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Chronic intermittent hypercapnic hypoxia increases pulmonary arterial pressure and haematocrit in rats

Dept of Physiology, Royal College of Surgeons in Ireland, St. Stephen's Green, Dublin, Ireland

CORRESPONDENCE: A. Bradford, Dept of Physiology, Royal College of Surgeons in Ireland, St. Stephen's Green, Dublin 2, Ireland. Fax: 353 014022447

Keywords: haematocrit, hypercapnia, hypoxia, pulmonary arterial pressure, sleep apnoea

Received: September 9, 2000
Accepted March 26, 2001

	Abstract

TOP Abstract Materials and methods Results Discussion Acknowledgements References

 
Sleep-disordered breathing is associated with pulmonary hypertension and raised haematocrit. The multiple episodes of apnoea in this condition cause chronic intermittent hypoxia and hypercapnia but the effects of such blood gas changes on pulmonary pressure or haematocrit are unknown. The present investigation tests the hypothesis that chronic intermittent hypercapnic hypoxia causes increased pulmonary arterial pressure and erythropoiesis.

Rats were treated with alternating periods of normoxia and hypercapnic hypoxia every 30 s for 8 h per day for 5 days per week for 5 weeks, as a model of the intermittent blood gas changes which occur in sleep-disordered breathing in humans. Haematocrit, red blood cell count and haemoglobin concentration were measured each week and systemic and pulmonary arterial blood pressure and heart weight were measured after 5 weeks.

In relation to control, chronic intermittent hypercapnic hypoxia caused a significant increase in systemic (104.3±4.7 mmHg versus 121.0±10.4 mmHg) and pulmonary arterial pressure (20.7±6.8 mmHg versus 31.3±7.2 mmHg), right ventricular weight (expressed as ratios) and haematocrit (45.2±1.0% versus 51.5±1.5%).

It is concluded that the pulmonary hypertension and elevated haematocrit associated with sleep-disordered breathing is caused by chronic intermittent hypercapnic hypoxia.

Sleep disordered breathing affects 1–4% of adults 1. It is associated with multiple episodes of hypoxia and hypercapnia due to hypopnoea or apnoea, which are either caused by intermittent collapse of the upper airway (UA), termed obstructive sleep apnoea (OSA; the most common form of sleep disordered breathing), or a reduced drive to breath, termed central apnoea 2. The condition is associated with a number of cardiovascular changes, including increased pulmonary and systemic arterial blood pressure, right ventricular hypertrophy, cardiac arrhythmias and increased haematocrit. Diurnal pulmonary hypertension is present in 17–42% of OSA patients 3–7 and represents a serious threat to long-term outcome in these patients 8. The cause of pulmonary hypertension in these patients is unknown. During an apnoeic event, pulmonary arterial pressure is acutely increased 9, presumably due to hypoxic pulmonary vasoconstriction, so that repetitive episodes of increased pressure may ultimately give rise to daytime pulmonary hypertension 10. In support of this, it has recently been shown that chronic intermittent hypocapnic hypoxia in rats causes right ventricular hypertrophy, suggesting that pulmonary arterial pressure is increased 11. However, apnoeas are accompanied by hypercapnia as well as hypoxia 12, but the effects of this combination of chronic intermittent blood gas changes on pulmonary arterial pressure are unknown. It is known that chronic continuous hypercapnia protects against the effects of continuous hypoxia on right ventricular weight and pulmonary arterial pressure 13. Therefore, it is not clear whether prolonged intermittent hypercapnia in association with prolonged intermittent hypoxia would affect right ventricular weight or pulmonary arterial pressure. However, in view of the association of pulmonary hypertension with OSA, the present investigation tests the hypothesis that chronic intermittent hypercapnic hypoxia causes right ventricular hypertrophy and pulmonary hypertension.

Another contributor to increased pulmonary arterial pressure is a raised haematocrit. It has previously been shown that chronic intermittent hypocapnic hypoxia increases the haematocrit in rats 11. A combination of chronic continuous hypoxia and hypercapnia greatly reduces the increase in haematocrit caused by chronic continuous hypoxia alone 13, but the effects of chronic intermittent hypoxia and hypercapnia on haematocrit have not been studied. As with pulmonary hypertension, the presence of increased haematocrit is variable in OSA patients. It has been suggested that an increased haematocrit only occurs in the presence of daytime hypoxaemia 4. Hoffstein et al. 14 reported no change or slight elevations in haematocrit in a large group of sleep apnoea patients without daytime hypoxaemia, whereas Laks et al. 5 did observe an elevated haematocrit in the absence of daytime hypoxaemia. Therefore, in the present investigation, the effects of chronic intermittent hypercapnic hypoxia on haematocrit, right ventricular weight and pulmonary arterial pressure are examined using a rat model which mimics the nocturnal pattern of hypercapnic hypoxia of sleep-disordered breathing in humans.

