HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Telmisartan provides better renal protection than valsartan in a rat model of metabolic syndrome.

AbstractBACKGROUND:
Angiotensin receptor blockers (ARB), telmisartan, and valsartan were compared for renal protection in spontaneously hypertensive rats (SHR) fed high fat diet. We hypothesized that in cardiometabolic syndrome, telmisartan an ARB with peroxisome proliferators activated receptor-γ (PPAR-γ) activity will offer better renal protection.
METHODS:
SHR were fed either normal (SHR-NF, 7% fat) or high fat (SHR-HF, 36% fat) diet and treated with an ARB for 10 weeks.
RESULTS:
Blood pressure was similar between SHR-NF (190 ± 3 mm Hg) and SHR-HF (192 ± 4 mm Hg) at the end of the 10 week period. Telmisartan and valsartan decreased blood pressure to similar extents in SHR-NF and SHR-HF groups. Body weight was significantly higher in SHR-HF (368 ± 5 g) compared to SHR-NF (328 ± 7 g). Telmisartan but not valsartan significantly reduced the body weight gain in SHR-HF. Telmisartan was also more effective than valsartan in improving glycemic and lipid status in SHR-HF. Monocyte chemoattractant protein-1 (MCP-1), an inflammatory marker, was higher in SHR-HF (24 ± 2 ng/d) compared to SHR-NF (14 ± 5 ng/d). Telmisartan reduced MCP-1 excretion in both SHR-HF and SHR-NF to a greater extent than valsartan. An indicator of renal injury, urinary albumin excretion increased to 85 ± 8 mg/d in SHR-HF compared to 54 ± 9 mg/d in SHR-NF. Telmisartan (23 ± 5 mg/d) was more effective than valsartan (45 ± 3 mg/d) in lowering urinary albumin excretion in SHR-HF. Moreover, telmisartan reduced glomerular damage to a greater extent than valsartan in the SHR-HF.
CONCLUSIONS:
Collectively, our data demonstrate that telmisartan was more effective than valsartan in reducing body weight gain, renal inflammation, and renal injury in a rat model of cardiometabolic syndrome.
AuthorsAbdul Hye Khan, John D Imig
JournalAmerican journal of hypertension (Am J Hypertens) Vol. 24 Issue 7 Pg. 816-21 (Jul 2011) ISSN: 1941-7225 [Electronic] United States
PMID21415842 (Publication Type: Comparative Study, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Angiotensin II Type 2 Receptor Blockers
  • Benzimidazoles
  • Benzoates
  • Dietary Fats
  • PPAR gamma
  • Tetrazoles
  • Valsartan
  • Valine
  • Telmisartan
Topics
  • Angiotensin II Type 2 Receptor Blockers (pharmacology, therapeutic use)
  • Animals
  • Benzimidazoles (pharmacology, therapeutic use)
  • Benzoates (pharmacology, therapeutic use)
  • Blood Pressure (drug effects, physiology)
  • Body Weight (drug effects, physiology)
  • Dietary Fats (adverse effects)
  • Disease Models, Animal
  • Hypertension (drug therapy, physiopathology)
  • Kidney Diseases (physiopathology, prevention & control)
  • Male
  • Metabolic Syndrome (chemically induced, physiopathology)
  • PPAR gamma (physiology)
  • Rats
  • Rats, Inbred SHR
  • Telmisartan
  • Tetrazoles (pharmacology, therapeutic use)
  • Treatment Outcome
  • Valine (analogs & derivatives, pharmacology, therapeutic use)
  • Valsartan

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: