Inflammatory markers: exhaled nitric oxide and carbon monoxide during the ovarian cycle.

Nitric oxide (NO) production and carbon monoxide (CO) production are increased in inflammatory lung diseases. Although there are some pieces of evidence for hormonal modulation by estrogen, little is known about exhaled NO and CO during the ovarian cycle. In 23 subjects, we measured exhaled NO and CO by an online analyzer. Significantly higher levels of exhaled NO were found at the midcycle compared with those in the premenstrual period or during menstruation. Higher levels of CO were after ovulation and reached a peak in the premenstrual phase. The lowest levels of CO were observed in the first days of the estrogen phase. In males, there was no significant variation in exhaled NO and CO. Exhaled NO and CO levels vary during the ovarian cycle in women, and this fact should be taken into account during serial measurements of these markers in the female population.

INTRODUCTION

Nitric oxide (NO) and carbon monoxide (CO) may be produced in increased amounts in various inflammatory lung diseases [1, 2]. Exhaled nitric oxide is increased in bronchial asthma [3], during upper respiratory tract viral infections [4], bronchiectasis [5], and active fibrosing alveolitis [6]. Exhaled CO is increased in asthma [7], cystic fibrosis [8], bronchiectasis [9], and respiratory tract infections in normal subjects [10]. In cystic fibrosis, NO is lower compared in healthy subjects possibly due to a reduced expression of inducible NO synthase in the airways [11].

Both exhaled NO and CO are recognized as markers of inflammation and tend to decrease during steroid treatment, making this measurement of potential value in monitoring lung inflammation [12].

Although little is known about the regulation of airway NO and CO production, indirect evidence suggests that it may be modulated by estrogen related to the ovarian cycle in women. It has been noted that asthma symptoms are less severe in midcycle when estrogen to progesterone ratio in systemic blood is highest. They worsen during menses when the ratio goes down after ovulation [13]. Kharitonov et al. have demonstrated that NO production is influenced by cyclical hormonal changes in women. There was an increase of more than 100% of peak NO at midcycle [14]. Estrogen increases the expression of endothelial NO synthase in a human bronchial epithelial cell line through a process that involves the stimulation of estrogen receptors and calcium influx [15].

Little is known about exhaled CO during the ovarian cycle. Endogenous production of carbon monoxide is increased during the progesterone phase of the ovarian cycle. This is correlated with an increased in red cell catabolism and an increased in reticulocyte counts [16]. An increased CO in subjects on contraceptive drugs may also be related to the activity of progesterone [17]. This increase in CO may be related to heme oxygenase 1 (HO-1) activation by several stimulants including hormones [17, 18]. Progesterone has been shown to increase expression of HO-1 in myometrial cells [19]. Also, endogenously generated NO induces the expression of HO-1 in vascular endothelial and smooth muscle cells [20]. This may provide protection against oxidative stress to endothelium [21]. On the other hand, CO can bind to the heme moiety of NOS and thus inhibit NO production [22].

Since both NO and CO are increasingly used as simple and noninvasive tools for monitoring airway inflammation, standardization is important especially when repeated measurements of exhaled NO and CO are made in female subjects. For this reason, we undertook a study of serial measurements of exhaled NO and CO during ovarian cycle.

METHODS

Subjects

We included 15 healthy, nonsmoking, regularly menstruating females, who were not taking any medications (including oral contraception; mean age, 34 ± 9 years). Eight healthy, nonsmoking age-matched males (mean age, 34 ± 3 years) comprised the control group. All the subjects were recruited from staff members at the Royal Brompton Hospital. A series of measurements were performed on them at frequent intervals (days 1–6, 7–12, 13–19, 20–25, and 26–31; day 1 was the 1st day of menstruation) during their ovarian cycle. Male subjects also underwent similar serial measurements. All subjects were asked to inhale room air at total lung capacity and then to exhale slowly into a tube connected directly to the NO and CO analyzer. All subjects signed a consent form, and the study was approved by the local Ethics Committee.

Exhaled NO measurements

Exhaled NO was measured by a chemiluminescence analyzer (model LR2000; Logan Research, Rochester, UK) sensitive to NO from 1 to 5,000 ppb (by volume) and with a resolution of 0.3 ppb which was designed for online recording of exhaled NO, as previously described [23]. The analyzer was calibrated using certified NO mixtures (90 and 436 ppb) in nitrogen (BOC Special Gases, Guilford, UK). Measurement of exhaled NO was made by slow exhalation (5–6 l/min) from total lung capacity for 20–30 s against a resistance of 3 ± 0.4 mmHg. Two successive recordings were taken, and plateau values were used in all calculations.

