NaCl plus chitosan as a dietary salt to prevent the development of hypertension in spontaneously hypertensive rats

Sung-Hoon Park; Noton Kumar Dutta; Min-Won Baek; Dong-Jae Kim; Yi-Rang Na; Seung-Hyeok Seok; Byoung-Hee Lee; Ji-Eun Cho; Geon-Sik Cho; Jae-Hak Park

doi:10.4142/jvs.2009.10.2.141

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Park, Dutta, Baek, Kim, Na, Seok, Lee, Cho, Cho, and Park: NaCl plus chitosan as a dietary salt to prevent the development of hypertension in spontaneously hypertensive rats

Original Article

Journal of Veterinary Science

Journal of Veterinary Science 2009; 10(2): 141-146.

Published online: 11 June 2009

DOI: https://doi.org/10.4142/jvs.2009.10.2.141

NaCl plus chitosan as a dietary salt to prevent the development of hypertension in spontaneously hypertensive rats

Sung-Hoon Park^1,^†, Noton Kumar Dutta^1,^†, Min-Won Baek¹, Dong-Jae Kim¹, Yi-Rang Na¹, Seung-Hyeok Seok¹, Byoung-Hee Lee¹, Ji-Eun Cho², Geon-Sik Cho², Jae-Hak Park¹

¹Laboratory Animal Medicine, and KRF Priority Zoonotic Disease Research Institute, College of Veterinary Medicine, Seoul National University, Seoul 151-742, Korea.

²Biotech , Mokpo 530-370, Korea.

Corresponding author: Tel: +82-2-880-1256; Fax: +82-2-887-1257, pjhak@snu.ac.kr

Equal contributor:

†First two authors contributed equally to this work.

Abstract

The effect of NaCl plus 3% chitosan on the systolic blood pressure of spontaneously hypertensive rats (SHR) were evaluated and compared with NaCl plus KCl (NaCl, 49.36% + KCl 49.36%) and chitosan or NaCl treatment alone. In SHR, administration of NaCl plus chitosan (44 mM Na/day) for two months significantly decreased the systolic blood pressure greater than of NaCl plus KCl and NaCl alone. NaCl plus chitosan resulted, though not statistically significant, in decreased urinary Na⁺ excretion and decreased blood urea nitrogen levels. Urinary creatinine of NaCl plus chitosan was slightly decreased compared to 3 treated groups. Serum electrolytes levels, however, remained unchanged. The combination of NaCl and chitosan may be superior to the conventional use of NaCl plus KCl or NaCl alone in the prevention of hypertension. Even though these supplementary diets have demonstrated potential anti-hypertensive effects in the experimental animal model, further research is needed before any recommendations can be made.

Keywords: chitosan, hypertension, KCl, NaCl, spontaneously hypertensive rat

Introduction

Hypertension is one of the most common cardiovascular diseases and has become a worldwide problem of epidemic proportions, affecting 15-20% of all adults [10,11,22,26]. It is the most serious common chronic health problem because it is a significant risk factor for the development of arteriosclerosis, stroke, myocardial infarction, and end-stage renal disease [25]. Chloride ions (Cl^-) may play a role in the development and severity of age-related hypertension [23]. Therefore, decreasing the dietary intake of sodium chloride (NaCl) is generally recommended [23,25].

Hypertension is explained by the physiological and biochemical reactions of peripheral renin-angiotensin system, and its treatment is focused on the inhibition of angiotensin converting enzyme (ACE) activities for direct inhibition of hypertension. The naturally occurring polysaccharide, antihypertensive, biopolymer chitosan is an ideal candidate for an ACE inhibitor because it is considered to be milder and safer as compared with the drugs commonly used in the treatment of hypertension. In addition, chitosan is usually well-absorbed and demonstrates a multitude of other beneficial physiological properties [8,15].

The naturally occurring biopolymer, chitin-chitosan, is a well-known food supplement that effectively lowers blood cholesterol concentration and controls obesity [19]. In addition, it has many other useful biomedical applications-e.g., an absorbable suture, a drug carrier, an antitumor agent, a hemostatic agent, and a wound-healing agent. Chitosan itself has been developed as a new physiologically bioactive material, which has been touted as a treatment for various disorders, including asthma, atopic dermatitis, arteriosclerosis, hypertension, macular degeneration, arthritis, cancer, diabetes, and osteoporosis, among others [8,14,15].

This study was undertaken to examine the possible effects of chitosan alone and in combination with NaCl in spontaneously hypertensive rat (SHR) models. We also performed a comparative evaluation with the conventional use of NaCl plus KCl in an effort to find a better antihypertensive table salt for people to whom salt-restricted diets are indicated [13,17,18,27].

Materials and Methods

Aqueous chitosan solution

Chitosan was prepared by Biotech (Korea). To produce chitin, crab shells were ground into 180-250 mm particles with a ball mill. The powder was then placed in 2N HCl solution in room temperature for 12 h. Calcium, other inorganic materials, and proteins were then removed with 1 N NaOH to produce chitin. The chitin was then centrifuged and washed with distilled water, ethanol, and ether, in order, and vacuum dried at 70℃ to produce refined chitin in white powder form. It was then hydrolyzed with 50% NaOH solution at 100℃ for 5 h followed by 90% degree of deacetylation to produce chitosan containing 5% water and having a molecular weight of 100,000. A total of 52.5 g of flake-type chitosan was mixed with 950 g of 3% sodium acetate solution using a stirrer and filtered with nylon filter (200 mesh) to acquire a 5% chitosan solution (pH 4.5). A total of 324 g of natural sea salt (NaCl) containing 8% water, measured with a moisture meter (MA30-000v3; Sartorius AG, Germany), was dissolved in 1,000 ml of distilled water, followed by the addition of 180 ml of 5% chitosan solution. The resulting mixture was heated at 90℃ for required concentration by evaporation of water.

Animals and diets

In vivo experiments were performed following the guidelines for the care and use of laboratory animals approved by Seoul National University [Approval No. SNU-070119-1]. Twenty-five SHR, 6 weeks of age and weighing 280-310 g (male) were purchased from Central Laboratory Animal, Korea. Animals were maintained in a certified animal house under supervision and standard conditions of 22 ± 2℃ and 55 ± 10% relative humidity with a photoperiod of 12 : 12 h of light : darkness. Water and a dry pellet diet (Purina Rodent Laboratory Chow; Ralston Purina, USA) were given ad libitum. The rats were acclimatized for 4 days prior to the start of the experiments and randomly allocated to five groups. Group 1: NaCl + KCl (49.36% NaCl plus 49.36% KCl), group 2: NaCl + chitosan (NaCl plus 3% chitosan), group 3: NaCl, group 4: chitosan (3%) administered orally using a metal gastric zonde, and group 5; untreated control. The concentration of sodium given was 44 mM (1 g of sodium) / day [3].

After two months of consuming their respective diets, all rats were anaesthetized by an intramuscular injection of ketamine (100 mg/kg) and xylazine (10 mg/kg) into the right quadriceps femoris muscle. Blood and urine were collected from the heart and urinary bladder, respectively, followed by cervical dislocation.

Body weight and systolic blood pressure

The body weights of the rats were measured once per week at the same time during the day. Measurement of the systolic blood pressure was performed once per week at the same time during the day. After the stabilization of the animals in a warm box at 37℃ for 15 min, the tail systolic blood pressure was measured with a non-invasive blood pressure system (ML125/R; AD Instruments Power Lab System, USA) and was reported as the mean value of three consecutive measurements [28].

Blood and urine chemistry

Blood was centrifuged at 3,000 g for 15 min to obtain serum. After serum separation, we measured the levels of electrolytes [sodium (Na⁺), chlorine (Cl^-) and potassium (K⁺)] by an electrolyte measurement apparatus based on an ion electrode method. Angiotensin I and II were measured with a rat angiotensin I and II EIA kits (Phoenix Pharmaceuticals, USA) according to the manufacturer's instructions.

Urine was assayed for creatinine by a refractometer (Atago, Japan), blood urea nitrogen (BUN) by a commercial kit (BUN Kainos; Kainos, Japan) according to a modified urease-indole-phenol method and electrolytes (Na⁺, Cl^- and K⁺) by an electrolyte measurement apparatus based on an ion electrode method [6].

Histopathology

The autopsied heart and kidneys from five rats in each dietary group of SHR were fixed in 10% formalin buffer for 48 h, followed by dehydration in an alcohol-xylene series prior to embedding in paraffin wax. The glomerular, vascular, tubular, and interstitial changes were graded from 0 to 3 observing H&E stained slides (0 = normal; 0.5 = minimal; 1 = slight; 2 = moderate and 3 = severe) [1].

Statistical data

Statistical analysis was performed using Duncan's multiple range test (Version 8.2; SAS Institute, USA). A p-values < 0.05 were considered statistically significant.

Results

Survival, Body weight and Systolic blood pressure

None of the animals died. All groups had an increase in body weight during the experimental period. At the end of the experiment, the control group gained 74.34 ± 10.91 g from baseline, while the chitosan, chitosan plus NaCl, and KCl plus NaCl treated groups increased by 77.67 ± 8.70 g, 74.16 ±10.40 g, and 61.53 ± 14.70 g, respectively. Throughout the experimental period, no statistically significant difference in body weight changes was observed between all treated groups and control group (Fig. 1). The food intake was essentially proportional to its change in weight (data not shown).

A continuous increase (control: 195.60 ± 7.90 to 215.50 ± 5.20 mmHg) in the systolic blood pressure (SBP) was seen in all the groups during the experimental period. In general, SBP of the NaCl plus chitosan-treated group was lower than that of the KCl plus NaCl-treated group (232.50 ± 7.60 mmHg) and the NaCl-treated group and higher than that of the chitosan-treated group (212.40 ± 5.70 mmHg) and control group. There was a significant decrease (p < 0.05) in SBP in the pure NaCl plus chitosan group at 2 week only when compared to the KCl plus NaCl treated group, but not at 8th week (Fig. 2).

Blood and urine chemistry

Angiotensin I and II concentration, NaCl plus chitosan diet showed 4.71 ± 1.50 ng/ml which was 4.89% higher angiotensin I than control diet (4.49 ± 0.88 ng/ml). KCl plus NaCl diet showed 10.46% less angiotensin I than the control. Angiotensin II of NaCl plus chitosan and KCl plus NaCl was decreased to 2.44% and 0. 85%, respectively, compared to the control group. No consistent differences in final serum angiotensin I and II were seen among the five groups (Fig. 3).

In this study, serum electrolytes were similar and unchanged in all groups (Fig. 4). In general, sodium levels were the highest followed by chlorine and potassium. Na⁺, K⁺ and Cl^- levels in the urine did not differ significantly between the control and the test groups regardless of treatments, but there was a tendency toward an decrease in urinary Na⁺ excretion when treated with NaCl plus chitosan compared to NaCl + KCl or NaCl alone group (Fig. 5).

The NaCl plus chitosan treated group had decreased BUN levels compared to NaCl + KCl or NaCl alone groups, though none of these were statistically significant (p < 0.05).

BUN levels were the lowest (2564.00 ± 454.37 mg/ dl) in the NaCl plus chitosan treated group and highest (3006.00 ± 1236.82 mg/dl) in the control group, followed by the NaCl plus KCl groups (2838.80 ± 858.77 mg/dl) (Fig. 6A).

Levels of urinary creatinine (Fig. 6B) significantly decreased in all four treated groups compared to the control (133.96 ± 51.37 mg/dl). The creatinine was lowest in the NaCl plus chitosan group (80.06 ± 22.98 mg/dl); therefore, the proximal tubules were thought to be less disturbed in the rats exposed to daily levels of NaCl plus chitosan over a period of 8 weeks.

Levels of urinary creatinine (Fig. 6B) significantly decreased in all four treated groups compared to the control (133.96 ± 51.37 mg/dl) (p < 0.05). The creatinine was lowest in the NaCl plus chitosan group (80.06 ± 22.98 mg/ dl); therefore, the proximal tubules were thought to be less disturbed in the rats exposed to daily levels of NaCl plus chitosan over a period of 8 weeks.

Histopathological findings

As expected, SHR of all experimental groups were hypertensive, but there were no histopathological signs in tissue properties (data not shown).

Discussion

Hypertension is a major risk factor for cardiovascular diseases such as heart failure, stroke, coronary artery disease, and myocardial infarction [12]. It is called the 'silent killer' for good reason: Almost one-third of individuals with hypertension do not know that they have it and almost 50% of those who do know they have hypertension do not control it properly. Hypertension is the primary or a contributing cause of death in over 200,000 patients per year in the United States alone [20]. Therefore, there is an urgent need for significant research to develop new medicine to treat hypertension. There are a great number of pharmaceuticals that have been proven to be effective in lowering blood pressure, but usually have side effects [5]. Diet and lifestyle modification may also be effective tools for the prevention of hypertension, which could decrease the need for antihypertensive drugs [2].

The link between sodium intake and hypertension remains controversial due to inconsistencies between early epidemiologic studies, which showed a strong positive relationship between salt intake, blood pressure, and the incidence of hypertension, and more recent studies, which showed only modest decreases in blood pressure with sodium reduction, particularly in the normotensive population [3]. Chrysant et al. [3] reported an increased risk of heart attacks and cardiovascular mortality in persons who appeared to have restricted their sodium intake, suggesting that sodium reduction may be harmful under some circumstances. In this respect, the search for diet- related preventive measures against hypertension is obviously of interest and within the scope of functional foods.

In the present study, we compared the consumption of an effective amount of NaCl plus KCl, NaCl, NaCl plus chitosan, and chitosan by SHRs in an effort to find a suitable agent for salting food that has saltiness of NaCl, but with antihypertensive effects. We were particularly interested in the SHR rats because they represent an animal model of the genetic predisposition to develop arterial hypertension during aging, and they have numerous similarities to humans with essential hypertension [2,21].

This study showed that body weight increased progressively with aging and in all groups to a similar extent. The control SHR gained more weight than the other groups, and after week 8, the body weight tended to be lower in the NaCl plus chitosan group than that in the chitosan alone group, but not to a significant extent. NaCl plus 3% chitosan tended to reduce the blood pressure in SHRs with greater efficacy than NaCl plus KCl and NaCl alone.

Urinary electrolyte concentrations of Cl^- increased only when KCl was supplemented with NaCl and the level of Na⁺, K⁺ and Cl^- was lower when SHRs were treated with NaCl plus chitosan compared to NaCl alone. The serum electrolyte concentrations of Na⁺ and K⁺ were identical across all groups. On the other hand, the BUN levels of the NaCl plus chitosan-treated groups were lower than that of the control group. This finding on the BUN level suggested a decrease in glomerular filtration which may be explained by the decrease of blood pressure due to the increase of angiotensin I or the decrease of angiotensin II production [7,9,16,24]. Since urea is a final product in protein metabolism and is excreted in the urine via the kidney, the BUN level is important in the evaluation of renal function. Although urinary creatinine unexpectedly increased in control group, it was the lowest in the NaCl plus chitosan group. This finding indicates that the anti-hypertensive effect of NaCl plus chitosan may be due to the amelioration of kidney function in the experimental animal models. This combination may be a better option for dietary supplementation than the conventional uses of NaCl plus KCl or NaCl alone.

This study concluded that the consumption of NaCl plus chitosan - based functional dietary salt should be encouraged as part of an overall lifestyle medicine approach for the prevention of hypertension. To our knowledge, this is the first report showing the antihypertensive effect of a composition of NaCl plus chitosan. This composition may be applied as a substitute table salt for imparting saltiness to dishes or as an ingredient in crackers, snack foods, and other food products requiring salt, which would be particularly appropriate for patients recommended to decrease the amount of salt in their diet. As there are several limitations in this study, further research is needed to identify bioactive compound(s) and the anti-hypertensive mechanism(s) of action of NaCl plus chitosan.

Figures and Tables

Fig. 1

Changes in body weight of spontaneously hypertensive rats administered dietary salts over the experimental period. Vertical bars represent the mean ± SD (n = 5).

Fig. 2

Changes in systolic blood pressure of spontaneously hypertensive rats administered various combinations of dietary salts. Means with the same alphabetical letter are not significantly different (p < 0.05). Vertical bars represent the mean ± SD (n = 5).

Fig. 3

Effect of dietary salts on serum angiotensin 1 and 2 concentrations (3A and 3B). Vertical bars represent the mean ± SD (n = 5).

Fig. 4

Effect of dietary salts on serum electrolytes (Na⁺, K⁺ and Cl^-). Vertical bars represent the mean ± SD (n = 5).

Fig. 5

Effect of dietary salts on urine electrolytes (Na⁺, K⁺ and Cl^-). Vertical bars represent the mean ± SD (n = 5).

Fig. 6

Influence of different diets on urine blood urea nitrogen and creatinine levels in spontaneously hypertensive rats. Means with the different alphabetical letter are significantly different (p < 0.05) compared with the control group.

Acknowledgments

This work was supported by grants provided by the Korea Research Foundation (KRF-2006-J02901) and BK 21 project, Korea. Dr. N. K. Dutta was supported by a fellowship from the Korea Research Foundation.

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