USE OF GUAIFENESIN FOR INHIBITING MUCIN SECRETION
BACKGROUND OF THE INVENTION
Ϊ . Field of the Invention
The present invention relates to the use of a pharmaceutical compound for the inhibition of mucus secretion in an individual.- in particular, the present invention relates to the use of guaifenesin for the inhibition of mucus secretion.
2. Description of Related Art
Guaifenesin, whose chemical name is 3- 2-methoxypheno y)- 1 ^-propanediol, · is an expectorant. An expectorant is a drug that helps bring up mucus and other material from the lungs, bronchi, and trachea. Guaifenesin is thought to act by thinning the mucus, loosening phlegm and bronchial secretions, and also by lubricating the irritated respiratory -tract By thinning, the mucus, guaifenesin reduces the viscosity of the- mucal. secretions, and as a result increases the efficiency of the cough reflex and of ciliary action in removing accumulated secretion's from trachea -and bronchi. The effect felt by an individual is that a nonproductive cough becomes more productive and less frequent.
In the prior art there are disclosed methods of inhibiting mucin. However, these methods are directed to the treatment of chronic conditions, suc --as asthma. 'WO 2004/043392 discloses a method of modulating mucin synthesis and the therapeutic- application of compounds in controlling mucin over-production associated with diseases such as chronic obstructive pulmonary diseases (CGPP), including chronic bronchitis, and, inflammatory lung diseases, asthma, cystic fibrosis and acute or chronic respiratory infectious diseases using compounds of a defined formula having at least two aromatic rings.
BRIEF SUMMARY OF THE INVENTION
The applicant has developed a method of inhibiting the secretion of mucus in an. individual which comprises administering an effect ve amount of a composition- -which comprises guaifenesin..
According to a first aspect of the present invention there is provided a method of inhibiting rmicus secretion in an individual which comprises administering an effective amount.
•of a composition which comprises guaifenesin. The composition can contain from approximately 600mg- 1200mg o f guai fenesin.
The guaifenesin can be administered in many suitable forms such as a tablet, powder, capsule, liquid or liquigel. The guaifenesin can be administered orally.
The mucin can be produced in the upper respiratory tract of an individual.
Tire composition can contain one or more additional active agents selected from the group including, but. not limited to, an antitussive such as dextromethorphan hydrobromide, a decongestant such as phenylephrine hydrochloride, pseudoephedrine hydrochloride or■ephedrine, •an antihistamine such as chlorpheniramine maieate, brompheniramine maieate, phenindamine tartrate, pyrilamine maieate, doxylamine succinate, phenyitoloxamine citrate, diphenhydramine hydrochloride, promethazine, and clemastine fumerate. fexofenadine or a combination thereo
The composition can have an immediate release portion and a sustained release poition, such that the inhibition of mucus secretion, is therapeutically achieved for a period of approximately ί 2 hours.
The daily dose of guaifenesin can be 24O0mg.
According to a second aspect of the present invention there is provided a method of treating an individual having a disease or condition characterized by increased mucin secretion with an effective amount of a composition which comprises guaifenesin as described in the first aspect of the present invention.
The disease of condition characterized by -increased mucin secretion infectious can be selected from inflammatory conditions of the airways.
BRIEF DESCRIPTION OF THE FIGURES
Example embodiments of the present invention will now be described in more detail with reference to the accompanying figures.
Fig, 1 illustrates the treatment protocol.
Fig. 2 is a graph showing the effect of guaifenesin on MUC5 AC mucin secretion: 30 mm
Figs. 3a and 3b are graphs showing the effect of guaifenesin on MUC5AG mucin secretion: 6 hours
Figs. 4a and 4b are graphs showing the effect of guaifenesin on MUC5AC mucin secretion: 24 hours
Figs. Sa and 5b are graphs showing the effect of guaifenesin on MUC5AC mucin secretion: 48 hours
Fig, 6 is a graph showing the effect of guaifenesin on mucociliary clearance.
Figs. 7a and 7b are graphs showing metabolic activity.
Figs. 8a, 8 b and 8c are graphs showing mucus theology.