	Materials and methods

TOP Abstract Materials and methods Results Discussion Acknowledgements References

 
Male Wistar rats (3 months old) were used in this study. Except during the treatment and experimental periods, the rats were housed, four to a cage, under a 12:12 h (light:dark) photoperiod and were given unrestricted access to food and water.

Chronic intermittent hypercapnic hypoxia treatment
Animals were placed in restrainers with their heads surrounded by hoods. Using timed solenoid valves, a mixture of nitrogen (N₂) and carbon dioxide (CO₂) was distributed into the hoods for 15 s at a flow that reduced the ambient fractional inspiratory concentration of oxygen (F_I,O2) to 6–8% and increased the ambient fractional inspiratory concentration of CO₂ (F_I,CO2) to 10–14%. This was followed by an infusion of air for 15 s allowing the F_I,O2 and the F_I,CO2 to return to nominal. This cycle was repeated twice per min, 8 h per day, for 5 days per week for 5 weeks. The control rats were given air for 15 s followed by air for 15 s at the same flow rates as the hypercapnic hypoxia rats. This cycle was repeated twice per min, 8 h per day, 5 days per week for 5 weeks. In all, 16 control and 13 hypercapnic hypoxia rats were treated in this way.

The ambient F_I,O2 and F_I,CO2 in the hoods were measured daily by placing the probes of the O₂ analyser (Engström Eliza Duo, Gambro-Engström AB, Bromma, Sweden) and CO₂ analyser (Capstar-100 end-tidal CO₂ analyzer, CWE Inc., Ardmore, PA, USA) as close as possible to the nose of the hypercapnic hypoxic rats for 5 min at 0, 4 and 8 h throughout the treatment period. These values at 0, 4 and 8 h were averaged for each day (fig. 1). The haematocrit, red blood cell count and haemoglobin concentration were measured on day 0, 7, 14, 21, 28 and 35 of the 5-week treatment period using blood collected from the rat tail artery in microcapillary tubes.

View larger version (31K): [in this window] [in a new window]   Fig. 1.— Values (measured over 5 min) for a) minimum fractional inspiratory concentration of O2 (FI,O2) and b) maximum fractional inspiratory concentration of CO2 (FI,CO2) measured three times per day in eight animals. Values are presented as mean±sd.

Measurement of arterial blood oxygen tension and end-tidal carbon dioxide tension
Untreated rats were used to measure systemic arterial oxygen tension (P_a,O2) and end-tidal carbon dioxide tension (P_ET,CO2) during normoxia/hypercapnic hypoxia treatment. Rats were anaesthetized intraperitoneally (i.p.) with 40 mg·kg^–1 of pentobarbitone (Sagatal, Rhône Mérieux Ltd, Essex, UK). A femoral artery and vein were cannulated and the incision was sutured closed. The cannulae were connected to a three-way tap which housed an O₂ needle electrode. A small ventral midline incision was made in the neck and a small hole was made in the trachea by using a hot needle. A cannula was inserted into the trachea through this hole. The hole was then sealed using nontoxic glue and the cannula was secured. The cannula was attached to a CO₂ end-tidal analyser (Capstar-100 end-tidal CO₂ analyzer, CWE Inc., Ardmore, PA, USA) with a response time of 0.33 s. The rats were allowed to recover and were placed into the treatment chambers to begin the intermittent hypercapnic hypoxia treatment. Heparin (1,000 U·kg^–1, i.v.) was given to ensure that blood flowed without clotting. Alternating periods of air for 15 s and hypercapnic hypoxia treatment (N₂ and CO₂) for 15 s were begun twice per min. P_a,O2 and P_ET,CO2 were continuously measured and F_I,O2 and F_I,CO2 in the hoods were also monitored. All signals were fed to a data acquisition system and recorded on a computer.

Measurement of systemic and pulmonary arterial blood pressure and heart weight
After the 5-week treatment, rats were anaesthetized with pentobarbitone (60 mg·kg^–1, i.p.). The carotid artery was exposed and cannulated, and the blood pressure was measured by attachment of a suitably calibrated pressure transducer. A tracheal cannula was inserted. The pulmonary arterial pressure was measured using the isolated-perfused lung technique 13, 15. This technique has certain advantages over in vivo measurement, in that it is technically easier to use and yields results which are independent of cardiovascular and respiratory changes or reflex effects. Heparin (1 U·g^–1) was injected through the carotid artery cannula. The chest wall was opened and the pulmonary artery was cannulated. The lungs were carefully removed and the tracheal cannula was connected to a small animal ventilator. The pulmonary artery cannula was perfused at constant flow (0.02 mL·g^–1·min^–1) with physiological saline solution containing 2% Dextran, and pulmonary artery pressure was measured from a side-arm of the pulmonary artery cannula using a pressure transducer. The ventilator inflated and deflated the lungs with 5% CO₂ in air at a rate of 50 breaths min^–1 and a volume of 2.5 mL.

The heart was removed and was placed in a 4% formalin solution for 3 days. After this time, the heart was removed from the formalin and the atria were trimmed away and discarded. The right ventricle was separated from the left ventricle and septum and these two portions were weighed separately. The right ventricular weight was expressed as a ratio of the left ventricular weight and also as a ratio of body weight.

Data analysis
Values for body weight, right and left ventricular weight, haematocrit, red blood cell count, haemoglobin concentration, pulmonary arterial pressure, systemic arterial pressure and heart rate were expressed as mean±sd and used to statistically compare the control, hypocapnic hypoxia and hypercapnic hypoxia groups using analysis of variance (ANOVA) and Fischer's least significant difference test, with p<0.05 taken as significant.

	Results

TOP Abstract Materials and methods Results Discussion Acknowledgements References

 
In eight control and six hypercapnic hypoxia-treated rats, the food and water intake were measured over the 5-week treatment period. The control rats ingested 80.5±8.9 g·kg^–1·day^–1 of food and 90.2±8.1 mL·kg^–1·day^–1, of water. These values were similar to those of the hypercapnic hypoxia-treated rats (78.3±11.4 g·kg^–1·day^–1 and 91.3±7.7 mL·kg^–1·day^–1, food and water, respectively). The body weight of the control and hypercapnic hypoxia-treated rats at the beginning of the 5-week treatment period was 343.7±28.5 g and 348.6±35.9 g respectively. The final body weights after 35 days are shown in table 1. The weight change in the control group was +6.3±4.0% (n=16) and in the hypercapnic hypoxia group was –5.6±4.6% (n=13). These differences were statistically significant.

View larger version (17K): [in this window] [in a new window]   Fig. 2.— Recordings of a+b) inspiratory oxygen tension (PI,O2) c+d) arterial oxygen tension (Pa,O2) and e+f) end-tidal carbon dioxide tension (PET,CO2) while breathing air (a,c,e), and alternating periods of normoxia and hypercapnic hypoxia (b, d, f). All recordings are extracts of a continuous record.

View larger version (21K): [in this window] [in a new window]   Fig. 3.— Effects of chronic intermittent hypercapnic hypoxia on a) blood haematocrit; b) red cell count; and c) haemoglobin concentration of control (, n=16) and hypercapnic hypoxia (, n=13) rats during the 5-week treatment period. Values are presented as mean±sd. ***: significantly different (p<0.001) from control using analysis of variance.

Table 1 shows the right ventricular weight expressed as a ratio to the left ventricular weight and to body weight, left ventricular weight as a ratio to body weight and total heart weight as a ratio to body weight. The left ventricular to body weight ratio was unaffected, but the right ventricular to left ventricular weight and right ventricular to body weight ratios were significantly increased in response to chronic intermittent hypercapnic hypoxia, indicating right ventricular hypertrophy.

In a separate group of hypocapnic hypoxia rats (n=8), there was also a significant increase in pulmonary arterial pressure (39.1±18.5 mmHg) compared to controls (n=8, 22.7±7.9 mmHg).

	Discussion

TOP Abstract Materials and methods Results Discussion Acknowledgements References

 
In the present investigation, a rat model of the intermittent blood gas changes associated with sleep-disordered breathing in humans showed that chronic intermittent hypercapnic hypoxia causes systemic arterial and pulmonary hypertension, increased haematocrit and right ventricular hypertrophy. The fall in P_a,O2 to 55 mmHg and the increase in arterial carbon dioxide tension (P_a,CO2) to 60 mmHg during the hypercapnic hypoxia episodes were similar to the values recorded by Fletcher et al. 16 in rats exposed to repetitive episodes of hypercapnic hypoxia twice per min, 6–8 h per day for 35 consecutive days.

