- Open Access
Dietary potassium supplementation improves vascular structure and ameliorates the damage caused by cerebral ischemia in normotensive rats
© Rigsby et al; licensee BioMed Central Ltd. 2008
- Received: 06 July 2007
- Accepted: 31 January 2008
- Published: 31 January 2008
Dietary potassium supplementation in hypertensive rats is cardioprotective. This protection includes a blood pressure independent reduction in the amount of damage caused by cerebral ischemia. Therefore, we hypothesized that dietary potassium supplementation would improve the outcome of ischemic stroke by improving cerebral vessel structure in normotensive rats.
Wistar Kyoto (WKY) rats were fed a high (HK) or low potassium (LK) diet for six weeks from six weeks of age. At the end of treatment, cerebral ischemia was induced by middle cerebral artery (MCA) occlusion and the resultant infarct was quantified and expressed as a percentage of the hemisphere infarcted (%HI). MCA structure was assessed in an additional group of rats using a pressurized arteriograph.
The cerebral infarct was significantly smaller in rats fed the HK diet, compared to rats fed the LK diet (21 ± 5.4 vs 33.5 ± 4.8 %HI HK vs LK p < 0.05). Vessel structure was improved in WKY rats fed the HK diet as indicated by an increase in the MCA lumen (298 ± 6.3 vs 276 ± 3.9 μm HK vs LK p < 0.05) and outer diameters (322 ± 7.6 vs 305 ± 4.8 μm HK vs LK p < 0.05). Wall thickness and area were unchanged, suggesting an outward euthrophic remodelling process. The HK diet had no effect on body weight or telemetry blood pressure.
These studies are the first to show a beneficial effect of dietary potassium in rats with normal blood pressure.
- Cerebral Ischemia
- Middle Cerebral Artery
- Middle Cerebral Artery Occlusion
- Physiological Salt Solution
- Vessel Wall Thickness
Epidemiological studies show that potassium intake correlates inversely with the incidence of cerebrovascular events [1–4]. It has been clear for some time that a high potassium diet reduces the number of hemorrhagic strokes in stroke prone spontaneously hypertensive rats (SHRSP) [5, 6] and reduces the risk of stroke in humans [1–3]. We have also previously shown that administration of spironolactone, a potassium sparing drug, reduces the ischemic cerebral infarct size in SHRSP . We have recently shown that dietary potassium supplementation also reduces the size of ischemic cerebral infarcts in SHRSP and improves the structure of the MCA . Interestingly, dietary potassium supplementation did not alter blood pressure in the SHRSP fed a normal sodium diet. This presents the possibility that the effects of potassium supplementation are blood pressure independent and may also occur in normotensive rats.
Sixty to eighty percent of ischemic strokes can be attributed to hypertension . However, there remains a significant population that suffers from an ischemic stroke while their blood pressure is normal. It would therefore seem prudent to assess if therapies that have been shown to be beneficial in hypertensive rats can also reduce the ischemic damage in rats with normal blood pressure. Therefore we designed experiments to test the effects of a HK diet in normotensive WKY rats.
Male WKY rats were purchased from Harlan (Indianapolis IN). Rats were maintained on a 12-hour light dark cycle, housed two per cage and allowed access to food and water ad libitum. Rats were fed either a low potassium (LK) or a high potassium (HK) chow containing 0.79% and 2.11% potassium respectively (Zeigler Brothers: Gardners PA) from 6 to 12 weeks of age. Both the HK and LK diets contained 0.16% NaCl. These studies complied with the protocols for animal use outlined by the American Physiological Society and were approved by the Institutional Animal Care and Use Committee.
Rats were anesthetized with sodium pentobarbital (50 mg/kg IP) and body temperature was maintained at 37°C during anaesthesia. The MCA was permanently occluded using the intralumenal thread occlusion technique . Briefly, the common carotid artery was exposed by a midline incision and the branches of the external carotid artery were cauterized. A 3-0 monofilament thread with a rounded tip was introduced into the carotid artery and advanced cranially into the internal carotid artery over a distance of 19 mm, measured from the bifurcation of the common carotid artery. The thread was left in place and the rats were allowed to recover. Blood flow to the region surrounding the MCA was measured using a laser Doppler flow probe to confirm MCA occlusion. Post-occlusion (24 hours), the rats were anesthetized and decapitated and the brains carefully removed. The area of the infarction was quantified using 2,3,5-triphenyltetrazolium (TTC) staining as described previously. The area of the brain that stained pink in response to TTC was deemed to be viable tissue and the white area was classified as tissue damaged by ischemia .
MCAs were isolated and placed in cold physiological salt solution (PSS) (in mM: 141.9 NaCl, 4.7 KCl, 1.7 MgSO4, 0.5 EDTA, 2.8 CaCl2, 10.0 HEPES, 1.2 KH2PO4, and 5.0 glucose). The first branch-free segment of the MCA most proximal to the Circle of Willis was mounted on two glass micropipettes in a small vessel arteriograph (Living Systems Instrumentation, Burlington, VT). Vessels were bathed with warm oxygenated PSS and the intralumenal pressure was set at 75 mmHg before the vessels were allowed to equilibrate for 30 minutes. Vessels that did not hold pressure were discarded (vessels from 3 control rats were discarded for this reason). For the analysis of vessel structure, the vessels were bathed in calcium free PSS containing 2 mM EGTA and the intralumenal pressure was increased from 0 to 180 mmHg in 20 mmHg increments. Videomicroscopy was used to measure lumen diameter, external diameter and wall thickness at each pressure after a 5-minute equilibration. The wall/lumen ratio, circumferential wall stress, wall strain and distensibility were calculated using the method of Baumbach and Hadju (13). The vessel growth and remodelling indices were calculated for vessels at an intralumenal pressure of 80 mmHg using the formula described by Heagerty et al . The elastic modulus (β-coefficient) was calculated from the stress/strain curves for the individual vessels, these curves were fitted to an exponential model (y = aeβx) where β is the slope of the curve: the higher the β-coefficient the stiffer the vessel.
Blood pressure and plasma electrolytes
Blood pressure was continuously monitored by telemetry  (Data Sciences, Inc.; 20). Telemetry probes were placed in the abdominal aorta of five-week old rats. Baseline blood pressure was measured for 3 days before the animals were placed on the specialized diets at six week of age. Plasma sodium and potassium was measured using the Synchron EL-ISE electrolyte system (Beckman Instruments).
All general laboratory chemicals were purchased from Sigma (St. Louis MO).
All results are represented as a mean ± standard error of the mean. Cerebral vascular structure data and blood pressures were analyzed by two-way repeated measures ANOVA with a Bonferroni post-test. Cerebral infarct size, plasma electrolytes, body weights and β-coefficients were compared using Student's t-test. A p-value ≤ 0.05 was considered significant.
Blood pressure, plasma electrolytes and body weights
Cerebral infract size
Passive vessel dynamics
There are two novel findings in this study. First, we have shown that dietary potassium supplementation reduces the size of the ischemic cerebral infarct in normotensive rats. We have also shown that the MCAs from the rats fed the HK diet have larger lumen and outer diameters. Several studies have shown that reducing the lumen and outer diameters of the MCA reduces the vessels ability to autoregulate , and dilate , both of these effects may contribute to an increase in the amount of damage caused by cerebral ischemia. Therefore, by increasing the vessel diameters it is possible that the HK diet improved cerebral vessel function and that this is responsible for the reduction in the cerebral infarct size. To the best of our knowledge this is the first study to show a beneficial effect of dietary potassium supplementation in a normotensive rat.
In these studies the rats were fed the specialized diets for six weeks beginning at six weeks of age, this time frame was chosen to mimic the treatment regime used in our previous studies of the effects of dietary potassium supplementation in SHRSP . In that study we observed that dietary potassium supplementation reduced the ischemic cerebral infarct size and improved cerebral vessel structure in hypertensive rats. The results obtained in the current study suggest that potassium supplementation has a similar effect in normotensive rats. Interestingly, the pattern of changes in vessel structure is not the same in the SHRSP and WKY rats. In the SHRSP we observed no change in the lumen diameter of the MCA but reduction in the wall thickness and wall/lumen ratio . This suggests that in the hypertensive rats the HK diet is preventing vessel hypertrophy or hyperplasia. This was not the case in the WKY rats, here the changes in vessel structure with dietary potassium supplementation appear to reflect an outward euthrophic remodeling process, or a increase in the vessel size without a change in the wall thickness, this is supported by the calculations of the remodeling and growth indices. Why the hypertensive rats and normotensive rats respond differently to the HK diet remains unclear. It is possible that the difference in blood pressure between the two strains is responsible for the different responses. Also, in the SHRSP the HK diet caused a significant increase in the plasma potassium concentrations, while there was a trend towards an increase in the WKY rats it did not reach statistical significance. This raises the possibility that there are differences in the potassium handling between the two strains and that may be responsible for the difference in the effect.
The mechanism for the effect of the HK diet on vascular structure in the WKY rats remains unclear. Our previous studies using SHRSP showed that the mRNA levels of various growth factor receptors and collagens were reduced by the HK diet . Because we do not observe a change in vessel wall thickness in the WKY rats it seems unlikely that the HK diet is preventing growth factor stimulated smooth muscle hypertrophy in the WKY rats. Similarly we observed a reduction in vessel compliance and a reduction in collagen mRNA levels in the SHRSP fed the HK diet . Other studies have also suggested that dietary potassium supplementation improves vessel compliance in patients with essential hypertension . In the current study we did not observe a difference in compliance or vessel stiffness, therefore it is unlikely that this is the mechanism for the protective effect of potassium.
It should be noted that the effects of dietary potassium supplementation on the outcome of cerebral ischemia may not be due solely to the changes in lumen diameter. A small increase in potassium concentration causes a reduction in reactive oxygen species (ROS) generation . ROS generation has also been implicated in the pathogenesis of acute ischemic stroke , therefore a reduction in ROS generation after the induction of ischemia could be responsible for the beneficial effects of potassium on the outcome of ischemia. Similarly, the pro-inflammatory cytokine, interleukin 1 beta (IL-1β) levels increase rapidly in the brain in response to an ischemic insult . Interestingly, we have shown that dietary potassium supplementation in SHRSP causes a dramatic reduction in the plasma concentration of IL-1β , presenting the possibility that this too has an effect on the outcome of ischemia in the normotensive rat.
In conclusion, we have shown very clear evidence that dietary potassium supplementation reduces the amount of damage caused by cerebral ischemia and increases the MCA lumen and outer diameter in WKY rats. To the best of our knowledge this is the first study to assess the effectiveness of this very simple treatment and cost effective treatment in a normotensive rat.
This work was supported by grants from the National Institutes for Health (HL077385: AMD, HL67303:DWS, HL64776:DMP) and the American Heart Association (0030370Z:DWS, 0640113N:DMP, 0130364N:AMD). The authors would like to thank Hiram Ocasio and Meghan Patchan for their technical assistance.
- Ascherio A, Rimm EB, Hernan MA, Giovannucci EL, Kawachi I, Stampfer MJ, Willett WC: Intake of potassium, magnesium, calcium, and fiber and risk of stroke among US men. Circulation 1998,98(12):1198-1204.View ArticleGoogle Scholar
- Fang J, Madhavan S, Alderman MH: Dietary potassium intake and stroke mortality. Stroke 2000,31(7):1532-1537.View ArticleGoogle Scholar
- Suter PM: The effects of potassium, magnesium, calcium, and fiber on risk of stroke. Nutr Rev 1999,57(3):84-88.Google Scholar
- Yamori Y, Nara Y, Mizushima S, Sawamura M, Horie R: Nutritional factors for stroke and major cardiovascular diseases: international epidemiological comparison of dietary prevention. Health Rep 1994,6(1):22-27.Google Scholar
- Tobian L, Lange JM, Ulm KM, Wold LJ, Iwai J: Potassium prevents death from strokes in hypertensive rats without lowering blood pressure. J Hypertens Suppl 1984,2(3):S363-6.Google Scholar
- Tobian L, Lange JM, Johnson MA, MacNeill DA, Wilke TJ, Ulm KM, Wold LJ: High-K diets reduce brain haemorrhage and infarcts, death rate and mesenteric arteriolar hypertrophy in stroke-prone spontaneously hypertensive rats. J Hypertens Suppl 1986,4(5):S205-7.Google Scholar
- Dorrance AM, Osborn HL, Grekin R, Webb RC: Spironolactone reduces cerebral infarct size and EGF-receptor mRNA in stroke-prone rats. Am J Physiol Regul Integr Comp Physiol 2001,281(3):R944-50.Google Scholar
- Dorrance AM, Pollock DM, Romanko OP, Stepp DW: A high-potassium diet reduces infarct size and improves vascular structure in hypertensive rats. Am J Physiol Regul Integr Comp Physiol 2007,292(1):R415-22.View ArticleGoogle Scholar
- Hankey GJ: Potential new risk factors for ischemic stroke: what is their potential? Stroke 2006,37(8):2181-2188. 10.1161/01.STR.0000229883.72010.e4View ArticleGoogle Scholar
- Longa EZ, Weinstein PR, Carlson S, Cummins R: Reversible middle cerebral artery occlusion without craniectomy in rats. Stroke 1989,20(1):84-91.View ArticleGoogle Scholar
- Heagerty AM, Aalkjaer C, Bund SJ, Korsgaard N, Mulvany MJ: Small artery structure in hypertension. Dual processes of remodeling and growth. Hypertension 1993,21(4):391-397.View ArticleGoogle Scholar
- Pollock DM, Pollock JS: Evidence for endothelin involvement in the response to high salt. Am J Physiol Renal Physiol 2001,281(1):F144-50.Google Scholar
- Izzard AS, Graham D, Burnham MP, Heerkens EH, Dominiczak AF, Heagerty AM: Myogenic and structural properties of cerebral arteries from the stroke-prone spontaneously hypertensive rat. Am J Physiol Heart Circ Physiol 2003,285(4):H1489-94.View ArticleGoogle Scholar
- Baumbach GL, Heistad DD: Remodeling of cerebral arterioles in chronic hypertension. Hypertension 1989,13(6 Pt 2):968-972.View ArticleGoogle Scholar
- Wu G, Tian H, Han K, Xi Y, Yao Y, Ma A: Potassium magnesium supplementation for four weeks improves small distal artery compliance and reduces blood pressure in patients with essential hypertension. Clin Exp Hypertens 2006,28(5):489-497. 10.1080/10641960600798705View ArticleGoogle Scholar
- McCabe RD, Bakarich MA, Srivastava K, Young DB: Potassium inhibits free radical formation. Hypertension 1994,24(1):77-82.View ArticleGoogle Scholar
- Juurlink BH, Sweeney MI: Mechanisms that result in damage during and following cerebral ischemia. Neurosci Biobehav Rev 1997,21(2):121-128. 10.1016/S0149-7634(96)00001-2View ArticleGoogle Scholar
- Huang J, Upadhyay UM, Tamargo RJ: Inflammation in stroke and focal cerebral ischemia. Surg Neurol 2006,66(3):232-245. 10.1016/j.surneu.2005.12.028View ArticleGoogle Scholar
- Dorrance AM: Reduced interleukin 1-beta: a possible mechanism for the protective effect of dietary potassium. Hypertension 2004, 44: P112. 10.1161/01.HYP.0000138068.03893.40View ArticleGoogle Scholar
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