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Related Concept Videos

Insulin: Biosynthesis, Chemistry, and Preparation01:25

Insulin: Biosynthesis, Chemistry, and Preparation

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The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
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Sustained Administration of &#946;-cell Mitogens to Intact Mouse Islets Ex Vivo Using Biodegradable Poly(lactic-co-glycolic acid) Microspheres
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Bile acid-polymer-probucol microparticles: protective effect on pancreatic β-cells and decrease in type 1 diabetes

Armin Mooranian1, Nassim Zamani1, Giuseppe Luna1

  • 1Biotechnology and Drug Development Research Laboratory, School of Pharmacy and Biomedical Sciences, Curtin Health Innovation Research Institute, Curtin University , Perth , Australia.

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|September 27, 2019
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Summary
This summary is machine-generated.

The combination of probucol (PB) and ursodeoxycholic acid (UDCA) enhanced PB absorption and reduced inflammation, suggesting potential for type 1 diabetes prevention.

Keywords:
Type-1 diabetesbile acidsnanoencapsulation technologyprobucolursodeoxycholic acid

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Area of Science:

  • Pharmacology
  • Immunology
  • Endocrinology

Background:

  • Probucol (PB) exhibits anti-inflammatory and beta-cell protective effects, showing potential for diabetes treatment.
  • Ursodeoxycholic acid (UDCA), an anti-inflammatory bile acid, was incorporated to optimize PB's anti-inflammatory properties.

Purpose of the Study:

  • To evaluate the absorption, tissue distribution, anti-inflammatory effects, and type 1 diabetes prevention of PB when combined with UDCA.
  • To compare PB-UDCA microcapsules with PB powder and PB microcapsules in a mouse model.

Main Methods:

  • Balb/c mice were administered PB powder, PB microcapsules, or PB-UDCA microcapsules daily for one week.
  • Type 1 diabetes was induced using alloxan, and treatment was continued for three days post-confirmation.
  • PB concentrations, cytokine levels (Interferon gamma), blood glucose, and survival rates were analyzed.

Main Results:

  • The PB-UDCA group exhibited the highest PB concentrations in blood and various tissues, including the gut, liver, spleen, brain, and white adipose tissue.
  • PB-UDCA significantly reduced plasma Interferon gamma levels, indicating potent anti-inflammatory effects.
  • While blood glucose levels were similar across groups, the PB-UDCA group showed the highest survival rate.

Conclusions:

  • PB-UDCA demonstrated superior PB absorption and tissue distribution compared to PB alone.
  • The combination therapy effectively reduced inflammation and improved survival in a type 1 diabetes mouse model.
  • PB-UDCA holds promise for enhanced therapeutic outcomes in diabetes management.