Article Text

Download PDFPDF

Cerebral blood flow during treatment for pulmonary hypertension
  1. Satoshi Kusuda,
  2. Norio Shishida,
  3. Nobuhiro Miyagi,
  4. Madoka Hirabayashi,
  5. Tae-Jang Kim
  1. Department of Neonatology Osaka City General Hospital 2-13-22 Miyakojimahondori Miyakojimaku, Osaka 534-0021 Japan
  1. Dr Satoshi Kusuda. Email:skusuda{at}


AIM To determine if the haemodynamics of systemic and cerebral circulation are changed during treatment for persistent pulmonary hypertension of the newborn (PPHN).

METHODS Fifteen term newborn piglets with hypoxia induced pulmonary hypertension were randomly assigned either tolazoline infusion (Tz), hyperventilation alkalosis (HAT), and inhaled nitric oxide (iNO). Mean pulmonary arterial pressure (PAP), mean systemic arterial pressure (SAP), and cerebral blood flow volume (CBF) were measured.

RESULTS During hypoxic breathing, PAP increased significantly in all groups. After treatment PAP decreased significantly in all groups, but no significant difference was observed between groups. SAP decreased significantly only in the Tz group, and CBF reduced significantly only in the HAT group. On the other hand, iNO did not change SAP or CBF.

CONCLUSION Inhaled NO might be ideal for the resolution of pulmonary hypertension.

  • cerebral blood flow
  • pulmonary hypertension of the newborn
  • tolazoline
  • hyperventilation
  • nitric oxide

Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Several treatments for severe neonatal respiratory failure have been developed over the past decade. These include high frequency oscillatory ventilation,1 surfactant replacement,2 and extracorporeal membrane oxygenation (ECMO).3 Despite these advances, persistent pulmonary hypertension of the newborn (PPHN) remains a potentially life threatening disease with high morbidity and mortality during the neonatal period.4 5 PPHN is usually treated with tolazoline infusions (Tz) and hyperventilation alkalosis (HAT). Although both treatments have a strong effect on pulmonary vasodilatation, unexpected side effects such as systemic hypotension due to the vasodilatory action on systemic circulation and reduced cerebral blood flow due to excess hypocapnia also occur.6 7 These adverse effects could be related, in part, to the long term neurological sequelae common among survivors of PPHN. On the other hand, inhaled nitric oxide treatment (iNO) has been described as a selective pulmonary dilator in different experimental models and in human infants.8-11 iNO has recently been used for the treatment of PPHN in multicentre randomised control trials.12-14 Yet, its long term effects on the central nervous system are unknown. The influence of nitric oxide synthases on cerebral arteries and the regulation of cerebral blood flow is widely accepted.15 Thus iNO might affect cerebral circulation by altering the activity of nitric oxide synthases or changing systemic circulation. Although it is important to evaluate cerebral blood flow during iNO treatment of PPHN, only two studies using a fetal sheep or newborn lamb model have been reported.16-17

Because cerebral circulation is regulated by several factors and this autoregulation changes at different developmental stages during the perinatal period, it is important to investigate the effect of iNO on cerebral circulation of the term neonate, in whom most cases of PPHN occur. Furthermore, the newborn lamb model was induced with bacterial toxin. A different PPHN model is therefore required.

This study investigates mean pulmonary arterial pressure (PAP), mean systemic arterial pressure (SAP), and cerebral blood flow volume (CBF) during treatment for PPHN, using newborn piglets under hypoxic conditions as a model of PPHN. The hypothesis tested whether iNO, compared with other available treatments, induces selective pulmonary vasodilatation without affecting cerebral blood flow in a term newborn model of PPHN.


Fifteen newborn piglets between 1 and 3 days of age, mean body weight 2.1 kg, were given 10 mg/kg pentobarbital sodium intravenously under ether anaesthesia. After general anaesthesia each newborn piglet underwent tracheostomy and was intubated with an endotracheal tube (3.0 mm), which was secured in place. After the injection of 0.2 mg/kg pancuronium animals were ventilated using a pressure limited, time cycled ventilator (BP2001, Bear Medical Systems Inc., USA). At the start of the experiment the respiratory rate was set at 20/min, inspiratory:expiratory ratio at 1:5, PEEP at 0.4 kPa, PIP at 1.2 kPa, gas flow at 10 l/min, and FIO2 at 0.3. The respiratory rate was then adjusted to that of a PaCO2 between 5.3 and 7.3 kPa. End tidal CO2 and oxygen saturation were continuously monitored with a pulse oximeter (model 5200, Nellcore-CMI, USA). A right carotid artery catheter was inserted to allow the measurement of SAP and heart rate, using a multichannel amplifier with a thermal recorder (RMP-6018, Nihonkoden, Japan), and an electromagnetic flow transducer (1.5 mm; MVF-3100, Nihonkoden, Japan) was placed in the left carotid artery to measure CBF. Another arterial catheter was placed into the femoral artery to obtain blood samples for blood gas analysis (GEM Premier blood gas analyser, Mallinckrodt, USA). A main pulmonary artery catheter (4 Fr, Berman angiographic catheter, Arrow, USA) was inserted from the right jugular vein to measure PAP (RMP-6018, Nihonkoden, Japan). The placement of the catheter was verified by necropsy at the end of the experiment. The rectal temperature was maintained at 37.5°C with a heating blanket. Ringer solution was infused at 10 ml/kg/h into a peripheral vein. After stabilisation the FIO2 was reduced to 0.15 to produce a rise in PAP. Once PAP increased 30% above baseline, the animals were used as a model of PPHN.


