eve Mboso , Eyong Ubana Eyong , Augustine Arukwe
{"title":"Molecular and biochemical responses in Wistar rats treated with extracts from a hyperglycemia and diabetes-associated therapeutic Hensia crinita","authors":"Iwara A. Iwara , Oju R. Ibor , Eve Mboso , Eyong Ubana Eyong , Augustine Arukwe","doi":"10.1016/j.phyplu.2025.100849","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Diabetes, marked by insulin resistance, disrupts metabolic processes and causes significant complications. Herbal remedies are increasingly recognized for their potential in diabetes management, particularly in developing countries.</div></div><div><h3>Purpose</h3><div>To study the effects of <em>Hensia crinita</em> (<em>H. crinita</em>) extract on hyperglycemia and related therapeutic responses in Wistar rats.</div></div><div><h3>Methods</h3><div>Type 2 diabetes was induced with 10% fructose diet and 40 mg/kg streptozotocin (STZ). Thereafter, diabetic rats were treated with <em>H. crinita</em> leaf extracts at 200 and 400 mg/kg body weight, twice daily for 21 days. We used metformin (MET: 500 mg/kg body weight) treated rats as a positive control group.</div></div><div><h3>Results</h3><div>Our results showed that <em>H. crinita</em> extract significantly lowered fasting blood glucose (FBG) levels and increased body weight in diabetic rats. Molecular analysis revealed reductions in mRNA expression for insulin-responsive glucose transporter (<em>ir-glut</em>), <em>leptin</em>, proprotein convertase subtilisin/kexin type 9 (<em>pcsk9</em>), cardiac troponin (<em>crt</em>), estrogen receptor 1 (<em>esr-1</em>), fatty acid synthase (<em>fasn</em>) and melatonin (mt) in treated rats, compared to controls. Furthermore, hepatic biochemical analysis showed that AST, ALT, ALP and γ-GGT increased in diabetic control animal and <em>H. crinita</em> produced decreases that paralleled melatonin effects. Additionally, <em>H. crinita</em> treatment increased plasma estradiol (E2) and testosterone (T) levels and significantly reduced inflammatory markers, and these responses were comparable to MET effects.</div></div><div><h3>Conclusion</h3><div>These findings suggest that <em>H. crinita</em> exerts anti-hyperglycemic effects by modulating inflammation, hormonal balance, and key glucose metabolic enzymes, representing a potential therapeutic agent for diabetes treatment.</div></div>","PeriodicalId":34599,"journal":{"name":"Phytomedicine Plus","volume":"5 3","pages":"Article 100849"},"PeriodicalIF":0.0000,"publicationDate":"2025-07-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Phytomedicine Plus","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667031325001204","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Diabetes, marked by insulin resistance, disrupts metabolic processes and causes significant complications. Herbal remedies are increasingly recognized for their potential in diabetes management, particularly in developing countries.
Purpose
To study the effects of Hensia crinita (H. crinita) extract on hyperglycemia and related therapeutic responses in Wistar rats.
Methods
Type 2 diabetes was induced with 10% fructose diet and 40 mg/kg streptozotocin (STZ). Thereafter, diabetic rats were treated with H. crinita leaf extracts at 200 and 400 mg/kg body weight, twice daily for 21 days. We used metformin (MET: 500 mg/kg body weight) treated rats as a positive control group.
Results
Our results showed that H. crinita extract significantly lowered fasting blood glucose (FBG) levels and increased body weight in diabetic rats. Molecular analysis revealed reductions in mRNA expression for insulin-responsive glucose transporter (ir-glut), leptin, proprotein convertase subtilisin/kexin type 9 (pcsk9), cardiac troponin (crt), estrogen receptor 1 (esr-1), fatty acid synthase (fasn) and melatonin (mt) in treated rats, compared to controls. Furthermore, hepatic biochemical analysis showed that AST, ALT, ALP and γ-GGT increased in diabetic control animal and H. crinita produced decreases that paralleled melatonin effects. Additionally, H. crinita treatment increased plasma estradiol (E2) and testosterone (T) levels and significantly reduced inflammatory markers, and these responses were comparable to MET effects.
Conclusion
These findings suggest that H. crinita exerts anti-hyperglycemic effects by modulating inflammation, hormonal balance, and key glucose metabolic enzymes, representing a potential therapeutic agent for diabetes treatment.