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Rajarshi Shahu College of Pharmacy, Buldana, Department of Pharmacology
Welcome to Journal Club Presentation
Presented by : Guide Co-guide:
Mr. Nitin R. Kale Dr. S .P. Jain Mr. S.P. Borikar
1
Authors & Affilation 2
Source
Journal name : Biomedicine & Pharmacotherapy
www.elsevier.com/locate/biopha
https://doi.org/10.1016/j.biopha.2019.108638
Impact factor : 7.419
Published year : 2019
3
Introduction
 Diabetes mellitus (DM) is a chronic diseases that has become a global health
threat.
 According to the World Health Organisation (WHO) 2016 report an estimate of
422 million people globally were diagnosed with DM in 2014 while a 108 million
had diabetes in 1980.
 DM is also one of the four most common non-communicable-diseases and
currently the seventh leading cause of morbidity and mortality globally.
 high mortality rate is associated with complications such as diabetic liver disease
(DLD) which progressively develop in these patients. Liver cirrhosis,
steatohepatitis, non-alcoholic fatty liver disease (NAFLD) and hepatic carcinomas
are examples of different spectrums of DLDs that are observed in T2DM patients
with persistent hyperglycaemia
4
Cont..
 DLDs primarily develop as a consequence of hyperglycaemia, hypertriglyceridemia and insulin
resistance
 Therapeutic strategies which can efficiently prevent or reverse the adverse effects of prolonged
oxidative stress and inflammation in DM may be highly beneficial in preventing diabetic
complications such as DLDs
 A major drawback of oral antidiabetic agents is their failure to effectively cure diabetes; moreover,
they have been associated with increased side effects.
 In this regard, medicinal plants appear as promising therapeutic avenues motivated by the presence of
phytoconstituents that have numerous health benefits and may act as precursors in drug formulation
5
Drug Profile
 Catharanthus roseus or Vinca rosea / Madagascar periwinkle
 Family – Apocynaceae
 Genus – Catharatnhus
 Species – C. Roseus
 Traditionally, it was used to treat diseases like cancer, malaria, diabetes, insomnia and high blood
pressure.
 presence of indole alkaloids, flavonoids, beta sitosterol, quercetin.
 Vindoline is an indole alkaloid extracted from C. roseus which was recently been reported to possess
protein-tyrosine phosphatase 1B (PTP-1B) inhibitory effects and therefore may serve as an “insulin
sensitizer” in the management of T2DM
6
Inducer
 Single intraperitoneal injection of low dose of Streptozotocin (STZ), 40 mg/kg body
weight (b.w).
7
Aims & Objective
 Antioxidant analysis.
 Histopathological studies.
 To evaluate the effect of vindoline in hepatotoxicity induced by T2DM
conditions using glibenclamide as reference drug.
8
Materials and Methods
 Animal :
Fortyeight (48), weight : (190–230 g)
Six weeks old male Wistar Rats
Plant-derived chemical and standard drug
Vindoline was purchased from the manufacturer: Best of Chemicals
(BOC) Sciences, USA).
The standard drug : glibenclamide was purchased from a local pharmacy.
9
Experimental design
Rats were randomly divided into six groups (n = 8)
 Group N: normal control administered with vehicle only;
 Group NV: normal treated group administered with vindoline (20 mg/kg b.w);
 Group NG: normal treated group treated with glibenclamide (5 mg/ kg b.w).
 DC: diabetic control group administered with vehicle;
 Group DV: diabetic treated with 20 mg/kg b.w of vindoline;
 Group DM: diabetic treated with 5 mg/kg b.w of glibenclamide;
10
Timeline
 Duration – 56 days (8weeks)
 T2DM was induced in rats by having them drink 10% fructose solution ad
libitum for 14 days
 On day 15, STZ, 40 mg/kg.
 5 days gap.
 Daily treatment for 36 days.
 After the 8 week study period, Rats were anaesthetised and euthanized using
isoflurane gas.
11
Parameters
 Determination of the relative liver weights
Relative liver weight = (liver weight ÷ total body weight) 100g
 Liver function enzymes activity
Aspartate amino transferase (AST),
Alanine amino transferase (ALT),
Alkaline phosphatase (ALP) were measured using ABX PENTRA 400 automated
chemistry analyser machine.
12
Cont..
 Determination of lipid peroxidation
Lipid peroxidation (LPO)
 Histopathological studies
stained used haematoxylin and eosin (H & E) stain.
13
Statistical analysis
 Results were analysed using GRAPH PAD Prism software package,
Version 5.0.
 The comparisons within groups were determined by using the one way
analysis of variance (ANOVA).
14
Results 15
16
17
18
Conclusion
 experimental findings suggest that vindoline as a plant-derived
product may be of great relevance in the treatment of diabetes
mellitus and its complications owing to its anti-hyperglycemic,
antihyperlipidemic, anti-inflammatory and antioxidant activities.
19
Thank You!
