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Revista médica de Chile

Print version ISSN 0034-9887

Rev. méd. Chile vol.144 no.4 Santiago Apr. 2016

http://dx.doi.org/10.4067/S0034-98872016000400003 

ARTÍCULOS DE INVESTIGACIÓN

 

Reversion of methacholine induced bronchoconstriction with inhaled diazepam in patients with asthma

Bloqueo de la respuesta bronco constrictora a metacolina con diazepam inhalado en pacientes con asma

 

Mirjana Miric1,3, Sinisa Ristic2, Bojan N. Joksimovic3, Snezana Medenica4, Maja Racic4, Slavica Ristic4, Vedrana R. Joksimovic4, Mirjana Skipina4

1 Medical Faculty of the University in Pristina with temporary seat in Kosovska Mitrovica, Kosovo, Serbia, Department of pathological physiology.
2 Medical faculty Foca, University of East Sarajevo, Republic of Srpska, Bosnia and Herzegovina, Department of physiology.
3 Medical Faculty Foca, University of East Sarajevo, Republic of Srpska, Bosnia and Herzegovina, Department of pathological physiology.
4 Medical Faculty Foca, University of East Sarajevo, Republic of Srpska, Bosnia and Herzegovina.

Correspondencia a:


Background: Benzodiazepines have a direct bronchodilatory effect. Methacholine is a non-selective muscarinic receptor agonist causing bronchoconstriction. Aim: To examine the effects of inhaled benzodiazepines, modulating bronchoconstriction induced by methacholine in patients with asthma. Patients and Methods: Twelve patients with well controlled asthma were studied. On the first day, after determining the initial values of pulmonary function, a dose response curve was carried out with progressive doses of methacholine. After the last dose, when at least a 20% drop of the initial forced expiratory volume in the first second (FEV1) was achieved, vital capacity (VC) and FEV1 were measured at 7, 15 and 30 minutes after provocation. On the second day a diazepam aerosol was inhaled by the patients prior to the same protocol with methacholine. Results: In the first day of testing, methacholine inhalation (6 mg/mL) led to a significant drop in FEV1 from 2.98 to 1.69 L. On the second day of study, in the same patients, previous inhalation with diazepam reduced the changes of FEV1 after inhalation of methacholine. This parameter decreased from 2.48 to 2.21 L. Conclusions: Inhalation of benzodiazepines reduce bronchoconstriction after a methacholine challenge in patients with asthma.

Key words: Benzodiazepines; Bronchoconstriction; Diazepam; Methacholine Chloride)


Antecedentes: Las benzodiacepinas tienen un efecto broncodilatador directo. La metacolina es un agonista muscarínico que causa bronco constricción. Objetivo: Evaluar el efecto modulador de la inhalación de diazepam sobre la bronco constricción inducida por metacolina. Pacientes y Métodos: Se estudiaron 12 pacientes con asma bien controlada. En el primer día, se determinó la curva dosis respuesta de parámetros de función pulmonar a una dosis progresiva de metacolina. Después de la última dosis, cuando se consiguió un 20% de reducción en la capacidad vital forzada en el primer segundo (FEV1), se midió FEV1 y la capacidad vital (CV) a los 7, 15 y 30 min después de la provocación. En el segundo día los pacientes se inhalaron con diazepam antes de hacer la prueba con metacolina. Resultados: En el primer día, el FEV1 bajo de 2,98 a 1,69 l con 6 mg/ml de metacolina. En el segundo día, la inhalación de diazepam redujo la respuesta a metacolina con una reducción de FEV1 de 2,48 a 2,21 L. Conclusiones: La benzodiacepinas reducen la respuesta de vasoconstricción a metacolina.


 

Asthma is a chronic inflammatory disease of the airways characterized by attacks of reversible airflow obstruction that is clinically manifested by dyspnea, wheezing, chest tightness and cough. Asthma is characterized by pathological changes in the airway smooth muscle, which lead to obstruction and bronchial hyperreactivity1,2. The opposing actions of the parasympathetic and sympathetic divisions of the autonomic nervous system represent the primary mechanism for regulating airway function. It seems that the bronchial smooth muscle is normally under greater parasympathetic than sympathetic influence3. The role of the cholinergic nervous system in the regulation of muscle tone is in reflex bronchoconstriction and increased bronchial gland secretion. Acetylcholine is released from the intrapulmonary endings of vagus nerve branches and directly causes constriction of smooth muscles by stimulation of the muscarinic receptors4. Stimulation of the adrenergic sympathetic fibers causes dilation of bronchial and bronchiolar smooth muscle as well as inhibition of glandular secretion. This dilation of the airways smooth muscle is mediated by beta2 receptors1-3.

Gamma-Aminobutyric acid (GABA), is the mostwidely distributed inhibitory neurotransmitter in the mammalian central nervous system5, it binds to postsynaptic receptors, GABAA, GABAB, and GABAC, which are localized in brain and peripheral tissues including the lung6,7. GABA receptors modulate cholinergic tone or flow to the airways8. Benzodiazepines increase the activity of GABA on the level of the postsynaptic receptors and at the level of all axons in CNS. Benzodiazepines are drugs which are used as muscle relaxants, anticonvulsants and anxiolytics9-13. Methacholine acts as a non-selective muscarinic receptor agonist to stimulate the parasympathetic nervous systemand administered in vivo or in vitro mimics the effects of parasympathetic innervation of the musculature of the respiratory tract, thus causing bronchoconstriction14-16. It is most commonly used for diagnosing bronchial hyperreactivity in asthma patients using the bronchial challenge test. Through this test, the drug causes bronchoconstriction and people with pre-existing airway hyperreactivity, such as asthmatics, will react to lower doses of drug. Methacholine inhalation test also helps in the assesment of disease severity15-17. With this research we expect to demonstrate that bronchoconstrictor effects of methacholine in patients with asthma are reduced if the patient has previously inhaled benzodiazepine.

Therefore, the main purpose of our study was to examine the effect of benzodiazepines (diazepam) in modulating bronchoconstriction induced by methacholine, in patients with asthma. For this purpose, we tested: a) spirometric response of variables of lung function in bronchoconstrictor stimulus-methacholine and; b) spirometric response variables on pulmonary function in methacholine after inhalation of diazepam.

Patients and Methods

Study was carried out in the period January-July 2011. The patients were contacted for permission to be included in the study and were asked to give their written informed consent. The clinical trial included 12 patients with well controlled asthma. Clinical evaluations were conducted at the Department of pathological physiology, Faculty of Medicine in Foca, with assistence of department of pneumophtisiology at University Hospital-Foca, Republic of Srpska, Bosnia and Herzegovina. The local Ethics Commitee revised and approved this protocol.

Functional testing of respiratory system consisted of the determination of the vital capacity (VC), forced expiratory volume in first second (FEV1), Tiffeneaux index (100 x FEV1/VC), resistance to air flow in the airways (Rt) and intrathoracic gas volume (ITGV). From obtained values the specific resistance was calculated (SRt = Rt x ITGV). Obtained values for VC and FEV1 were compared with the expected table values of the European Commission for Steel and Coal (Jonasset, 1960). Functional assessment of the respiratory system is done with the help of spirometer of the “Jaeger” calibration pump and physical plethysmograph of the “Jaeger” Werzburg. Intrathoracic gas volume and resistance airway was measured by body plethysmography18.

In order to detect changes in airflow after inducing methacholine in patients with asthma, the index of bronchial reactivity was calculated. Bronchial reactivity index was defined as the log of the percent decline in FEV1/log final histamine dose after adding 10 to eliminate negative values19. Bronchial reactivity was tested by using aerosol of methacholine (Acetyl--methylcholine chloride) as inhalation test, manufactured by Sigma - Aldrich Chemie GmbH, Product Number: A2251. Methacholine was used as a solution for inhalation, at room temperature, as recommended elsewhere17.

The group of 12 asthmatic patients, which were treated by aerosol of methacholine was investigated in the course of two consecutive days:

First day: After determining the initial values of pulmonary function, dose response curve were made for the following doses of methacholine until a maximum response: 0.2, 0.6, 2.0, 6.0, and 20.0 mg/mL20. After the last dose, when at least a 20% drop of the initial FEV1 value was achieved, we measured VC, FEV1, 7, 15 and 30 minutes after provocation. Patients were in seated position and inhaled methacholine as a nebulization through the mouth. The nose was sealed with cotton wool. Each inhalation lasted two minutes and the device used for inhalation was the “Inhalet” type INHO2 (IEVT). The air flow during inhalation was 5 L/min and size of the particles obtained spray, ranged from 0.5 to 5.0 Nm. The flow of dispersed liquid was 0,2 ml/min. After each dose of inhaled methacholine, the same parameters of lung function were determined in the patients. The provocative dose (PD), by definition, is the dose that results in the desired response and represents a reflection of the sensitivity of airways. The dose of provocative substance which caused at least a 35% change in RT and SRt (proposal of the European Society for Clinical Respiratory Physiology-SEPCR) was considered clinically significant21.

Second day: The inhalation of aerosol particles, which comprised at least 10 percent by weight of diazepam (Apaurin, Krka) and less than 90 percent by weight of water, was given to the same group of patients. Vials of 10 mg/2 mL were used. The nose was closed with soft plastic clips like clothespins, which pinched the nostrils together. Benzodiazepines containing aerosols were delivered using the inhalation device “Inhalet” type INHO2 (IEVT). The device consisted of three elements: an element for heating a benzodiazepine containing composition to form a vapor; an element allowing the vapor to cool, thereby providing a condensation aerosol; and, an element permitting the patient to inhale the aerosol. The air flow during inhalation was 5 L/min and size of the particles obtained spray, ranged from 0.5 to 6.0 Nm. The flow of dispersed liquid was 0,2 ml/min. A typical dosage of a benzodiazepine aerosol is either administered as a single inhalation or as a series of inhalations taken within 5 minutes or less (dosage equals sum of inhaled amounts). After the inhalation, parameters of lung function were measured again. Then, we repeated methacholine inhalation in increased doses, in the same manner as on the previous day.

Statistical analysis of the results included the calculation of the mean value (X), standard deviation (SD) and standard error (SE) for all measured lung function parameters. To determine statistical significance, data were tested by t-test, a threshold value included changes in the level of statistical significance of p < 0.05.

Results

The population examined consisted of 12 patients with well controlled asthma in which we examined the response of the airways to increasing doses of methacholine with inhalative application of diazepam. The anthropometric data and lung function parameters are given in Table 1 and 2. Seven patients were women and five men. Their age ranged from 32 to 59 years. Only patients which FEV1 declined in more then 20% after inhalation of one of the doses of methacholine were analyzed. After application of methacholine dose of 0.6 mg/mL, six (50%) subjects responded with an increase of resistance of more than 20% after application of methacholine dose of 0.2 and 6.0 mg/ml, four patients had the same response, and two patients (16.6%) had significant bronchoconstriction to methacholine dose of 2.0 mg/mL.

 

Table 1. Anthropometric measures of patients
treated with methacholine and benzodiazepines

 

Table 2. Mean values of lung function of
asthmatic patients who are treated by methacholine
and benzodiazepine

 

The characteristic response to increasing doses of inhaled methacholine is shown in Figures 1 and 2. Figure 1 shows the effect of methacholine on the value of VC of patients with asthma, before and after inhalation of diazepam. On the first day of testing, giving methacholine provoked the dose-dependent response and reduction of VC. After inhalation of 6 mg/ml of methacholine, the values od VC significantly fell from 4.2 L to 2.7 L. Even 30 minutes after the provocation, VC values did not return to normal. However, in panel A it is shown that on the second day of testing, prior to the administration of diazepam, VC was 3.74 L in the same patient. After administration of the diazepam and methacholine (dose of 6 mg/ml), change in values of VC were significantly higher, 3.98 L, which means that VC increased and not decreased as compared to the initial value. VC was not significantly changed even after 30 minutes of testing (3.72 L) (Figure 1).