The animals were randomly assigned to treatment with Tz, HAT, or iNO, and each animal received each treatment once for recording data. Tolazoline (Yamanouchi, Japan), diluted to 1 mg/ml with saline, at a dose of 1 mg/kg, was administered via an intravenous route for 3 minutes. The dose was determined from standard protocol.6For HAT, FIO2 was further reduced to 0.08, which was immediately followed by an increase in the respiratory cycle at 60/min to produce respiratory alkalosis, pH > 7.5. To maintain the same PaO2 during HAT the FIO2 was determined in experiments performed before this study. Although the PaO2remained constant, the PaCO2 fell to less than 4 kPa within 15 minutes, and that level of alkalosis was maintained. NO gas, 900 ppm balanced with N2 (Sumitomoseika, Japan), was introduced through a side connector into the inspiratory gas to produce an inhaled concentration of 30 ppm. The NO concentration was calibrated using an NO concentration monitor (PAC-NO, Dragel, Germany).


Heart rate, PAP, and SAP were continuously monitored, and CBF was measured before and after the start of each protocol. Once the monitoring values were constant, the data were recorded. Because tolazoline was administered intravenously for 3 minutes, the data were recorded at the beginning and 2 minutes after administration. After the respiratory cycle was increased for HAT, each value changed gradually. Once end tidal CO2 was constant, it was considered stable. This usually occurred between 10 and 15 minutes after the start of hyperventilation. The data were therefore recorded 15 minutes after HAT. In the case of iNO, PAP began to decrease within one minute, and reached a constant level soon after. The data were therefore recorded at the start of iNO and 5 minutes later. The timing was determined in separate experiments before this study. Arterial blood gas was analysed every time data were recorded.


All statistical analyses on recorded data were performed using StatView (Version 4.5) software (Abacus Concepts, USA). All data are presented as mean (SEM). Analysis of variance (ANOVA) for repeated measurement was used to compare the effects of treatments in each group. For comparison between groups, significant differences were tested by ANOVA at each point. Significant differences were tested with a post hoc test using the Bonferroni/Dunn correction. P values of less than 0.05 were considered significant.

This investigation was approved by the subcommittee for animal research of Osaka City General Hospital.


Table 1 shows the change in haemodynamics and blood gas analysis with a low fraction of inspired oxygen in each group. During hypoxic breathing, PAP increased significantly in all groups (p<0.01) without any significant differences between groups. SAP, however, increased slightly in all groups (not significant). CBF increased significantly with significant concomitant decrease in PaO2 across all groups (p<0.01). Heart rate, PaCO2, pH, and base excess remained constant. There were no significant differences in values between each group. Although SAP was greater than PAP, pulmonary vasoconstriction occurred during hypoxia, and further experiments to measure changes in PAP, SAP, and CBF during treatment were carried out.

Table 1

Blood gas, pH, base excess, heart rate, PAP, SAP, and cerebral blood flow volume in newborn piglets with PPHN model during treatments

PAP, SAP, CBF and blood gas variables after treatment, and differences evident before and after treatment are also summarised in table 1. During treatment PAP decreased significantly in all groups (p<0.01). However, no significant difference was observed between each group. SAP decreased significantly in the Tz group (p<0.05), CBF decreased significantly in the HAT group (p<0.01). PaCO2 and pH also changed significantly in the HAT group (p<0.01). PaO2 and base excess remained constant in all groups.


iNO is reported to have a selective pulmonary vasodilatory action and no effect on systemic circulation.8-11 The long term neurological outcomes of patients with PPHN treated by iNO, however, are not yet clear. Most patients with PPHN have already had asphyxia during the perinatal period, which can damage the central nervous system. Furthermore, hypoxia due to PPHN can worsen the damage to the central nervous system. Under these conditions, the haemodynamic change in cerebral circulation during treatments must be avoided.

Before the use of iNO becomes widespread, its effects on the central nervous system need to be investigated. The effects of iNO on CBF have been reported in fetal sheep and newborn lambs.16 17 The ability to regulate CBF in proportion to haemodynamic change is age related.18 That is, the change of CBF at the time when SAP drops or PaCO2 decreases is different for term and premature infants.