Figs. 9a and 9b are graphs sho wing the vector sum of viscosity and elasticity against time and dose,
DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS MATERIALS AND METHODS
Cells:
EpiAirway cultures (normal human bronchial epithelial) cells grown on Millipore Transwells, 1 or 4.2 cm2 surface area. The cells were purchased from MatTek, and were cultured, at air-liquid interface for two (mucus synthesis and secretion) or three (mucociliary transport and mucus rheoiogy) weeks prior to use.
Guaifenesin (GGE) Treatment:
For mucociliary clearance, a stock guaifenesin solution of 2 mg/mL in culture medium was prepared in the morning of each experiment, and kept cold until dilution into wanned medium to the target concentrations of 0,2, 2, 20 or 200 μg/mL. The medium in the basolateral compartment of each culture was replaced with the GGE-contammg medium, and the cultureswere returned to the 37°C, 5% CO2 incubator for as the times indicated. The experiments were repeated three times on independent cultures.
The concentrations used in the in vitro experiments range from 0.2 μg/mL to 20 mg/mL and thus bracket the clinical doses used in humans.
Measurement of Mucin Secretion:
GUAIFENESIN solutions were prepared by dissolving in PBS .(phosphate buffered saline) immediately before treatment of the cells. MUC5AC mucins were quantified by BLISA using 45MI antibody (Lab vis ion, Fremont, CA). Confluent 1 cm* NHBE cells grown on an air/liquid interface were washed from the apical surface with 200 p.L PBS and incubated with fresh, complete growth medium added to the basal chamber. Cultures were incubated 24 hours to collect the apical fluid (pretreatment sample or PT) by adding 100 PBS to the apical, surface of the cultures. PBS was added to dilute the highly viscous, thin mucus layer on the surface. Because of the .small size of the insert, it was not feasible to collect a sufficient amount of mucus for both pharmacology and rheology without the addition of PBS. After collecting 100 μΐ..· of the diluted, mucus samples (PT), cultures were divided into three groups (6 hr, 24 hr and 48 hr), 16 inserts per group, and treated with varying concentrations of guaifenesin (0, 0,2, 2, 20 ^g/mL) for each time group, 4 inserts per each dose. Thus, a total of 48 inserts were used for this study {4 inserts/dose x 4 doses/time point x 3 time points). The apical fluid was' collected at 30 minutes following drug treatment front all the cultures to see whether guaifenesin affects the "secretion" of mucins. The apical, mucus sample was collected in two steps ···· first by adding 100 μ.Ε PBS to the apical surface ( 1 st wash) and then by adding 100 μL· PBS containing 5 mM dilhiothreitol (DTT) (2"a wash). Samples from each wash were assayed for MUC5AC content and the sum of the two values (the 1st and 2™ wash.) was expressed. -as the '"released MUC5AC" of the culture. At the three different time points (i.e., 6, 24, and 48 hr), cultures were washed to collect the apical fluid as described above ("released mucin" ) and lysed using a lysis buffer (PBS, pH 7.2. 1. mM Triton. X- 100, 2 mM EDTA, 1 mM PSMF and 5 mM DTT) ("cellular mucin"). The amount of mucin in' each sample (either secreted, released, or ceil lysate) was divided fay the amount of mucin in the PT sample collected from the same well in order to obtain a "secretory index" to compensate for the variations among the cultures* The treatment protocol is depicted in Fig. ] .
Measurement of Mucociliary Clearance:
Cultures (4.2 cm.') were exposed to basolaieral guaifenesin for 1 or 6 hr. The cultures were removed from the incubator and placed on. the stage of digital imaging microscopy system . Video data were collected for 10 seconds using a. 25x objective. The rate of movement of endogenous cell, debris -was analyzed on the video images using a transparent template overlay
on the video images and a stopwatch to measure at least 5 particles on each culture, for a total of between 30 and 45 .measurements per condition.
Collection of Mucus:
Following the analysis of clearance, mucus was harvested from the apical surface of the cultures, without dilution.
Viability;
The apical surfaces of the cultures were then washed with PBS and the metabolic activity, an indicator of viability, was measured using the Water Soluble Tetrazolittm (WST) assay (Boehringer).