One major difference between the present model and patients with OSA is that during the obstructed breaths, marked negative intrathoracic pressures are generated 2. This causes acute haemodynamic changes which may also result in chronic cardiovascular changes 9. Conversely, this model can be viewed as having an advantage that it allows the study of the effects of chronic blood gas changes independently of these mechanical changes. However, the model cannot mimic all of the blood gas changes which occur in OSA. These changes are complex, so that hypoxia can be accompanied by either normocapnia or hypercapnia during the apnoeas and hypocapnia following the apnoeas 12. The body weights of the control and hypercapnic hypoxic rats at the end of the 5-week treatment were not significantly different. However, the actual weight gain of the hypercapnic hypoxic rats was impaired compared to the control rats, despite having ingested similar amounts of food and water. Chronic continuous hypoxia has been shown to impair normal weight gain in rats 17. Whereas chronic continuous hypoxia alone and continuous hypercapnia alone impair weight gain, a combination of continuous hypoxia and hypercapnia causes weight loss 13. For chronic intermittent hypercapnic hypoxia, Fletcher et al. 16 showed that the body weights of the treated rats at the end of 5 weeks were not significantly different from controls, but the actual weight gain was somewhat impaired.

The mean arterial blood pressure was 16% higher in the hypercapnic hypoxia group compared to controls. This hypertensive effect of chronic intermittent hypoxia and hypercapnia has been well described previously 16, 18–22 and its importance stems from the clear association of OSA and systemic hypertension 23–25. Systemic hypertension in the present study was not associated with left ventricular hypertrophy. Although Fletcher and coworkers 16, 18–22 usually observed left ventricular hypertrophy, in one study they found that chronic intermittent hypocapnic hypoxia had no effect on left ventricular weight, despite increased systemic blood pressure 19. In another study, sympathetic-denervated rats exposed to intermittent hypoxia showed an increase in left ventricular weight without an increase in systemic blood pressure 21. This suggests that systemic hypertension may not cause left ventricular hypertrophy but that it is an effect of the intermittent hypoxia itself. Fletcher and coworkers 20–22 have frequently observed hypertrophy of the chambers of the heart in response to chronic intermittent hypoxia without an increase in systemic blood pressure (when this was prevented by sympathectomy or carotid body denervation) and these workers have proposed that it is due to a direct effect of hypoxia. Further evidence for this stems from humans with an anomalous coronary arterial supply from the pulmonary artery 26. In this condition, there is left ventricular hypertrophy but there is no increase in afterload, suggesting that the hypertrophy is due to the supply of hypoxic blood to the ventricle from the pulmonary artery.

The association of pulmonary hypertension and OSA is controversial with 17–42% of OSA patients showing the presence of diurnal pulmonary hypertension 3–7. Right ventricular weight is linearly related to pulmonary arterial pressure in rats and thus right ventricular hypertrophy is an index of pulmonary hypertension 27. Right ventricular weight is increased in rats exposed to continuous hypoxia 27, 2 h of hypoxia per day for 42 days 28 and 30 min of hypoxia per h, 8 h per day for 28 days 29. However, none of these patterns of hypoxia resembles that of OSA. Using a rat model which does mimic the intermittent hypoxia of OSA, Fletcher and coworkers 16, 18, 20, 21 found no change in right ventricular weight. However, in one study using Sprague-Dawley rats, these workers did show that chronic intermittent hypoxia resulted in right ventricular hypertrophy 22 and an unequivocal increase in right ventricular weight has previously been shown, using a similar model 11. The present study shows that chronic intermittent hypercapnic hypoxia also results in an increased right ventricular weight, indicative of raised pulmonary arterial pressure. The effects of chronic intermittent hypoxia or hypercapnic hypoxia on pulmonary arterial pressure have not been previously investigated. It is well known that chronic continuous hypoxia has a significant effect on pulmonary arterial pressure and pulmonary vascular remodelling in animals 13, 27. However, Ooi et al. 13 have shown that hypercapnia combined with hypoxia markedly reduced the pulmonary hypertension and right ventricular hypertrophy observed in rats after chronic continuous hypoxia alone, and inhibited to some degree the pulmonary vascular remodelling that is associated with continuous hypoxia alone. It is thought that this effect of continuous hypercapnia might also occur in intermittent hypercapnic hypoxia and might therefore prevent an increase in pulmonary arterial pressure. Such a mechanism could then explain the absence of pulmonary hypertension in many patients with OSA. However, consistent with the finding of right ventricular hypertrophy, the present results show that chronic intermittent hypocapnic hypoxia and hypercapnic hypoxia cause pulmonary arterial hypertension. The importance of this stems from the suggestion that pulmonary hypertension does not develop in OSA unless it is accompanied by daytime hypoxaemia 3, 30. However, pulmonary hypertension has been observed in some OSA patients without daytime hypoxaemia (P_a,O2 >80 mmHg) 5 or with only slight hypoxaemia (72 mmHg) 31 and the present results support the idea that nocturnal episodic hypercapnic hypoxia causes pulmonary hypertension in the absence of continuous hypoxia 32.

