10 April 2013: Clinical Research
What is more damaging to vascular endothelial function: Diabetes, age, high BMI, or all of the above?
Jerrold Scott Petrofsky ABCDEF , Faris Alshammari ABCDF , Gurinder Singh Bains ABCDEF , Iman Akef Khowailed ABCDEF , Haneul Lee ABCD , Yashvanth Nagarajamurthy Kuderu ABCD , Riya D. Lodha ABCD , Sophia Rodrigues ABCD , Diamond Nguyen BCD , Pooja Ashok Potnis BCD , Pooja P. Deshpande BCD , Jong Eun Yim ABCDEF , Lee Berk ABCDEF
DOI: 10.12659/MSM.883878
Med Sci Monit 2013; 19:257-263
Abstract
BACKGROUND: It is well established that there is a reduction in the skin blood flow (SBF) in response to heat with age and diabetes. While it is known that high BMI creates a stress on the cardiovascular system and increases the risk of all cause of morbidity and mortality, little is known of the effect of high BMI on SBF response to heat. Since diabetes is associated with age and a higher BMI, the interrelationship between age, BMI and SBF needs to be investigated to better understand the contribution diabetes alone has to endothelial impairment.
MATERIAL AND METHODS: This study examined the SBF to heat in young and old people with low and high BMI and people with diabetes with high BMI to determine the contribution these variables have on SBF. Subjects were ten young and older people with BMI <20 and ten young and older people with BMI >20 and ten subjects with diabetes with BMI >20. The SBF response, above the quadriceps, was determined during a 6 minutes exposure to heat at 44°C.
RESULTS: Even in young people, SBF after the stress of heat exposure was reduced in subjects with a high BMI. The effect of BMI was greatest in young people and lowest in older people and people with diabetes; in people with diabetes, BMI was a more significant variable than diabetes in causing impairment of blood flow to heat. BMI, for example, was responsible for 49% of the reduction in blood flow after stress heat exposure (R=–0.7) while ageing only accounted for 16% of the blood flow reduction (R=–0.397).
CONCLUSIONS: These results would suggest the importance of keeping BMI low not only in people with diabetes to minimize further circulatory vascular damage, but also in young people to diminish long term circulatory vascular compromise.
Keywords: Muscles - physiopathology, Endothelium, Vascular - physiopathology, Diabetes Mellitus - physiopathology, Body Mass Index, Aging - pathology, Adolescent, Skin - physiopathology, Skin Temperature, young adult
Background
The use of heat for both therapeutic and preventive purposes dates back to 124 BC with the introduction by Asclepiads, a Greek physician [1]. Temperature is sensed in blood vessels through the TRP receptors and transient receptor potential channels, or TRP channels, are responsible for managing the body’s response to various stimuli, such as change in temperature [2–6]. One type of TRP channel is the TRPV channel, in which the V stands for vanilloid [6–10]. All TRPV1–4 channels are non-selective cation channels, moderately permeable to calcium, and are temperature sensitive [6,10–15].
TRPV1 was first isolated and named in 1997 as a capsaicin receptor [16–18]. It has been found that TRPV1 is found in greatest number in sensory neurons. TRPV1 is a heat sensor, and is activated by heat, specifically temperatures >42°C [16,18–20]. TRPV4 is expressed in epidermal keratinocytes [15]. While TRPV4 can be activated by warmth, it can also be activated by hypo-osmolarity [18,21–23].
The mechanism of the response of heat is two-fold. When skin is exposed to a temperature above 42°C, there is an immediate increase in circulation, controlled by sensory nerves in the skin [24–26]. This is mediated by TRPV1 calcium channels increasing calcium permeability, which then causes neuropeptides to be released, resulting in vasodilatation from the relaxation of smooth muscle [27–29]. This vasodilatation occurs to protect the skin in the event of a rapid change in temperature that may damage the skin [30–32]. Prolonged vasodilatation with exposure to heat occurs due to the influx of calcium and activation of nitric oxide synthetase mediated by TRPV4 channels on vascular endothelial cells [24–26].
