PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
December 22, 2005European Journal of Clinical Investigation32 citations

Arterial stiffening and cardiac hypertrophy in a new rat model of type 2 diabetes

View Full Paper
KCKuo‐Chu ChangCTC D TsengTCTsai‐Fwu Chou

Structured PICO

Does induction of type 2 diabetes with streptozotocin and nicotinamide cause arterial stiffening and cardiac hypertrophy in male Wistar rats?

P
Population
Male Wistar rats at 2 months of age
I
Intervention
Streptozotocin (50 mg/kg IV) and nicotinamide (180 mg/kg IP) to induce type 2 diabetes, evaluated at 4 weeks and 8 weeks
C
Comparator
Untreated age-matched controls
O
Outcome
Haemodynamic parameters describing arterial wall elasticity and cardiac hypertrophy (aortic impedance analysis)surrogate

In a rat model of type 2 diabetes, 8 weeks of disease duration leads to significant arterial stiffening and increased wave reflection, which may contribute to increased left ventricular systolic load and subsequent cardiac hypertrophy.

Abstract

BACKGROUND: We determined the effects of NIDDM on haemodynamic parameters describing arterial wall elasticity and cardiac hypertrophy in rats administered streptozotocin (STZ) and nicotinamide (NA), using the aortic impedance analysis. METHODS: Male Wistar rats at 2 months were administered intraperitoneally 180 mg kg(-1) of NA, 30 min before an intravenous injection of 50 mg kg(-1) STZ, to induce type 2 diabetes. The STZ-NA rats were divided into two groups, 4 weeks and 8 weeks after induction of diabetes, and compared with untreated age-matched controls. Pulsatile aortic pressure and flow signals were measured by a high-fidelity pressure sensor and electromagnetic flow probe, respectively, and were then subjected to Fourier transformation for the analysis of aortic input impedance. RESULTS: In each diabetic group, the experimental syndrome was characterized by a moderate and stable hyperglycaemia and a relative deficiency of insulin secretion. However, the 8-week but not the 4-week STZ-NA diabetic rats showed a decrease in cardiac output in the absence of any significant changes in mean aortic pressure, having increased total peripheral resistance. The diabetic syndrome at 8 weeks also contributed to an increase in aortic characteristic impedance, from 1.49 +/- 0.33 (mean +/- SD) to 1.95 +/- 0.28 mmHg s mL(-1) (P < 0.05), suggesting a detriment to the aortic distensibility in NIDDM. Meanwhile, the STZ-NA diabetic animals after 8 weeks had an increased wave reflection factor (0.46 +/- 0.09 vs. 0.61 +/- 0.13, P < 0.05) and decreased wave transit time (25.8 +/- 3.8 vs. 20.6 +/- 2.8 ms, P < 0.05). Ratio of the left ventricular weight to body weight was also enhanced in the 8-week STZ-NA diabetic rats. CONCLUSION: The heavy intensity with early return of the pulse wave reflection may augment systolic load of the left ventricle coupled to the arterial system, leading to cardiac hypertrophy in the rats at 8 weeks after following STZ and NA administration.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Chang et al. (2005) studied this question.

synapsesocial.com/papers/6a70c9c4e71d69abee08d9f0https://doi.org/10.1111/j.1365-2362.2006.01588.x
Ask AI
Helpful
Bookmark
Share
View Full Paper