Rheologie Measurements:
The rheologieal properties of apical mucus secretions (20 p.L) were measured using art ARI000 controlled stress rheometer (TA Instruments:, New Castle, DE) using a parallel plate ■geometry. The dynamic linear viscoeiastk behavior was determined from the strain response to. an oscillating stress and reported as a storage or elastic modulus (C), and loss or viscous (G"j modulus, as a function of frequency co such that viscosity, ' = G'V'io. Rheologie data can also be presented using vectorial notation .as tangent δ which is the ratio of viscosity to elasticity and G*, the vector sum of viscosity and elasticity (mechanical impedance). When stress in the linear range is used to evaluate the materials, the material properties are independent of stress.
In order to conduct a frequency sweep from- 0.1 to 1000 rad/s, we evaluated viscoelasticity using a creep test at 0.5 Pa for 2 minutes. The strain response was fitted to a discrete relaxation spectrum, transformed to the retardation spectrum, and then to the storage and loss moduli, as a limciion of frequency, using metiiods developed by the PI. We evaluated the linear viscoelasticity at 1 and 100 rad/s and we used an oscillatory stress sweep and steady shear flow experiments to evaluate the behavior in the non-linear ranges. The oscillatory sweep data were analyzed by observing the stress where G' and G" crossed. This point indicates where' the material sho ws more viscous behavior '(irreversible -deformation, and flow} than, recoil behavior.
All rheologie measurements were made by technicians who were blinded, to the treatment
tatistics:
For mucin secretion, differences between control and guaifenesin treatment groups were assessed by comparing the means using Student's t-test for unpaired samples and p«G\05 was considered significant Ail the values in the figures represent means ± SEM of 4 cultures unless otherwise stated. * p<0.05, *'* p- 0.0 i
For mucociliary clearance, differences between eontrol and guaifenesin' treatment groups were assessed by comparing the means using ANOVA, with a Bonferroni post-test to assess differences from the controls tested at the same time after treatment. A p value of < 0.05 was considered statistically significant.
For rheoiogy experiments, data were analyzed using the StatView™ 5 statistics package. Raw data were visually confirmed to be normally distributed about the mean. ANOVA was used to compare results of treating sputum with, different concentrations of guaifenesin. Fisher's protected least significant difference test was done to .determine significance with multiple comparisons. Data are presented as group means ± ί standard error unless otherwise indicated. By convention p < 0.05 is considered statistically .significant.
RESULTS
In Fig. 2, EpiAirway cultures were treated with the indicated concentrations of guaifenesin for 30 min. Secreted MUC5AC was compared with the pre-ireatment values:.
During the 30 minute treatment period., there was- no -significant difference (p<0,05) between eontrol and guaifenesin treatment groups.
In Fig. 3a. the white boxes represent the amount of mucin associated with, the cell, whereas the black boxes represent the amount of mucin released during the given period of treatment. Therefore, the addition of the white box. and the black box represents the total amount of mucin produced during the given period. The total amounts ofMUC5 AC- were compared for statistical differences between control (no guaifenesin) and guaifenesin groups.
Treatment of NHB.E cells with guaifenesin .for 6 hours did not affect the amounts of mucins released (Fig. 3b). However, the total amounts of mucins produced during the 6 hour treatment period were significantly (p<0,01 ) suppressed by the presence of guaifenesin (both. 2 /ig/nil and 20 /fg/ml).
Twenty-four hour treatment with either 2 ^g/mL or 20 /ig/mL of guaifenesin significantly suppressed mucin release (Fig. 4b) as well as- mucin production (Fig.4a).
Treatment with guaifenesin (2 μ-g/mL and 20 μg/mL) for 48 hours significantly (p<0.01 ) suppressed the production of mucins (Fig.. 5a). However, the amount of mucin released during this period did not .seem to be significantly affected.
Effect of Guaifenesin on Mucociliary Clearance:
As shown in Fig. 6, guaifenesin appeared to increase the mobility of the cellular debris on the surface of cultures treated for 1 hr, but there was little evidence of a dose-response and in fact, only the effect of 2 μg/ l was statistically significant. However,, at the 6 hr time point, there was a strong trend to a dose response and movement of the -surface material for all three concentrations tested was significantly faster than the control as illustrated -in. Fig. 6,
EpiAirway cultures were treated with the indicated concentrations of guaifenesin†b.r 1 or 6 his. Mucociliary clearance was assessed, by the rate of mo vement of endogenous debris on. the surfaces. *** indicates significantly different from- the control cultures- at the same time, p < 0.00.5.