The blood flow response to heat is impaired with ageing and diabetes [33–35]. While this is well documented, much less is known about the blood flow response to free radicals. When the free radical concentration reaches a critical level, rather than increasing blood flow, they biodegrade nitric oxide and prostacyclin, a second vasodilator released from vascular endothelial cells, into inactive forms [36–38]. In the presence of free radicals such as hydrogen peroxide, nitric oxide is reduced to peroxynitrite (ONOO), a free radical with no influence on circulation [39]. Bioconversion of nitric oxide to peroxynitrite is believed to be one of the mechanisms associated with the reduction in circulation at rest and during stress in older people and people with diabetes and leads to endothelial dysfunction [39]. In a recent study, free radicals were elevated in Asians after a single high fat meal. This resulted in a diminished blood flow response to heat [40,41]. Free radicals are also very high in people who are overweight [42,43]. If BMI itself limits the blood flow response to stress such as heat due to high free radicals in the body, and most people with diabetes have a high BMI, some of the damage from diabetes to circulation may be due to the BMI and not diabetes itself. The purpose of the present investigation was to test the hypothesis that high BMI in itself in addition to age are the main elements causing reduced blood flow in people with diabetes. Young and old subjects with low and high BMI were examined and their response to heat was measured. These data were used to establish a multifactor regression equation to predict what blood flow should be in people with diabetes based on their age and BMI. By comparing this to the actual blood flow response to heat, the reduction in blood flow due to diabetes alone could be calculated
Material and Methods
MEASUREMENT OF SKIN TEMPERATURE:
Skin temperature was measured with a thermistor (SKT RX 202A) manufactured by BioPac systems (BioPac Inc., Goleta, CA). The thermistor output was sensed by an SKT 100 thermistor amplifier (BioPac Inc., Goleta, CA). The output, which was a voltage between 0 and 10 volts, was then sampled with an analog to digital converter at a frequency of a 1,000 samples per second with a resolution of 24 bits with a BioPac MP150 analog to digital converter. The converted data was then stored on a desk top computer using Acknowledge 4.1 software for future analysis. Data analysis was done over a 5 second period for mean temperature. The temperature was calibrated at the beginning of each day by placing the thermistors used in the study in a controlled temperature water bath which will be calibrated against a standard thermometer.
MEASUREMENT OF SKIN BLOOD FLOW:
Skin blood flow was measured with a Moor Laser Doppler flow meter (VMS LDF20, Oxford England). The imager uses a red laser beam (632.8 nm) to measure skin blood flow using the Doppler Effect. After warming the laser for 15 to 30 minutes prior to use, the laser was applied to the skin through a fiber optic probe placed above the knee on the quadriceps (Figure 1). The probe was a VP12B. The Moor Laser Doppler flow meter measures blood flow through most of the dermal layer of the skin but does penetrate the entire dermal layer. Blood flow is then calculated in a unit called Flux based on the red cell concentration in red cell velocity with a stated accuracy of ±10%. The tissue thickness sampled is typically 1mm in depth.
CONTROL OF SKIN TEMPERATURE:
Skin temperature was controlled by a Moor temperature controller (SH02) with an SHO2-SHP1 skin temperature module which integrated with the blood flow fiber optic probe also shown in Figure 1. This is a closed loop electric warmer (thermode) where temperature is controlled to 0.1°C.
MEASUREMENT OF THE RESPONSE TO HEAT:
The response of the skin to heat was measured by applying the heated probe to the skin for 6 minutes. The thermode was set at a temperature of 44°C. This warmed the skin and blood flow was then recorded.
PROCEDURES:
Subjects were interviewed for inclusion and exclusion criteria. Those subjects that were eligible were placed into the study and read and signed a statement of informed consent. Next, subjects rested for 15 minutes while height and weight were taken. Baseline skin blood flow was recorded for 1 minute over the quadriceps. After this period of time, the thermode was applied upon the leg above the belly of the quadriceps muscle to warm the skin to 44°C. The thermode was left on for 6 minutes.
STATISTICAL ANALYSIS:
Data was summarized as means and standard deviations. For comparison, T test, ANOVA and multiple regression and correlations were calculated. The level of significance was set at p=0.05.
Results
The results for the young subjects with low and high BMI are shown in Figure 1. As shown for the entire young group, blood flow increased slowly at first and then exponentially during the 6 minute heat exposure. However, the blood flow after 1 minute 15 seconds and until the end of the experiment was greater in the low BMI group than the high BMI group (ANOVA p<0.05). From 1 minute 30 seconds to 3 minutes, the slope of the increase in blood flow per minute was the same in both groups of subjects but the magnitude of the increase was less in the low BMI young group (slope difference was p>0.05). As an index of the blood flow increase during heat exposure, the total increase in blood flow above the resting blood flow in the last 5 minutes of heat exposure was calculated in this and all groups of subjects. For the younger group, the correlation between BMI and blood flow during the last 5 minutes of heat exposure was −0.64, a significant correlation (p<0.01) showing that blood flow was reduced as a function of BMI.
The same was true of the older group (Figure 2). The high BMI older group had a significant impairment in the blood flow response to heat after the first minute that heat was applied. Resting blood flow was not different in the low and high BMI groups (p>0.05). However, after heat was applied, there was a large difference between these groups. As was seen with the younger group, in the older group, there was a significant negative correlation between BMI and blood flow during the last 5 minutes of heat exposure. The correlation here was −0.73, a significant negative correlation (p<0.01).
The blood flow during heat exposure was significantly higher in the high BMI younger group than the high BMI older group (p<0.05). Young and old high BMI groups were also significantly different from each other (p<0.05) but the younger group had greater blood flows during heat than that seen in the older group (p<0.05). Thus both ageing and BMI contributed to a lower blood flow response in the last 5 minutes of heat stress.
This relationship is shown in the scatter diagram in Figure 3. It is a scatter diagram showing all data on the young and old subjects pooled together. The regression equation in the figure shows that BMI had a more significant effect on reducing the blood flow response to heat than did ageing. The multiple correlation coefficients for age and BMI and blood flow showed the correlation with age was −0.397 and for BMI was −0.70. The R2 therefore showed that about 16% of the loss in circulation was due to age and 49% due to high BMI. These correlations were both significant (p<0.01). Using the regression equation, blood flow in the last 5 minutes of heat exposure was measured in the 10 subjects as an average of 178.4 flux in the young low BMI group as would be predicted by the regression equation in Figure 3 to be 164.1 flux. For the young high BMI group, the actual blood flow measured on the 10 subjects was an average of 94.1 flux and was predicted by the regression equation to be 96.0 flux. For the older low BMI group the actual blood flow measured on the 10 subjects averaged 115.2 flux and was predicted by the regression equation to be 116.1 flux in the last 5 minutes after heat exposure. For the old high BMI group, the actual blood flow for the 10 subjects was an average of was 49.3 flux and was predicted by the regression equation to be 49.2 flux. Thus the regression equation was highly predicative of the results seen in these experiments. For the subjects with diabetes, the blood flows were even lower in response to heat. We could not find low BMI subjects with diabetes and therefore only a high BMI group is shown. As can be seen here, diabetes in itself reduced blood flow even further (Figure 4) for subjects at the same BMI and age as in Figure 2. However, when using the subject’s age and BMI, the equation in Figure 3 predicts the blood flow in the last 5 minutes should be 47.3 flux whereas the actual blood flow in the last 5 minutes averaged, for the 10 subjects in this group, 37.1 flux. The difference is small and supports the idea that only about 20% of the lower blood flow response to heat is due to diabetes itself. The majority of the lower blood flow response to heat is due to high BMI and ageing.
Discussion
Recent studies have shown that a Westernized diet in Asians reduces the skin blood flow in response to heat stress and occlusion due to high concentration of free radicals in blood from the type of fat in the diet [41,44]. Administration of antioxidants reversed this impairment even after high fat meals [44–46]. It is also well established that high concentrations of blood born free radicals are found in people with high BMI’s [36,47,48]. As people age and especially in people with diabetes, BMI is elevated. And yet, no study has examined the interrelationship between BMI and blood flow in response to stressors such as heat. Since free radicals are high in older people and people who have diabetes, it might be anticipated that diabetes and ageing would have some impact through these free radicals in the blood thereby reducing endothelial function [25,26,42]. Thus the purpose of the present research study was to examine how much reduction in endothelial function was there in people with diabetes: 1) that was due to ageing and, 2) how much was due to BMI and, 3) how much is due to diabetes itself.
The results presented here would appear to confirm this hypothesis. Even young subjects had a reduced blood flow response to heat stress if they had a high BMI. In subjects who had diabetes, we were not able to find a low BMI group. However, for this group of subjects, the differential effects of age and diabetes could be deduced by examining the age matched controls. When the contributions of age and BMI are eliminated from the blood flow response to heat stress, BMI, and diabetes are not equal contributors to impaired endothelial function. By and large, BMI appears to be the major contributor to endothelial dysfunction, ageing contributes a small amount, and the remainder appears to be due to diabetes and poor glycemic control.
Suggested ways to reduce this endothelial damage is a lifestyle change with an increase in exercise and a reduction of body weight [49]. Exercise has been shown to increase free radicals during the actual exercise but, with training, appears to optimize the immune response, thereby, producing an overall reduction in body inflammation [49]. Another approach would be to increase the intake of antioxidants. This has been shown to increase blood flow to tissue in even a young population [46,50,51]. However, this is especially true and significant with high fat diets in populations such as Asians who have a poor tolerance for high fat foods and thus produce free radicals after even a single high fat meal [40,46,51]. When Asians took antioxidants there was an increase in their blood flow in response to heat stress and occlusion in spite of the high fat meal [44]. Also, even a simple change in diet, for example, drinking green tea or taking green tea extract has been shown to reduce cellular inflammation by blocking the activation of NFKb, the nuclear sub transmitter that activates inflammation in cells[52,53]. In addition, there are also many other sources of free radical scavengers in the diet.
However, it should be stated that free radicals are also used for cellular communication, including in muscle during exercise [54]. Red blood cells release nitric oxide (a fee radical) to increase the diameter of arteries if they encounter high shear stresses [55]. Endothelial cells release nitric oxide in response to heat and other stressors to increase circulation [50]. The mitochondria in muscle release nitric oxide to increase energy delivery to the cell through increased blood flow if the mitochondria are active [48,49]. Thus, free radicals are critical for cell function. Therefore, an overdose of anti-oxidants such as vitamins A, C and E can impair exercise performance [56]. Thus the dosage of antioxidants must be given in response to the excess free radicals found in the body. For even young people with a high BMI, one dose is needed in the diet or with supplements of antioxidants while for people with diabetes and those who have high BMI and who are older, a much greater dosage should be considered for every day. This would explain various studies showing no effect of antioxidants in younger people who are thin but increased endothelial function in younger people with a high BMI. Endothelial function in older people also seems to improve with antioxidant dosage, again supporting this hypothesis that it is free radicals that reduce endothelial function [57]. Further research needs to be conducted on the dosage
References
1. van Tubergen A, van der Linden S, A brief history of spa therapy: Ann Rheum Dis, 2002; 61(3); 273-75, pmid: 11830439
2. McKemy DD, Neuhausser WM, Julius D, Identification of a cold receptor reveals a general role for TRP channels in thermosensation: Nature, 2002; 416(6876); 52-58, pmid: 11882888
3. Peier AM, A TRP channel that senses cold stimuli and menthol: Cell, 2002; 108(5); 705-15, pmid: 11893340
4. Reid G, ThermoTRP channels and cold sensing: what are they really up to?: Pflugers Arch, 2005; 451(1); 250-63, pmid: 16075243
5. Voets T, Sensing with TRP channels: Nat Chem Biol, 2005; 1(2); 85-92, pmid: 16408004
6. Mergler S, Thermosensitive transient receptor potential channels (thermo-TRPs) in human corneal epithelial cells: J Cell Physiol; 2010
7. Owsianik G, Permeation and selectivity of TRP channels: Annu Rev Physiol, 2006; 68; 685-717, pmid: 16460288
8. Pedersen SF, Owsianik G, Nilius B, TRP channels: an overview: Cell Calcium, 2005; 38(3–4); 233-52, pmid: 16098585
9. Ramsey IS, Delling M, Clapham DE, An introduction to TRP channels: Annu Rev Physiol, 2006; 68; 619-47, pmid: 16460286
10. Nilius B, Transient receptor potential cation channels in disease: Physiol Rev, 2007; 87(1); 165-217, pmid: 17237345
11. Venkatachalam K, Montell C, TRP channels: Annu Rev Biochem, 2007; 76; 387-417, pmid: 17579562
12. Benham CD, Davis JB, Randall AD, Vanilloid and TRP channels: a family of lipid-gated cation channels: Neuropharmacology, 2002; 42(7); 873-88, pmid: 12069898
13. Nilius B, TRPV4 calcium entry channel: a paradigm for gating diversity: Am J Physiol Cell Physiol, 2004; 286(2); C195-205, pmid: 14707014
14. Nilius B, Watanabe H, Vriens J, The TRPV4 channel: structure-function relationship and promiscuous gating behaviour: Pflugers Arch, 2003; 446(3); 298-303, pmid: 12715179
15. Everaerts W, Nilius B, Owsianik G, The vanilloid transient receptor potential channel TRPV4: from structure to disease: Prog Biophys Mol Biol, 2010; 103(1); 2-17, pmid: 19835908
16. Caterina MJ, The capsaicin receptor: a heat-activated ion channel in the pain pathway: Nature, 1997; 389(6653); 816-24, pmid: 9349813
17. Caterina MJ, Julius D, The vanilloid receptor: a molecular gateway to the pain pathway: Annu Rev Neurosci, 2001; 24; 487-517, pmid: 11283319
18. Tominaga M: The Role of TRP Channels in Thermosensation, 2007
19. Tominaga M, The cloned capsaicin receptor integrates multiple pain-producing stimuli: Neuron, 1998; 21(3); 531-43, pmid: 9768840
20. Cesare P, Specific involvement of PKC-epsilon in sensitization of the neuronal response to painful heat: Neuron, 1999; 23(3); 617-24, pmid: 10433272
21. Liedtke W, Vanilloid receptor-related osmotically activated channel (VR-OAC), a candidate vertebrate osmoreceptor: Cell, 2000; 103(3); 525-35, pmid: 11081638
22. Strotmann R, OTRPC4, a nonselective cation channel that confers sensitivity to extracellular osmolarity: Nat Cell Biol, 2000; 2(10); 695-702, pmid: 11025659
23. Wissenbach U, Trp12, a novel Trp related protein from kidney: FEBS Lett, 2000; 485(2–3); 127-34, pmid: 11094154
24. Kellogg DL, Role of nitric oxide in the vascular effects of local warming of the skin in humans: J Appl Physiol, 1999; 86(4); 1185-90, pmid: 10194201
25. Minson CT, Berry LT, Joyner MJ, Nitric oxide and neurally mediated regulation of skin blood flow during local heating: J Appl Physiol, 2001; 91(4); 1619-26, pmid: 11568143
26. Minson CT, Decreased nitric oxide- and axon reflex-mediated cutaneous vasodilation with age during local heating: J Appl Physiol, 2002; 93(5); 1644-49, pmid: 12381749
27. Namer B, Chemically and electrically induced sweating and flare reaction: Auton Neurosci, 2004; 114(1-2); 72-82, pmid: 15331047
28. Petrofsky JS, Al-Malty AM, Prowse M, Relationship between multiple stimuli and skin blood flow: Med Sci Monit, 2008; 14(8); CR399-405, pmid: 18667996
29. Sauerstein K, Electrically evoked neuropeptide release and neurogenic inflammation differ between rat and human skin: J Physiol, 2000; 529; 803-10, pmid: 11118507
30. Almalty AM, An effective method for skin blood flow measurement using local heat combined with electrical stimulation: J Med Eng Technol, 2009; 33(8); 663-69, pmid: 19848861
31. Rowell LB, Human cardiovascular adjustments to exercise and thermal stress: Physiol Rev, 1974; 54(1); 75-159, pmid: 4587247
32. Rowell LB, Reflex control of the cutaneous vasculature: J Invest Dermatol, 1977; 69(1); 154-66, pmid: 326990
33. Petrofsky J, The interrealtionship between locally applied heat, ageing and skin blood flow on heat transfer into and from the skin: J Med Eng Technol, 2011; 35(5); 262-74, pmid: 21605003
34. Petrofsky J, The ability of different areas of the skin to absorb heat from a locally applied heat source: the impact of diabetes: Diabetes Technol Ther, 2011; 13(3); 365-72, pmid: 21291332
35. Petrofsky J, The ability of the skin to absorb heat; the effect of repeated exposure and age: Med Sci Monit, 2011; 17(1); CR1-8, pmid: 21169905
36. Vecchini A, Dietary alpha-linolenic acid reduces COX-2 expression and induces apoptosis of hepatoma cells: J Lipid Res, 2004; 45(2); 308-16, pmid: 14563831
37. Wong BJ, Fieger SM, Transient receptor potential vanilloid type-1 (TRPV-1) channels contribute to cutaneous thermal hyperaemia in humans: J Physiol, 2010; 588(Pt 21); 4317-26, pmid: 20807792
38. Petrofsky J, Dry heat, moist heat and body fat: are heating modalities really effective in people who are overweight?: J Med Eng Technol, 2009; 33(5); 361-69, pmid: 19499453
39. Farage M, Miller K, Maibach H: Influence of Race, Gender, Age and Diabetes on the Skin Circluation Text Book of Ageing Skin, 2010, Berlin Heidelberg, Springer
40. Bui C, Acute effect of a single high-fat meal on forearm blood flow, blood pressure and heart rate in healthy male Asians and Caucasians: a pilot study: Southeast Asian J Trop Med Public Health, 2010; 41(2); 490-500, pmid: 20578534
41. Yim J, Differences in endothelial function between Korean-Asians and Caucasians: Med Sci Monit, 2012; 18(6); CR337-43, pmid: 22648248
42. Calder PC, Dietary factors and low-grade inflammation in relation to overweight and obesity: Br J Nutr, 2011; 106(Suppl 3); S5-78, pmid: 22133051
43. de Heredia FP, Gomez-Martinez S, Marcos A, Obesity, inflammation and the immune system: Proc Nutr Soc, 2012; 71(2); 332-38, pmid: 22429824
44. Yim J, Protective effect of anti-oxidants on endothelial function in young Korean-Asians compared to Caucasians: Med Sci Monit, 2012; 18(8); CR467-79, pmid: 22847195
45. Practical study of the establishment of menus in general hospital, with a view to a diet balanced and adapted to different categories of hospitalized patients: Terramycine Informations, 1960; 16; 49-52
46. Petrofsky JS, Laymon M, Lee H, The Effect of Coenzyme Q-10 on Endothelial Function in a Young Population: Physical Therapy Rehabilitation Science, 2012; 1; 6-12
47. Higdon JV, Frei B, Obesity and oxidative stress: a direct link to CVD?: Arterioscler Thromb Vasc Biol, 2003; 23(3); 365-67, pmid: 12639823
48. Middleton E, Kandaswami C, Theoharides TC, The effects of plant flavonoids on mammalian cells: implications for inflammation, heart disease, and cancer: Pharmacol Rev, 2000; 52(4); 673-751, pmid: 11121513
49. Powers SK, Jackson MJ, Exercise-induced oxidative stress: cellular mechanisms and impact on muscle force production: Physiol Rev, 2008; 88(4); 1243-76, pmid: 18923182
50. Petrofsky JS, Resting blood flow in the skin: does it exist, and what is the influence of temperature, aging, and diabetes?: J Diabetes Sci Technol, 2012; 6(3); 674-85, pmid: 22768900
51. Petrofsky JS, Reduced endothelial function in the skin in Southeast Asians compared to Caucasians: Med Sci Monit, 2012; 18(1); CR1-8, pmid: 22207113
52. Babu PV, Liu D, Green tea catechins and cardiovascular health: an update: Curr Med Chem, 2008; 15(18); 1840-50, pmid: 18691042
53. Babu PV, Sabitha KE, Shyamaladevi CS, Effect of green tea extract on advanced glycation and cross-linking of tail tendon collagen in streptozotocin induced diabetic rats: Food Chem Toxicol, 2008; 46(1); 280-85, pmid: 17884275
54. Powers SK, Talbert EE, Adhihetty PJ, Reactive oxygen and nitrogen species as intracellular signals in skeletal muscle: J Physiol, 2011; 589(Pt 9); 2129-38, pmid: 21224240
55. Baskurt OK, Ulker P, Meiselman HJ, Nitric oxide, erythrocytes and exercise: Clin Hemorheol Microcirc, 2011; 49(1–4); 175-81, pmid: 22214688
56. Peternelj TT, Coombes JS, Antioxidant Supplementation during Exercise Training: Beneficial or Detrimental?: Sports Med, 2011; 41(12); 1043-69, pmid: 22060178
57. Wray DW, Acute reversal of endothelial dysfunction in the elderly after antioxidant consumption: Hypertension, 2012; 59(4); 818-24, pmid: 22353612
58. Tare M, Vitamin D insufficiency is associated with impaired vascular endothelial and smooth muscle function and hypertension in young rats: J Physiol, 2011; 589(Pt 19); 4777-86, pmid: 21807617
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