There is considerable controversy concerning the causes of increased haematocrit in OSA. Hoffstein et al. 14 suggested that the intermittent nocturnal hypoxaemia of OSA patients did not lead to polycythaemia, although they did report slight elevations in their haematocrit values. Bradley et al. 3 showed raised haematocrit and pulmonary hypertension in OSA patients, but these also presented daytime hypoxaemia. Goldman et al. 33 showed, in eight OSA patients, that there was no increase in haematocrit despite episodes of profound nocturnal hypoxaemia. Chaouat et al. 4 showed that OSA patients with pulmonary hypertension also had raised haematocrit. This suggested that the causes for pulmonary hypertension were similar to those for raised haematocrit, namely the presence of daytime hypoxaemia 4, 7. However, there are some OSA patients who present both pulmonary hypertension and raised haematocrit without daytime hypoxaemia 5. It may be that in some cases, the intermittent nature of the hypoxia gives insufficient time to stimulate red blood cell production. Alternatively, since concomitant chronic continuous hypercapnia has been shown to greatly reduce the extent of the haematocrit increase caused by chronic hypoxia alone 13, it may be that the intermittent hypercapnia accompanying intermittent hypoxia diminishes the erythropoietic response. In the present investigation, chronic intermittent hypercapnic hypoxia caused a clear increase in haematocrit, which was apparent when first measured at day 7, and persisted for the duration of the treatment period. This shows that concomitant hypercapnia does not prevent the erythropoietic response to intermittent hypoxia.

The increase in haematocrit was apparent at day 7 of the hypercapnic hypoxia treatment. Chronic continuous hypoxia also increases haematocrit within this time period 13 and it has previously been shown that chronic intermittent hypocapnic hypoxia also increases haematocrit when measured at day 7 11. However, it is possible that the rapidity of this response may involve a change in plasma volume. Thus, a decrease in plasma volume without any change in erythropoiesis could cause an increase in haematocrit. However, the effects of hypoxia on plasma volume are highly controversial. In humans, for example, hypoxia has been reported to cause diuresis and natriuresis 34 or to cause antidiuresis and antinatriuresis 35. Similarly, in rats, diuresis and natriuresis 36 or antidiuresis and antinatriuresis 37 have been described. However, more recent evidence suggests that acute hypoxia in rats causes antidiuresis and antinatriuresis 38, 39 and that chronic hypoxia results in normal renal function 40. Therefore, it is believed that a decrease in plasma volume is an unlikely contributor to the increased haematocrit in the present experiments.

The present data show that exposure to chronic intermittent hypercapnic hypoxia induces a number of responses including erythropoiesis, right ventricular hypertrophy and pulmonary and systemic hypertension. These effects are probably due to altered patterns of gene expression and a major activator of the transcription of these genes is hypoxia-inducible factor 1 41. Thus, hypoxia-inducible factor 1 has been shown to participate in the pulmonary and systemic hypertensive, erythropoietic and right ventricular hypertrophic response 41. Furthermore, mice which are partially deficient in hypoxia-inducible factor 1 show impaired development of polycythaemia, right ventricular hypertrophy, pulmonary hypertension and pulmonary vascular remodelling 42.

In conclusion, using a rat model of the chronic blood gas changes which occur during obstructive sleep apnoea in humans, it has been shown that chronic intermittent hypercapnic hypoxia causes an increase in haematocrit, pulmonary hypertension and right ventricular hypertrophy. However, it is unclear how these results in rats might transpose to humans with obstructive sleep apnoea, especially the degree and duration of hypoxia and hypercapnia which may cause such chronic cardiovascular changes.

	Acknowledgements

TOP Abstract Materials and methods Results Discussion Acknowledgements References

 
The authors wish to thank T. Dowling and J. Slattery for technical assistance.

	References

TOP Abstract Materials and methods Results Discussion Acknowledgements References

 

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