Rat Pancreatic Islets

Cat.No.: CSC-C9295J

Species: Rat

Source: Pancreatic Islet; Pancreas

  • Specification
  • Background
  • Scientific Data
  • Q & A
  • Customer Review
Cat.No.
CSC-C9295J
Description
Rat Pancreatic Islets from Creative Bioarray are isolated from the pancreas of Sprague–Dawley rat using Collagenase P and purified using Ficoll density gradient.
Species
Rat
Source
Pancreatic Islet; Pancreas
Disease
Diabetes
Storage
Liquid Nitrogen (-180 °C).
Quality Control
Rat Pancreatic Islets are tested for their viability using FDA/PI, purity using Dithizone staining, static insulin secretion in response to 14 mM glucose. Upon request, dynamic insulin secretion and calcium imaging in response to glucose and other stimulators can be performed.
Storage and Shipping
Creative Bioarray ships frozen cells on dry ice. On receipt, immediately transfer frozen cells to liquid nitrogen (-180 °C) until ready for experimental use. Never can cells be kept at -20 °C.
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.

Rat Pancreatic Islets are native primary multicellular units isolated from laboratory rat pancreas. Rat pancreatic islets have been established as a physiologically relevant in vitro model to study normal pancreatic endocrine function. Rat pancreatic islets contain multiple hormone-producing endocrine cell types including insulin-producing β cells, glucagon-producing α cells, somatostatin-producing δ cells, and pancreatic polypeptide-producing PP cells. Rat Pancreatic Islets allow for advanced studies of normal cell-cell interactions and hormone secretion since they most closely mimic native pancreas.

Rat Pancreatic Islets are glucose responsive for insulin secretion in culture and maintain many metabolic and signaling pathways used by β-cells for nutrient sensing and hormone secretion. They can be used to study insulin synthesis, secretion, and storage, β-cell viability, proliferation and survival, normal physiology, and β-cell dysfunction. Rat pancreatic islets are frequently used to model type 1 diabetes (T1D), type 2 diabetes (T2D), islet inflammation, glucotoxicity or lipotoxicity-mediated β-cell dysfunction. Additionally, these Islets can be used for pharmaceutical and translational studies including antidiabetic therapies, insulin secretagogues, and cytoprotective studies. Rat pancreatic islets can also be used to study transplantation including islet viability and recovery of function after transplantation.

Dietary Supplementation with Yerba Mate Infusion Increases IRS-1 and PI3K mRNA Levels and Enhances Insulin Sensitivity and Secretion in Rat Pancreatic Islets

Yerba mate (YM), possesses antioxidant, diuretic, cardio-protective and hypoglycaemic effects. However, the mechanisms involved in YM pancreatic islets have not been determined. Maiztegui et al. analyzed YM effects on insulin sensitivity and glucose stimulated insulin secretion (GSIS), hoping to identify key pathways involved in YM regulation of glucose homeostasis.

Isolated fresh islets of Langerhans from rats of each group displayed an increased glucose stimulated insulin secretion as a percentage of glucose concentration in the media (Fig. 1A). There were no differences between experimental groups when the rats were incubated with 3.3 mM glucose. Islets harvested from YM rats released significantly higher amounts of insulin when stimulated with 16.7 mM glucose compared to control animals (Fig. 1A). They observed significant increases in IRS-1 and PI3K (p110 catalytic subunit) mRNA when islets were isolated from YM rats (Fig. 1C, E). There were no significant differences between any group in insulin receptor and IRS-2 mRNA levels (Fig. 1B, D). Figure 2 shows that insulin secretion by pancreatic islets was dose-dependent upon addition of glucose in all experimental conditions. When incubated with basal glucose concentration (3.3 mM), islets treated with Yerba mate freeze-dried extract or the phenolic compounds released similar amounts of insulin as compared to control. However, at high glucose concentration (16.7 mM), insulin secretion was significantly higher when incubated with 100 µg/mL YM freeze-dried extract, 1 µM chlorogenic acid, 0.1 and 1 µM rutin, 1 µM caffeic acid or 1 µM quercetin as compared to control conditions (Fig. 2).

Insulin secretion in response to different glucose concentration and mRNA levels of intracellular mediators of insulin signaling pathway.

Fig. 1. Insulin secretion in response to different glucose concentration and mRNA levels of intracellular mediators of insulin signaling pathway (Maiztegui B, Villagarcía HG, et al., 2023).

In vitro glucose-stimulated insulin release in presence of phenolic compounds of Yerba mate.

Fig. 2. In vitro glucose-stimulated insulin release in presence of phenolic compounds of Yerba mate (Maiztegui B, Villagarcía HG, et al., 2023).

Ask a Question

Write your own review

For research use only. Not for any other purpose.

Hot Products