Key result
Experimental diabetes doubles small intestine blood flow compared to controls at 4 weeks.
Why the study?
Alterations in blood flow distribution in experimental diabetes and their progression over time were not fully characterized.
Does streptozotocin-induced diabetes alter the distribution of cardiac output and regional blood flow in rats?
Does streptozotocin-induced diabetes alter the distribution of cardiac output and regional blood flow in rats?
Experimental diabetes in rats causes progressive alterations in regional blood flow, including a transiently increased cardiac index and subsequent decreased flow to skin and skeletal muscle, reflecting tissue adaptation to the metabolic disorder.
Answers are grounded in this paper and cite their sources.
May indicate splanchnic hyperperfusion in experimental diabetes; hypothesis-generating and leaves open human translation.
Alterations in blood flow distribution in streptozotocin-induced diabetes in the rat were examined. Blood flow between tissues was estimated by the distribution of radiolabeled microspheres, and a second series of experiments examined skeletal muscle microcirculation by in vivo microscopy. Studies were performed in anesthetized rats 1-8 wk after induction of diabetes. Cardiac index was transiently increased in diabetic animals (29.6 +/- 1.0 ml.min-1.100 g-1) in comparison with control animals (23.0 +/- 1.4 ml.min-1.100 g-1) at 2-wk duration. Cardiac index was similar in both groups of animals at all other time points studied. The increased cardiac index coincided with transiently increased blood flow to diaphragm and abdominal wall and a significant vasodilatation of small cremaster muscle arterioles. Blood flow to skin and some skeletal muscles was thereafter significantly decreased in the diabetic animals. Blood flow (ml.min-1.100 g-1) to the brain and main thoracic and abdominal organs was similar in nonfasting control and diabetic animals throughout the period of study. As a result of hyperplasia, blood flow to the small intestine (%cardiac output) was increased in the diabetic animals (at 4 wk of diabetes, 34.5 +/- 2.1 vs. 17.5 +/- 0.8%, P less than 0.001). Despite reduction in blood flow to the intestine, by dietary restriction, flow to skin and skeletal muscle remained significantly decreased. Insulin treatment, at a dose aimed at preventing body weight loss but maintaining hyperglycemia, led to renal hyperperfusion in comparison with untreated diabetic and control animals. The alterations in regional blood flow appear progressive in nature and are not simply related to each other but may reflect tissue adaptation to the metabolic disorder.
No takes yet. Share an insight, caveat, or question.
Hill et al. (1989) studied Streptozotocin-induced diabetes. Streptozotocin-induced diabetes vs. Control animals was evaluated on Blood flow to the small intestine (% cardiac output) at 4 weeks (p=<0.001). Streptozotocin-induced diabetes in rats significantly increased blood flow to the small intestine compared to controls at 4 weeks (34.5% vs. 17.5% of cardiac output, P<0.001).
Synapse has enriched 10 related papers. Consider them for comparative context: