Nitric oxide synthase blockade and body fluid volumes

Braz J Med Biol Res, January 2002, Volume 35(1) 131-134 (Short Communication)

Nitric oxide synthase blockade and body fluid volumes

A.M. Balaszczuk^1,2,3, A. Tomat¹,S. Bellucci¹, A. Fellet¹ and C. Arranz^1,2,3

¹Departamento de Fisiología, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Buenos Aires, Argentina

²Fundación Barceló, Buenos Aires, Argentina

³IQUIMEFA-PROSIVAD CONICET, Buenos Aires, Argentina

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References

^{Correspondence and Footnotes}

Abstract

The influence of chronic nitric oxide synthase inhibition with N^G-nitro-L-arginine methyl ester (L-NAME) on body fluid distribution was studied in male Wistar rats weighing 260-340 g. Extracellular, interstitial and intracellular spaces, as well as plasma volume were measured after a three-week treatment with L-NAME (»70 mg/kg per 24 h in drinking water). An increase in extracellular space (16.1 ± 1.1 vs 13.7 ± 0.6 ml/100 g in control group, N = 12, P<0.01), interstitial space (14.0 ± 0.9 vs 9.7 ± 0.6 ml/100 g in control group, P<0.001) and total water (68.7 ± 3.9 vs 59.0 ± 2.9 ml/100 g, P<0.001) was observed in the L-NAME group (N = 8). Plasma volume was lower in L-NAME-treated rats (2.8 ± 0.2 ml/100 g) than in the control group (3.6 ± 0.1 ml/100 g, P<0.001). Blood volume was also lower in L-NAME-treated rats (5.2 ± 0.3 ml/100 g) than in the control group (7.2 ± 0.3 ml/100 g, P<0.001). The increase in total ratio of kidney wet weight to body weight in the L-NAME group (903 ± 31 vs 773 ± 45 mg/100 g in control group, P<0.01) but not in total kidney water suggests that this experimental hypertension occurs with an increase in renal mass. The fact that the heart weight to body weight ratio and the total heart water remained constant indicates that, despite the presence of high blood pressure, no modification in cardiac mass occurred. These data show that L-NAME-induced hypertension causes alterations in body fluid distribution and in renal mass.

Key words: Nitric oxide, Kidney, Heart, Body fluid, Hypertension, Extracellular space, Intracellular space, L-NAME

Nitric oxide (NO) has an important role in the physiologic control of blood pressure. Alterations in NO synthesis may be involved in the pathogenesis of hypertension. There is evidence that the short-term and long-term in vivo administration of nitric oxide synthase (NOS) inhibitors such as N^G-nitro-L-arginine methyl ester (L-NAME) induces a dose- and time-dependent increase in arterial blood pressure in conscious rats and adaptive changes in the functions of the kidney, heart and vessels (1). Three NOS isoforms (neuronal, inducible and endothelial) are expressed in the heart in a cell-specific manner (2) and in rat kidney, but it is unclear which NOS isoform(s) is/are responsible for the functional effects (3). The response to chronic NOS inhibition is likely to depend upon several factors, including the cellular source of NO, the amount released, the target tissue and interactions with neurohumoral factors (4). Recent investigations have shown that the chronic model of hypertension with L-NAME is generally associated with an architectural modification of cardiovascular tissues as well as with tubular and renal hemodynamic changes (1,5). Moreover, it is likely that the modifications of renal and cardiovascular functions induced with L-NAME could lead to an abnormal control of body fluid volume (6). However, little information is available about the effect of chronic NOS inhibition on body volumes. On the basis of these considerations, we have studied the effect of chronic blockade of NO synthesis with L-NAME on body fluid distribution and on renal and cardiac tissue.

Long-term L-NAME treatment was performed on male Wistar rats weighing 260-340 g, obtained from Facultad de Farmacia y Bioquímica breeding laboratories (Universidad de Buenos Aires, Argentina). Animals were housed in a temperature- and humidity-controlled environment with automatic lighting in 12-h cycles and maintained on standard rat chow (Nutrimentos Purina, Buenos Aires, Argentina) and tap water ad libitum up to the day of the experiments. Animals were used in compliance with the Research Animals Use Guideline of the American Heart Association. A group of eight rats received L-NAME (Sigma, St. Louis, MO, USA) in the drinking water for three weeks, while 12 age-matched control rats received drinking tap water alone. The concentration of L-NAME was adjusted according to body weight and water intake, resulting in a daily intake of approximately 70 mg/kg. At the end of treatment, systolic blood pressure was measured by the tail-cuff method using a Grass polygraph (model 79H, Grass Instruments Co., Quincy, MA, USA). All rats were anesthetized with urethane (Sigma), 1 g/kgbody weight, ip. Under aseptic conditions, both kidneys were removed through bilateral lumbar incisions. After performing a tracheotomy, the right jugular vein and the left carotid artery were catheterized for drug administration and later recovery of blood.

The extracellular space was determined as inulin space by injecting 0.7 ml of a 13% inulin solution into the jugular vein, and an enzymatic method was used for the determination of plasma inulin (7). Plasma volume was evaluated according to the method of Wang (8) using Evans blue as indicator. The intracellular space was determined as the difference between total water and extracellular space. The interstitial space was obtained by subtracting plasma volume from inulin space. Total water was estimated as the difference between rat wet weight and dry weight. Dry weight was obtained by placing the dead rats and their organs in an oven at 100ºC for three days (9). The hematocrit was measured by spinning in a microfuge the blood collected into microhematocrit tubes. Plasma albumin concentration was determined by a colorimetric method (bromocresol phthalein, Wienner Laboratories, Rosario, Argentina). Statistical differences between groups were evaluated by the Student t-test and a 5% probability level was used as a criterion for significance. Values are reported as means ± SEM. The Prism software (Graph Pad Software) was used for statistical analysis.

Systolic blood pressure was significantly higher in animals after three weeks of L-NAME treatment compared with control rats (161 ± 7 vs 113 ± 3 mmHg, P<0.001). Body weight of control rats was similar to that of the L-NAME group (267 ± 8 and 273 ± 9 g, respectively). Furthermore, L-NAME treatment induced a significant increase in extracellular space, interstitial space and total water compared with control rats (Table 1). Plasma volume and blood volume were significantly lower in the L-NAME group, whereas no significant changes occurred in the hematocrit values (control: 51 ± 1, L-NAME: 49 ± 3%). There was no significant difference in intracellular space between the control and L-NAME groups. The relationship between plasma volume and interstitial space decreased significantly in the L-NAME group compared with control rats (0.21 ± 0.02 to 0.40 ± 0.04, respectively, P<0.001). Plasma albumin concentration did not change significantly after L-NAME administration (control: 2.25 ± 0.12, L-NAME: 1.90 ± 0.14 g/100 ml).

 

The kidney weights of control and L-NAME-treated groups are listed in Table 2. The total ratio of kidney wet weight to body weight showed a significant increase after treatment with L-NAME, and the kidney water/wet kidney ratio remained unchanged.

 

Finally, no effects on cardiac mass were observed after L-NAME treatment (L-NAME: 347 ± 11, control: 362 ± 7 mg/100 g) or on heart water/wet heart ratio (L-NAME: 79.1 ± 0.4, control: 76.7 ± 1.4 ml/100 g).

The increase in extracellular space with the decrease in plasma volume observed in our experimental model indicates an increase of interstitial tissue compliance that permits the accumulation of fluids in this compartment. The increase in extracellular space, like total water, may be associated with a progressive antidiuretic and antinatriuretic effect induced by L-NAME administration, which can be only partially offset by the increase in blood pressure, promoting pressure natriuresis mechanisms (10,11).

These body fluid changes in animals submitted to chronic L-NAME administration suggest that the hypertension observed could be, at least in part, volume dependent. In addition to the increase in vascular reactivity induced by NOS blocking, the extracellular fluid volume increase may provoke an increase of cardiac output which, after a variable period of time, may induce an increase in peripheral resistance by an autoregulation mechanism (12). However, the effects of L-NAME administration on cardiac output remain unclear, and the different results reported in the literature may be due to differences in the experimental designs (10,13,14).

Furthermore, we observed that chronic administration of L-NAME caused a slight nonsignificant decrease in plasma albumin. This result agrees with published findings demonstrating that chronic NOS inhibition causes accelerated proteinuria, leading to a plasma protein decrease (6,11). This may result in an increase in the interstitial space probably due to fluid efflux from the plasma space. We have also observed that the plasma volume contraction did not cause a significant change in hematocrit; probably the amount of volume involved was too small to cause any alteration of this parameter. The changes in body volumes induced by L-NAME administration were not reflected in body weight.

On the other hand, the total ratio of kidney wet weight to body weight increased significantly after L-NAME treatment, whereas the kidney water/wet kidney weight ratio remained constant, indicating an increase of renal mass. Numerous studies have demonstrated that chronic NOS inhibition in experimental models and in humans may produce deleterious effects on renal tissues and function, leading to abnormalities in renal response (11,15,16), whereas others have found an increase in protein synthesis in the kidney (17). These findings could explain, at least in part, the hypertrophy observed in our experimental model.

It was reported that chronic L-NAME treatment causes cardiovascular metabolic alterations and myocardial remodeling (18). These changes would be expected to induce cardiac hypertrophy as a compensatory response that depends on the duration and magnitude of the rise in blood pressure. However, in our experimental design the chronic L-NAME treatment induced hypertension without changes in cardiac mass, in agreement with other studies, supporting the hypothesis that the adaptation to pressure overload may occur without changes in cardiac mass (19).

The results of the present study suggest that the chronic rise in arterial blood pressure induced by long-term blockade of NO synthesis involves an abnormal body fluid distribution in addition to the increase in vascular reactivity already described. The increase in renal mass could be a consequence of NO pathway inhibition and/or the activation of other systems in response to the altered electrolyte and water metabolism.

Address for correspondence: A.M. Balaszczuk, Junín 956, Piso 7, 1113 Buenos Aires, Argentina. Fax: [phone]. E-mail: [e-mail]

Research supported by Universidad de Buenos Aires, Fundación Barceló and IQUIMEFA-PROSIVAD CONICET, Buenos Aires, Argentina. Received June 11, 2001. Accepted October 10, 2001.

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Correspondence and Footnotes

Publication Dates

• Publication in this collection
  07 Dec 2001
• Date of issue
  Jan 2002

History

• Received
  11 June 2001
• Accepted
  10 Oct 2001