Viability:
There was no adverse effect on the viability of the cells as indicated by the WST assay. In fact, there appeared to be a- trend to increased- metabolic activity in the cells treated with guaifenesin, however this did not. reach statistical significance. Data from one of the three replicate experiments is shown below.
As shown in Figs. 7a and 7b, EpiAirway cultures were treated with the indicated concentrations of guaifenesin for 1 or 6 hr. Metabolic activity was assessed using the WST assay, .separately added to the apical or basal surfaces of the cultures.
Rheology:
A total of 96 specimens from 5 sets of experiments were analyzed. The Mucus from the first lour experiments was received at ambient temperature and. analysis of rheology of these samples showed extreme heterogeneity and the rheologic sweep curves obtained were consistent with degradation. The results shown in figures 7 and 8 are therefore derived from the- 22 specimens received from batch five. All specimens were non -Newtonian, isco elastic gels.
The results demonstrate a significant guaifenesin dose-dependent decrease in viscosity, elasticity, and complex modulus (G*) of specimens at 1 hour (p < 0.05} and- especially at 6 hours (p < 0.01 ) when measured at 1 rad/s or roughly ciliary frequency but not significantly at 100 rad/s corresponding to cough.
Mucus Rb.eofo.gy. Fig. 8a: G" viscosity. Fig. 8b: G' elasticity, Fig. 8c G* mechanical impedenee (vector sum of viscosity and elasticity). Data shown are the mean and standard error of 'data from the 1 and 6 hr time points combined..
G*: vector sum of viscosity and elasticity, at 1 rad-'s (Fig. 9a) arid 100 rad/sec (Fig. 9b), segregated by time as well as dose.
In all three treatment time periods (6, 24 and 48 hours), guaifenesin at both 2 μg/mL and 20 μg/mL suppressed the production of mucins by M'BE cei ls gro wn on. an atf/iiquid interface. Likewise, treatment with both 2 ^g/mL and 20 μg/mL of guaifenesin for 24 hours showed a significant (p<0.05) decrease in mucin release.
To address the effects of -guaifenesin on mucociliary clearance, mucociliary' transport rates were measured. The purpose of these experiments was to investigate potential alterations in .mucociliary clearance induced by exposure of differentiated primary human tracheo-hronchial. epithelial cells to Guaifenesin. The original plan was to deposit aerosolized 1 μm diameter fluorescent microspheres on the surface of -the cultures' using a nebulizer. However, for reasons that are unclear, although the microspheres eouid be identified on the cultures, there was movement in only a very few of th e 'cultures, despite clear movement of the endogenous cellular debris. A switch to collecting video of the endogenous debris was made.
Viscosity (loss modulus) is the loss of energy from a rheoSogie probe or applied, stress and thus the resistance to flow. Elasticity (storage modulus.) is the recoil energy transmitted back to the probe. The complex modulus, G*, is also known as the mechanical impedance.. As the vectoral sum of the storage and loss moduli , G* measurement indicates -resistance lo deformation. Viscoelasiieity is a property of non-Newtonian fluids (gels). Dynaraie viseoelasticity measures •the strain response of mucus to an applied stress. Because mucus is subjected- to both low -stress (ciliary beat) and high stress (cough) conditions, we measure the strain developed in response to a dynamic stress.
These results are- consistent with the secretions taken from the differentiated cells being .mucus gels. Although degradation of -specimens from experiments 1-4 produced inconsistent results suggesting degradation (raw results ail available on request), those from the final set of experiments were well preserved and the results were robust. The decrease in complex modulus .paralleling thai of the viscosity (loss modulus) would be consistent with the increased ciliary transport. The rheoiogic characteristics of these specimens suggested a -goblet cell origin with viscosity approximately equal to elasticity, rather than a submucosal gland secretion where the elasticity is generally greater than viscosity. These results are consistent with the reported structure of the EpiAirway cultures. It will he informative to compare these results with those from human tissue expi-ants exposed to guaifenesin.
G aifenesin suppressed mucin production from confluent human bronchial epitlieiial cells grown on an air-liquid interface in a dose-dependent manner in vitro at -concentrations -that are clinically relevant The reduction in mucus production correlated with increased mucociliary transport .and decreased viscoelasticity of the mucus.
Further modifications or improvements cane be made without departing-, from the scope of the invention herein described.