Paper Title
TYPE 2 DIABETES: EVALUATING THE EFFECTS OF CLARAMINE ON INSULIN- MEDIATED GLUCOSE REGULATION IN HEPATOMA (HEPG2) CELL LINE.
Article Identifiers
Authors
DR. LAMIDI, TAJUDEEN BABATUNDE , KILEDU, ISREAL AHMADU
Keywords
Keywords: Diabetes, Insulin, PTPs, Claramine, Hepatoma cell line, Metabolic disease
Abstract
ABSTRACT Diabetes is a chronic, metabolic disease characterized by elevated levels of blood glucose (or blood sugar), which leads over time to serious damage to the heart, blood vessels, eyes, kidneys and nerves. The most common is type 2 diabetes, usually in adults, which occurs when the body becomes resistant to insulin or doesn't make enough insulin. Protein tyrosine phosphatises (PTPs) are critical antagonist of insulin receptor (IR) signalling. Their inhibition with pharmacological inhibitory agents can play the role of insulin thus facilitating the uptake of glucose and the inhibition of lipolysis. Elevated PTPIB activity underlies insulin resistance in type 2 diabetes. Several experiments have shown that PTPIB is implicated in glucose regulation obesity and type-2 diabetes. Claramine is a novel synthetic chemical agent which possess selective inhibitory activity against PTPIB. This research was aimed at unveiling the effects of claramine on insulin-mediated glucose regulation in Hepatoma (HepG2) cell lines. Research materials including Hep G2 cell line, T-75 flasks, Eppendorf tubes, 96-well plates, Bradford reagent test kit, cell culture media (Dulbecco's Modified Eagle Medium) (DMEM) and all reagents for buffer preparation was purchased. First experiment was conducted to test the viability of the HepG 2 cell lines using standard procedure. Second round of experiment was conducted to culture the HepG 2 cells at 37OC. The cells were divided into 6 wells plates and allowed to adhere for 24 hours. After adherence, the cells were treated with high glucose and different concentrations of insulin and claramine. The determination of glucose utilisation by the cells was done with multiscan-FC spectrophotometer at 540nm and the amount of glucose utilised by the cell was calculated and use for protein normalisation. Combination of 50nm of insulin with various concentrations of claramine showed trend in the uptake of glucose by Hep2 cells with highest uptake at 2.0um of claramine. However, with 100nm insulin there was relative little and irregular variation in glucose uptake by HepG 2 cells with different concentrations of claramine. Also, glucose utilisation with respect to joint variation of insulin and claramine concentrations showed increase uptake at 50nm insulin and 1um claramine. Hepatoma cell lines can be used to investigate the glucose uptake and glucose metabolism in hepatocyte. claramine is a first class highly selective inhibitor of protein tyrosine phosphtase IB (PTPIB). It is therefore eminent that inhibitors of PTPIB plays important role as efficient therapeutic target for type-II diabetes and obesity by increasing insulin and leptin sensitivity.
Downloads
How To Cite
"TYPE 2 DIABETES: EVALUATING THE EFFECTS OF CLARAMINE ON INSULIN- MEDIATED GLUCOSE REGULATION IN HEPATOMA (HEPG2) CELL LINE.", IJNRD - INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT (www.IJNRD.org), ISSN:2456-4184, Vol.8, Issue 11, page no.a710-a719, November-2023, Available :https://ijnrd.org/papers/IJNRD2311078.pdf
Issue
Volume 8 Issue 11, November-2023
Pages : a710-a719
Other Publication Details
Paper Reg. ID: IJNRD_205279
Published Paper Id: IJNRD2311078
Downloads: 000121155
Research Area: Pharmacy
Country: BALI, TARABA , Nigeria
Published Paper PDF: https://ijnrd.org/papers/IJNRD2311078.pdf
Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2311078
About Publisher
Journal Name: INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT(IJNRD)
ISSN: 2456-4184 | IMPACT FACTOR: 8.76 Calculated By Google Scholar | ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.76 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator
Publisher: IJNRD (IJ Publication) Janvi Wave
Licence
This work is licensed under a Creative Commons Attribution 4.0 International License and The Open Definition


Publication Timeline
Article Preview: View Full Paper
Call For Paper
IJNRD is Scholarly open access journals, Peer-reviewed, and Refereed Journals, High Impact factor 8.76 (Calculate by google scholar and Semantic Scholar | AI-Powered Research Tool), Multidisciplinary, Monthly, Indexing in all major database & Metadata, Citation Generator, Digital Object Identifier(DOI) with Open-Access Publications.
INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT (IJNRD) aims to explore advances in research pertaining to applied, theoretical and experimental Technological studies. The goal is to promote scientific information interchange between researchers, developers, engineers, students, and practitioners working in and around the world. IJNRD will provide an opportunity for practitioners and educators of engineering field to exchange research evidence, models of best practice and innovative ideas.
Indexing In Google Scholar, SSRN, ResearcherID-Publons, Semantic Scholar | AI-Powered Research Tool, Microsoft Academic, Academia.edu, arXiv.org, Research Gate, CiteSeerX, ResearcherID Thomson Reuters, Mendeley : reference manager, DocStoc, ISSUU, Scribd, and many more
How to submit the paper?
By Our website
Click Here to Submit Paper Online
Important Dates for Current issue
Paper Submission Open For: August 2025
Current Issue: Volume 10 | Issue 8
Last Date for Paper Submission: Till 31-Aug-2025
Notification of Review Result: Within 1-2 Days after Submitting paper.
Publication of Paper: Within 01-02 Days after Submititng documents.
Frequency: Monthly (12 issue Annually).
Journal Type: International Peer-reviewed, Refereed, and Open Access Journal.
Subject Category: Research Area