SOMEONE@EXAMPLE.COM
20

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journal club presentation on effect of vindoline on hyperglycemia and liver toxicity .pptx

  • 1. Rajarshi Shahu College of Pharmacy, Buldana, Department of Pharmacology Welcome to Journal Club Presentation Presented by : Guide Co-guide: Mr. Nitin R. Kale Dr. S .P. Jain Mr. S.P. Borikar 1
  • 3. Source Journal name : Biomedicine & Pharmacotherapy www.elsevier.com/locate/biopha https://doi.org/10.1016/j.biopha.2019.108638 Impact factor : 7.419 Published year : 2019 3
  • 4. Introduction  Diabetes mellitus (DM) is a chronic diseases that has become a global health threat.  According to the World Health Organisation (WHO) 2016 report an estimate of 422 million people globally were diagnosed with DM in 2014 while a 108 million had diabetes in 1980.  DM is also one of the four most common non-communicable-diseases and currently the seventh leading cause of morbidity and mortality globally.  high mortality rate is associated with complications such as diabetic liver disease (DLD) which progressively develop in these patients. Liver cirrhosis, steatohepatitis, non-alcoholic fatty liver disease (NAFLD) and hepatic carcinomas are examples of different spectrums of DLDs that are observed in T2DM patients with persistent hyperglycaemia 4
  • 5. Cont..  DLDs primarily develop as a consequence of hyperglycaemia, hypertriglyceridemia and insulin resistance  Therapeutic strategies which can efficiently prevent or reverse the adverse effects of prolonged oxidative stress and inflammation in DM may be highly beneficial in preventing diabetic complications such as DLDs  A major drawback of oral antidiabetic agents is their failure to effectively cure diabetes; moreover, they have been associated with increased side effects.  In this regard, medicinal plants appear as promising therapeutic avenues motivated by the presence of phytoconstituents that have numerous health benefits and may act as precursors in drug formulation 5
  • 6. Drug Profile  Catharanthus roseus or Vinca rosea / Madagascar periwinkle  Family – Apocynaceae  Genus – Catharatnhus  Species – C. Roseus  Traditionally, it was used to treat diseases like cancer, malaria, diabetes, insomnia and high blood pressure.  presence of indole alkaloids, flavonoids, beta sitosterol, quercetin.  Vindoline is an indole alkaloid extracted from C. roseus which was recently been reported to possess protein-tyrosine phosphatase 1B (PTP-1B) inhibitory effects and therefore may serve as an “insulin sensitizer” in the management of T2DM 6
  • 7. Inducer  Single intraperitoneal injection of low dose of Streptozotocin (STZ), 40 mg/kg body weight (b.w). 7
  • 8. Aims & Objective  Antioxidant analysis.  Histopathological studies.  To evaluate the effect of vindoline in hepatotoxicity induced by T2DM conditions using glibenclamide as reference drug. 8
  • 9. Materials and Methods  Animal : Fortyeight (48), weight : (190–230 g) Six weeks old male Wistar Rats Plant-derived chemical and standard drug Vindoline was purchased from the manufacturer: Best of Chemicals (BOC) Sciences, USA). The standard drug : glibenclamide was purchased from a local pharmacy. 9
  • 10. Experimental design Rats were randomly divided into six groups (n = 8)  Group N: normal control administered with vehicle only;  Group NV: normal treated group administered with vindoline (20 mg/kg b.w);  Group NG: normal treated group treated with glibenclamide (5 mg/ kg b.w).  DC: diabetic control group administered with vehicle;  Group DV: diabetic treated with 20 mg/kg b.w of vindoline;  Group DM: diabetic treated with 5 mg/kg b.w of glibenclamide; 10
  • 11. Timeline  Duration – 56 days (8weeks)  T2DM was induced in rats by having them drink 10% fructose solution ad libitum for 14 days  On day 15, STZ, 40 mg/kg.  5 days gap.  Daily treatment for 36 days.  After the 8 week study period, Rats were anaesthetised and euthanized using isoflurane gas. 11
  • 12. Parameters  Determination of the relative liver weights Relative liver weight = (liver weight ÷ total body weight) 100g  Liver function enzymes activity Aspartate amino transferase (AST), Alanine amino transferase (ALT), Alkaline phosphatase (ALP) were measured using ABX PENTRA 400 automated chemistry analyser machine. 12
  • 13. Cont..  Determination of lipid peroxidation Lipid peroxidation (LPO)  Histopathological studies stained used haematoxylin and eosin (H & E) stain. 13
  • 14. Statistical analysis  Results were analysed using GRAPH PAD Prism software package, Version 5.0.  The comparisons within groups were determined by using the one way analysis of variance (ANOVA). 14
  • 16. 16
  • 17. 17
  • 18. 18
  • 19. Conclusion  experimental findings suggest that vindoline as a plant-derived product may be of great relevance in the treatment of diabetes mellitus and its complications owing to its anti-hyperglycemic, antihyperlipidemic, anti-inflammatory and antioxidant activities. 19