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Effects of renin-angiotensin system blockade on the islet morphology and function in rats with long-term high-fat diet.
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- Author(s): Yuan L;Yuan L; Li X; Li J; Li HL; Cheng SS
- Source:
Acta diabetologica [Acta Diabetol] 2013 Aug; Vol. 50 (4), pp. 479-88. Date of Electronic Publication: 2010 Jul 14.- Publication Type:
Journal Article; Research Support, Non-U.S. Gov't- Language:
English - Source:
- Additional Information
- Source: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9200299 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-5233 (Electronic) Linking ISSN: 09405429 NLM ISO Abbreviation: Acta Diabetol Subsets: MEDLINE
- Publication Information: Publication: Berlin : Springer Verlag
Original Publication: Berlin : Springer International, c1991- - Subject Terms: Diabetes Mellitus, Type 2/*drug therapy ; Diabetes Mellitus, Type 2/*metabolism ; Ion Channels/*metabolism ; Islets of Langerhans/*drug effects ; Mitochondrial Proteins/*metabolism ; Perindopril/*administration & dosage ; Renin-Angiotensin System/*drug effects; Animals ; Apoptosis/drug effects ; Benzimidazoles/administration & dosage ; Benzoates/administration & dosage ; Blood Glucose/metabolism ; Caspase 3/metabolism ; Diabetes Mellitus, Type 2/genetics ; Diabetes Mellitus, Type 2/physiopathology ; Diet, High-Fat/adverse effects ; Glucose Tolerance Test ; Humans ; Insulin/metabolism ; Insulin Secretion ; Interleukin-1beta/metabolism ; Ion Channels/genetics ; Islets of Langerhans/anatomy & histology ; Islets of Langerhans/cytology ; Islets of Langerhans/metabolism ; Male ; Mitochondrial Proteins/genetics ; Rats ; Rats, Wistar ; Telmisartan ; Uncoupling Protein 2
- Abstract: The renin-angiotensin system (RAS) has an important role in the endocrine pancreas. Multiple researches have shown that even in the insulin resistance phase, there are many abnormalities in islets morphology and function. This study aimed at investigating the effects of RAS blockade on the islets function in rats with long-term high-fat diet and its mechanisms. Wistar rats with 16-week high-fat diet were randomly divided into perindopril intervention group (FP, n = 15) and telmisartan intervention group (FT, n = 15). After 8-week intervention, insulin sensitivity and islets function were detected by hyperinsulinemic euglycemic clamp and intravenous glucose tolerance test (IVGTT), respectively. The pancreases were stained by immunohistochemistry technique to qualitatively and/or quantitatively analyze the relative content of insulin (IRC), NF-KB, uncoupling protein 2 (UCP2) and caspase-3 in islets. The apoptosis of islet cells was detected by TUNEL. The expression of angiotensin II receptor 1 (AT1R), interleukin-1β (IL-1β), hypoxia-inducing factor (HIF)-1α and CHOP mRNA in the islets was detected by reverse transcription polymerase chain reaction (RT-PCR). Compared with normal control group (NC, n = 15), the glucose infusion rate (GIR), area under the insulin curve (AUCI) of 0-10 min and IRC were decreased in high-fat control group (FC, n = 15). The relative content of NF-KB, UCP-2 and caspase-3 was increased significantly with the increased number of apoptotic cells in unit islets area. The relative expression of AT1R, IL-1β, HIF-1α and CHOP was also increased evidently (all P < 0.01). After intervention, the GIR, AUCI of 0-10 min and IRC were all increased obviously with the decreased relative concentration of NF-KB, UCP-2, caspase-3 and the number of apoptotic cell in unit islets area. The relative expression of AT1R, IL-1β, HIF-1α and CHOP mRNA was reduced significantly (all P < 0.01 or P < 0.05). There were no significant differences between groups FP and FT. So we concluded that blockade of RAS may protect islet function of rats with long-term high-fat diet via downregulation of islets inflammation, oxidative stress, endoplasmic reticulum stress and apoptosis, which have tight relationship with each other.
- Accession Number: 0 (Benzimidazoles)
0 (Benzoates)
0 (Blood Glucose)
0 (Insulin)
0 (Interleukin-1beta)
0 (Ion Channels)
0 (Mitochondrial Proteins)
0 (UCP2 protein, human)
0 (Ucp2 protein, rat)
0 (Uncoupling Protein 2)
EC 3.4.22.- (Caspase 3)
U5SYW473RQ (Telmisartan)
Y5GMK36KGY (Perindopril) - Publication Date: Date Created: 20100715 Date Completed: 20140519 Latest Revision: 20181217
- Publication Date: 20221213
- Accession Number: 10.1007/s00592-010-0210-8
- Accession Number: 20628770
- Source:
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