 

Figure 1. Effect of methacholine on the value of vital capacity (VC) in patients
with asthma before and after inhalation of diazepam. Panel A: On the first
day of study, methacholine given by inhalation caused dose-dependent
response, and reduction of VC. On the second day test, previously given
diazepam significantly decreased the change of VC. Panel B: shows
motion of the value in VC, and response on methacholine in relation to time
(30 minutes), before (2.7 L) and after (2.21 L) inhalation of diazepam.

Figure 2 shows the effect of methacholine on the value of FEV1 in patients with asthma, before and after inhalation of diazepam. In the first day of testing, methacholine inhalation (6 mg/mL) led to a significant drop in the value of FEV1 from 2.98 L to 1.69 L. On the second day of study, in the same patients, pretreatment with diazepam reduced the changes of FEV1, so that upon inhalation of methacoline the values of FEV1 droped from 2.48 L to 2.21 L.

Figure 2. The effect of methacholine on values of forced expiratory volume
in first second (FEV1) of patients with asthma, before and after inhalation
of diazepam. Panel A: The first day of testing, inhalation of methacholine caused
a dose dependent response and the reduction of FEV1. On the second day of
study, previously given diazepam lowered the changes of FEV1 curve.
Panel B: Shows movement of FEV1 and response to methacholine in relation
to time (30 minutes), prior to (1.69 L) and after (2.21 L) inhalation of benzodiazepines.

Figure 3 and 4 present summarized data of the relationship between VC and FEV, where patients were treated only with methacholine and methacholine with previous administration of diazepam. VC is given as a function of changes in the static parameters of lung function, FEV1 indicates a change of the dynamic parameters of lung function.

 

Figure 3. The effect of benzodiazepines on the changes of
VC induced by methacholine in patients with asthma.
On the first day of study, methacholine given by inhalation
resulted in the decrease in VC of tested patients. In the second
day of testing, a changes in VC after inhaled methacholine were
not significant, if previously benzodiazepines (diazepam) were
inhaled. Values are given as mean values of X ± SE.

Figure 4. The effect of benzodiazepines on the change in FEV1, caused
by methacholine in patients with asthma. Given methacholine resulted in
the decrease of FEV1 (p < 0.05, n = 12). On the second day of study,
the changes in FEV1 after inhalation of methacholine were not significant,
if benzodiazepines were previously inhaled in 5 minutes. (p > 0.5).
Values are given as mean values of X ± SE.

Figure 3 shows the effect of diazepam on changes of VC caused by inhalation of methacholine in patients with asthma. On the first day of study, administering methacholine reduced VC of patients (from 3.8 L to 3.1 L) (p < 0.05, n = 12). On the second day of testing, changes in VC after inhalation of methacholine were not significant if diazepam had been previously inhaled in a concentration of 1.7•10-2M, for a period of 5 minutes (p > 0.5). Values are given as mean values of X ± SE.

The graph 4 shows the cumulative change in FEV1 data, wherein the patients were only treated with methacholine and methacholine with previous administration of diazepam, FEV1 was given as a function of changes in the dynamic parameter of lung function. In Figure 4 a significant decline in FEV1 is noticeable after the administration of methacholine from 2.8 L to 1.9 L (p < 0.005). In this case, also, the FEV1 curve was normalized even after 30 min (2.2 L). The previous administration of diazepam showed no significant changes at FEV1 curve to the provocation, which means that diazepam diminished the effects of methacholine.