Because PPHN is more common in term infants, any changes in CBF during iNO should be investigated using a neonatal model. Furthermore, pulmonary hypertension in the newborn lamb model was induced with group B streptococci.17 The mechanism by which group B streptococci induces pulmonary hypertension is somewhat different from that in PPHN. Group B streptococci infection not only induces pulmonary hypertension but also systemic hypotension. Therefore, the effect of iNO on CBF needs to be investigated using another type of PPHN model. It is also important to compare the properties of iNO with those of other treatments whose long term outcomes are already known.

Our animal model of PPHN was created using a low oxygen tension gas mixture in newborn piglets. The pulmonary artery is very sensitive to hypoxia during the neonatal period; thus PAP can easily be increased. Furthermore, the pulmonary artery is sensitive to vasodilators. Although SAP was greater than PAP, this animal model could be used to test several treatments for PPHN.

Tz significantly reduced PAP. This, however, does not necessarily increase the effectiveness of the treatment. Tz also greatly reduced SAP; the ratio of the reduction of PAP to the reduction of SAP was almost equal. It has been reported that the use of a vasodilator cannot reduce the mortality of PPHN.19 Although Tz did not significantly diminish CBF, the sudden drop in systemic blood pressure might reduce CBF. CBF is usually constant even when the systemic blood circulation changes within a certain range because of an autoregulatory mechanism. This function is thought to be incomplete and easily impaired during the neonatal period.20 Therefore if the change in blood pressure is profound and rapid during treatment of PPHN, the CBF may also change. Because Tz is still a popular drug in many hospitals, every effort to maintain the systemic circulation must be made before administering the drug; this includes the infusion of vasoconstrictive drugs, such as dopamine, and a volume expander. This will help to avoid potential side effects such as systemic hypotension followed by the reduction of CBF.

HAT significantly reduced PAP, while not changing SAP. The reduction in PAP was the greatest achieved by all the treatments studied. Carbon dioxide tension of the artery greatly affects CBF. Hypocarbia during HAT can reduce CBF by as much as 50%.21 In our study HAT had a significant effect on CBF. After the initiation of HAT, CBF was reduced by 40%. Because CBF is regulated by many means, factors other than hypocapnia must be excluded in the experiment. As shown in table1, PaO2 did not change during HAT because of a lowered FIO2. Thus the change in CBF could not have been created by a change in PaO2.

Another factor possibly affecting CBF was an increase in MAP. After the start of HAT mean airway pressure increased from 0.4 kPa to 0.8 kPa. This increase induced a decrease in SAP and/or an increase in venous pressure and so could have affected CBF. In a different experiment we studied the effect of increased mean airway pressure on the CBF by increasing PEEP without changing respiratory rate. In this study PaCO2 remained unchanged, so we were able to evaluate the effect of mean airway pressure on CBF. The results showed less than a 10% reduction in CBF. Thus we can speculate that the huge decrease in CBF during HAT was due mainly to hypocapnia induced by HAT. Of course, we expected a reduction in CBF during HAT, but not by such a large amount (as much as 40%). The levels of PaCO2 below 4 kPa could be induced in experimental animals. Furthermore, an asphyxiated newborn infant is probably much less sensitive to a change in PaCO2 in regulating CBF.22 The changes observed in this study, however, were not small. This reduction explains the adverse outcome of patients with PPHN who are treated with HAT. HAT should only be permitted for a short duration and, as the pulmonary artery is basically sensitive to arterial pH, the pH should be maintained as high as possible with an alkaline solution.

iNO treatment of PPHN began only recently and has spread rapidly.10 11 In the present study, the selective vasodilatation of iNO was shown using a newborn piglet model. This result is consistent with previous reports of different animal models.8 9 Although the reduction in PAP was not the greatest among the treatments studied, the ratio of the reduction of PAP to SAP was the smallest. Thus the actions of iNO in PPHN might be ideal for the resolution of pulmonary hypertension, as indicated in the animal model. No effect on cerebral blood flow during iNO was observed. This result is consistent with that in the study in which fetal sheep or newborn lamb were used.16 17 Because the animal models in our study were term newborn piglets and were induced with hypoxia, the results are more accurately extrapolated to human term neonates. These results, however, were observed as an acute phase change in cerebral circulation. Thus the long term effects of iNO on CBF must be examined.

In summary, Tz had a strong effect on PAP with a strong reduction in SAP. HAT had a strong effect on pulmonary blood pressure with a strong reduction in CBF. On the other hand, iNO strongly reduced PAP without any changes in SAP and CBF. Because the reduction in CBF during treatment of PPHN is considered a major cause of subsequent brain damage, iNO is an ideal treatment for PPHN. Thus we would expect a better neurological outcome with iNO treatment than with the conventional treatments, Tz and HAT. Several control trials have demonstrated the efficacy of iNO for PPHN.12-14 Although the long term effects of iNO on newborns are unknown, iNO is a promising treatment for PPHN and could significantly reduce the mortality and morbidity associated with it.