Exhaled CO measurement

Exhaled CO was measured using a chemiluminescence analyzer (model LR2000; Logan Research, Rochester, UK) sensitive to 1–500 ppm (by volume) CO adapted for online recording. The subjects exhaled slowly at total lung capacity with a constant flow (5–6 l/min) against a resistance of 3 ± 0.4 mmHg over 20–30 s [24]. Two successive recordings were made, and maximal values were used in all calculations. Ambient CO levels were recorded before each measurement and subtracted from measured values.

Statistical analysis

Data are expressed as means ± standard deviation. Differences between exhaled NO and CO levels produced during particular phases of ovarian cycle were compared with Kruskal–Wallis test.

RESULTS

Table 1 shows mean exhaled NO and CO levels from men and women. Measurements were performed during the first visit. There were no significant differences in either NO or CO levels between men and women; however, the variability was greater in women.

Table 1

Exhaled Nitric Oxide (NO) and Carbon Monoxide (CO) Levels in Sex Groups

	Male (n = 8)	Female (n = 15)	p value
Age (year)	34 ± 3	34 ± 9	>0.05
NO (ppb)	5.08 ± 1.23	5.36 ± 3.6	>0.05
CO (ppm)	3.02 ± 0.96	3.39 ± 2.87	>0.05

Means ± standard deviations are shown

There were no significant differences between repeated measurements in men (Table 2).

Table 2

Exhaled Nitric Oxide (NO) and Carbon Monoxide (CO) in Repeated Measurements in Men

	Days 1–6	Days 7–12	Days 13–19	Days 20–25	Days 26–31
NO (ppb)	5.08 ± 1.23	5.19 ± 1.6	5.34 ± 1.2	5.12 ± 1.9	4.9 ± 2.0
CO (ppm)	3.02 ± 0.96	3.3 ± 1.15	2.99 ± 1.9	3.4 ± 2.6	3.15 ± 1.7

No variability either in NO nor CO levels was observed. Mean values ± standard deviations are shown

Exhaled NO changes in expired NO levels during ovarian cycle are shown in Fig. 1. Significantly greater levels of exhaled NO were observed in the midcycle compared with those in the first third of progestational phase and premenstrual period (6.8 ± 2.17 versus 4.1 ± 1.18 and 4.3 ± 1.6 ppb; p < 0.001 and p < 0.01, respectively) and during menstruation (5.0 ± 2.11 ppb; p < 0.02).

Fig. 1

Changes of exhaled nitric oxide (NO) levels in expired air in relation to ovarian cycle. Day 1 is the 1st day of menstruation. Mean values are shown as horizontal bars.

Exhaled CO changes in exhaled CO levels in relation to ovarian cycle are shown in Fig. 2. In contrast to changes in exhaled NO levels, exhaled CO levels were not the highest in the midcycle (3.9 ± 1.67 ppm). Higher levels of exhaled CO were observed during the first third of progestational phase of the endometrial cycle (after ovulation) and reached peak values in premenstrual phase (4.4 ± 1.9 and 5.9 ± 3.28 ppm, respectively), both significantly higher than values obtained from measurements done in other phases of the ovarian cycle (p < 0.05). These were followed by a decreased in CO levels during menstruation with a significant fall in the first days of the estrogen phase (3.6 ± 2.87 and 3.1 ± 1.0 ppm, respectively).

Fig. 2

Changes of exhaled carbon monoxide (CO) levels in relation to ovarian cycle. Day 1 is the 1st day of menstruation. Mean values are shown as horizontal bars.

No correlations between exhaled NO and CO levels during ovarian cycle were found.

DISCUSSION

In this study, we have shown that exhaled NO (ENO) and CO (ECO) levels vary during the ovarian cycle. NO levels are highest in the midcycle and exhaled CO is increased during premenstrual phase. Hormone-mediated effects on basal metabolic rate and airway cell production of NO and systemic and airway production of CO may underlie changes in exhaled NO and CO.

Endogenous NO is continuously generated from l-arginine, through the action of the nitric oxide synthases including constitutively expressed neuronal and endothelial types and inducible one. The latter isoform has the greatest activity and can be induced by inflammatory cytokines, endotoxines, and viral infections. NO found in the exhaled air (ENO) reflects mainly enzymatic NO production in the respiratory tract but, in a much lesser degree, may be a result of generation of this mediator through a NOS-independent pathway (from S-nitrosothiols) [25]. Nitric oxide, found in the exhaled air, may originate from the sinuses, stomach, and lower respiratory tract. Contamination with air from the sinuses could be prevented during the measurement by exhalation against a resistance placed in the mouth, which raises the soft palate and closes the communication to the rhinopharynx. Gastric NO, even very high, in healthy subjects does not contaminate exhaled NO, as the upper and lower esophageal sphincters are closed [26]. Alteration of ENO by smoking, caffeine, nitrate, or nitrate-containing foods ingestion [27] should be prevented by abstaining from smoking and eating before the test (according to the ATS criteria) [28]. In such conditions, ENO concentration results mainly from the NO production and its release from the respiratory tract to the airway lumen and depends on the airflow rate from the distal part of respiratory tract to the mouth [29]. Both may be affected by hormones during the ovarian cycle. Kirsch et al. [15] have shown that functional estrogen receptors are expressed in human airway epithelial cells and endothelial NO synthase activity more than doubled at 5 min after exposure to physiological concentrations of estrogen [15]. It could be reflected by higher ENO concentrations in midcycle (preovulation and ovulation phases) where the estrogen concentration in the blood is the highest. Furthermore, progesterone increases resting minute ventilation during the luteal phase by central neural mechanisms [30] and augments ventilatory responses to hypoxemia and hypercapnia via an increased sensitivity of chemoreceptors [30-32]. Increased respiratory rate may result in the fall of FeNO [33], indicated in the luteal phase of our study. This may have some functional relevance. Asthma morbidity may be affected by the ovarian cycle. A study by Eliasson et al. showed that 33% of asthmatic women had significant worsening of total pulmonary symptom scores during either the premenstrual period, the menstrual period, or both with maximum increase in dyspnea, wheezing, and chest tightness during the premenstrual period [13]. Fewer symptoms were reported at midcycle when estrogen levels are highest. Moreover, estrogen treatment can be a steroid-sparing therapy in women with refractory asthma [34]. We observed the lowest levels of exhaled NO in the progestational phase when asthma symptoms usually worsen compared with those present in the midcycle. This could reflect a protective effect of NO derived from constitutive NO synthase in the airways of asthmatic patients.

In contrast to ENO, ECO reflects mainly systemic production of CO and is closely related to COHgb levels in the blood. ECO arises from the endogenous enzymatic degradation of hemoglobin (85%) catalyzed by heme oxygenase and degradation of myoglobin, catalase, and cytochromes (15%) [35]. Although the alveoli are the main place for CO elimination, ECO can be contaminated by carbon monoxide from the sinuses [35]. Through induction of HO-1, endogenous CO production could be increased by hypoxia, heavy metals, heme, exogenous CO, pro-inflammatory cytokines, hyperglycemia and hormones [36], and endogenously generated NO [20]. Thus, ECO may serve as a marker in diabetes [37], cirrhosis [38] hemoglobinopathies [39] asthma [7], cystic fibrosis [8], bronchiectasis [9], and respiratory tract infections [10]. In our study, exhaled CO levels were high in the secretory phase, reaching their highest levels in the premenstrual phase. Although a causative role in the increased blood and hemoglobin loss has been suggested to be the main source of increased CO production, there is no clear indication as to the mechanism by which exhaled CO concentration is highest in the premenstrual phase, as there is no increased hemoglobin degradation at this time. However, progesterone may significantly induce the expression of HO-1 and HO-2 mRNAs and HO-1 protein synthesis with subsequent CO production in human myometrium [19]. This has been proposed as an endogenous inhibitory mechanism of myometrial contractility during pregnancy. Since HO-1 is expressed in airway epithelial cells and macrophages, it is plausible that increased concentrations of exhaled CO in the luteal phase are also a result of HO-1 induction by progesterone.

Furthermore, in our study the lowest exhaled NO concentrations are associated with the highest CO levels. Although there are no inverse correlations between both gases, the lowest NO levels and the highest CO are observed in the progestational phase of ovarian cycle. CO can bind to the heme moiety of NOS and thus inhibit NO production [40]. On the other hand, growing evidence suggests that NO donors and NO itself induces expression of HO-1 in smooth muscle cell lines [40]. This is of a great importance in the sustained production of NO in oxidative stress providing an endogenous defense mechanism against reactive nitrogen species [41]. These two phenomena could reflect a physiologic pattern of exhaled NO and CO production. CO could be an inhibitor of airway inducible NO synthase, and this is why the lowest NO levels are observed when CO reaches its highest concentrations. On the other hand, the lowest CO levels should be associated with the highest of those exhaled NO, but this was not observed in our study. The lowest levels of exhaled CO were observed in the first days of follicular phase when NO is far from its highest values. This could indicate that the regulatory network for NO and CO production in the airways is likely to be more complex.

CONCLUSIONS

Both exhaled NO and CO are increasingly used as noninvasive indices of airway inflammation and may be useful in monitoring airway diseases. It is important to take into account the effect of the ovarian cycle on these measurements. Repeated measurements of exhaled NO and CO in women should be performed at the same time as the ovarian cycle.