Discussion and Conclusions

The smooth muscle of the airways from the trachea down to the alveolar ducts is under the control of efferent fibers of the autonomic nervous system. Different typical transmitters and peptides participate in regulation of contractility of airway smooth muscle (opioid, GABA, serotonin, tachykinin and glutamat). Airway preganglionic nerve activity is regulated by subsets of pulmonary and extrapulmonary afferent nerve fibers, which continuously provide polysynaptic input to brain stem preganglionic nuclei22-24.

On the basis of our present knowledge, clinical tests and experimental studies, the hypothesis that increased cholinergic activity leads to bronchoconstriction and that it may be blocked or reduced by administering inhaled diazepam, is confirmed. Airway effector cells (bronchial and vascularsmooth muscle and glands) are densely, albeit differentially innervated by fibers derived from both the parasympathetic and sympathetic nervous system which regulate airway smooth-muscle tone, glandular secretion and blood-vessel diameter. Autonomic innervation of the airways is derived primarily from the parasympathetic nervous system1,3,24.

Benzodiazepines are drugs that have direct and indirect bronchodilatory effect on the smooth muscle of the airways, directly by inhibiting a voltage-dependent Ca²+ channels, and indirectly by increasing neurotransmision role of GABA at postsynaptic receptors, resulting in an increase in the number of open channels for chloride10-12. Benzodiazepine receptor agonists increase the affinity of GABA to its receptor. The bronchodilatory effect of diazepam indicates its potential application in the treatment of acute exacerbation of asthma25-27.

It is known that GABA-B-specific agonists decrease airway responsiveness to various bronchoconstricting agents by modulating presynaptic acetylcholine release from parasympathetic nerves. On the other hand, a GABA-B receptor agonist, baclofen, can worsen airway responses following the administration of methacholine to asthmatic patients. This paradoxical enhancement by baclofen of airway responsiveness led us to hypothesize that there may be postganglionic (i.e., smooth muscle) GABA-B functional receptors that couple to the Gi protein, known to impair relaxation of airway smooth muscle28-31. Many laboratory examinations proved that except diazepam, many other derivates of GABA for example baclofen effects on spinal respiratory neurons depending on doses. Low doses of baclofen from (0,5-2 mg/kg) increases frequency action potentials on phrenic and intercostal neurons. Middle dose of 2-4 mg/kg increases the lasting of inspiration. Higher dose 4-10 mg/kg paralyses the inspiration. The common things about these two medicines are that their effect on central neurons is dose dependent and muscle relaxant30-32.

From previous experience, it can be concluded that increased parasympathetic innervation, which leads to constriction of bronchi, becomes blocked or reduced by giving GABA or medicines that are GABA’s derivates. GABA has relaxing effect by inhibiting muscle conduction, by decreasing resistance in airway breathing channels and by decreasing contractility of trachea muscle. The same effect produce benzodiazepines by increasing GABA secretion indirectly13,23-25. Our research shows that benzodiazepines have bronchodilatory effect on the smooth muscle of the airways.

Methacholine is a synthetic choline ester that mimics the effects of parasympathetic innervation of the musculature of the respiratory tract, thus causing constriction of the bronchi. For this reason, methacholine may be used as a pharmaceutical in broncho provocation tests for the detection of bronchial reactivity3,10,15 and also for this reason we used it in this clinical trial, as a drug that provokes bronchoconstriction.

Based on this research results in patients with asthma, we conclud that the bronchoconstrictor effects of methacholine in patients with asthma is significantly reduced if the patient has previously inhaled diazepam.

 

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Recibido el 27 de abril de 2015, aceptado el 27 de enero de 2016.

Funding: This research received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.

Corresponding author: Mirjana Miric, MD, PhD,
University in Pristina with temporary seat in Kosovska Mitrovica, Kosovo, Serbia. Adress: Zoran Glodic (za Bojana Joksimovića), Ul Maka Dizdara br. 8, 73 300 Foca, Republic of Srpska, Bosnia and Herzegovina. Phone: 0038765373507
joksimovic_bojan@yahoo.com

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