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1       This did not generalize to the control irritant.
2 6%, is a possible carcinogen and respiratory irritant.
3 ally to cutaneously applied phenol, an acute irritant.
4 ween protons and piperine, another vanilloid irritant.
5 ha,beta unsaturated aldehyde and respiratory irritant.
6 n an assay with a cockroach, proved potently irritant.
7 ied in the vapor, and acrolein is a powerful irritant.
8 airway defense against inhaled pathogens and irritants.
9 y airway exposures to allergens and chemical irritants.
10 ell as environmental and endogenous chemical irritants.
11  pungent natural compounds and environmental irritants.
12 y for behavioral responses to these chemical irritants.
13 nd mediates behavioral responses to chemical irritants.
14 pungent natural compounds, and environmental irritants.
15 ion of nociceptors by endogenous and natural irritants.
16 mach less susceptible to damage from luminal irritants.
17 lvents, welding fumes, and other respiratory irritants.
18 hich respond to numerous odorants as well as irritants.
19 xposure to allergens, pathogens, or chemical irritants.
20 tinocytes treated with certain allergens and irritants.
21 es to protect the host against pathogens and irritants.
22 rs chronically exposed to moderate levels of irritants.
23 after chronic exposure to moderate levels of irritants.
24 ons or exposure to allergic and non-allergic irritants.
25 hagous fluids, environmental xenobiotics and irritants.
26 ent of TRPA1, a key sensor for environmental irritants.
27  in increased penetrability to allergens and irritants.
28 matory responses to cutaneous and peritoneal irritants.
29 oxyethylene) ammonium chloride (ITDOP); mild irritants: 5% 3-decyloxypropyl-bis(polyoxyethylene) amin
30               Test materials included slight irritants: 5% sodium lauryl sulfate (SLS), polyoxyethyle
31 alkylbenzene sulfonate (LAS); and a moderate irritant: a proprietary detergent (DTRGT).
32 o enhance permeability and susceptibility to irritants; accordingly, increased attention should be gi
33 rritation response in mice elicited by smoke irritants (acrolein, acetic acid, and cyclohexanone).
34          Treatment was associated with local irritant adverse effects.
35 ral, bacterial, and nonmicrobial (toxins and irritants) agents, resulting in production of many diffe
36 though the intestine is routinely exposed to irritant alimentary compounds and inflammatory mediators
37 rosols with increasing doses of the chemical irritants allyl isothiocyanate (AITC; also known as must
38  is opposite of that associated with another irritant, ammonia fumes, which elicited an increase in t
39                                     The lung irritant, ammonia, obtained as vapor over a 30% solution
40                                  Despite the irritant and allergenic properties of fungi, early-life
41 mediated, anti-inflammatory activity in both irritant and allergic contact dermatitis animal models.
42 tivated receptor-alpha agonists in models of irritant and allergic contact dermatitis produced in mou
43 R, GW3965, were examined utilizing models of irritant and allergic contact dermatitis.
44 onest forms of occupational skin disease are irritant and allergic contact dermatitis.
45 ay potent anti-inflammatory activity in both irritant and allergic contact models of dermatitis, requ
46 IV hypersensitivity, in part due to the dual irritant and antigenic properties of sensitizing chemica
47 he importance of the interaction between the irritant and antigenic properties of sensitizing chemica
48 er show that PAP-1 is not a sensitizer or an irritant and exhibits no toxicity in a 28-day toxicity s
49 jury measured at day 1, regardless of ocular irritant and the stromal response measured by the area u
50 nded chemical data set, comprising five skin irritants and 11 contact allergens.
51 s can affect airway inflammatory response to irritants and allergens, but the importance of stress in
52 r challenges, including allergens, exercise, irritants and aspirin.
53 uction machinery through which environmental irritants and endogenous proalgesic agents depolarize no
54 ormal breathing by a myriad of environmental irritants and infectious insults.
55 cautions should be taken against respiratory irritants and molds and to prevent children from becomin
56 acts as a sensory receptor for environmental irritants and oxidants.
57 tion following long-term exposure to harmful irritants and pollutants, particularly in the airways.
58 el is the molecular target for environmental irritants and pungent chemicals, such as cinnamaldehyde
59 hat they can be activated by various inhaled irritants and/or cold air.
60 pecific allergen sodium lauryl sulfate as an irritant, and appropriate controls.
61   Expression is also activated by a chemical irritant, and is suppressed by topical administration of
62 condary ozonides (SOZ), which are known skin irritants, and a modest change in particle size.
63 PCR analyses of multiple chemical allergens, irritants, and non-sensitizers have identified 10 genes
64 multiple symptomatic high-level exposures to irritants; and (iii) possible IIA, that is asthma occurr
65                     Receptors for trigeminal irritants are generally assumed to be located exclusivel
66 ctivated by noxious heat, acid, and alkaloid irritants as well as several endogenous ligands and is s
67 nses in an oxidative stress-induced model of irritant asthma.
68 ons to aeroallergens, contact allergens, and irritants at days 2, 3, and 4.
69 side' world from potentially harmful toxins, irritants, bacteria and other pathogens that also exist
70 gions in the mouth are uniquely sensitive to irritants because they can penetrate through the tissue
71 s sensory detection of pathogens, toxins and irritants; breakdown of the epithelial barrier is associ
72 ubstances, toxins, venoms, and environmental irritants but that also trigger exuberant allergic react
73                            Detection of such irritants by the trigeminal nerve evokes protective refl
74 ow a strong potentiation of responses to the irritant capsaicin in an acidic environment.
75 s thermal stimuli, protons, and the alkaloid irritant capsaicin open the channel.
76  by noxious heat, acidic pH and the alkaloid irritant capsaicin.
77                                       Airway irritants cause a variety of lung pathologies.
78 rs after treatment, mild and moderate ocular irritants caused a significant increase in corneal thick
79 he epithelium, whereas the mild and moderate irritants caused complete epithelial cell loss with incr
80         On day 1, mild, moderate, and severe irritants caused complete loss of epithelium and disappe
81 nvestigate the kinetics of both allergic and irritant CD (ACD and ICD) in vivo.
82 nsitive to mechanical stimuli and a range of irritant chemicals (bradykinin, capsaicin, low pH, plate
83           Here we show that noxious heat and irritant chemicals elicit robust escape behaviors in the
84  the tested compounds, i.e., strong and weak irritant chemicals selected from the literature, induced
85 s of the reactive hapten urushiol and by the irritant chemicals sodium lauryl sulfate and PMA.
86                                              Irritant chemicals triggered rapid ATP and ADP release f
87 ated by a range of noxious stimuli including irritant chemicals, acids and heat.
88 rnatants treated with either urushiol or the irritant chemicals.
89 narily conserved detector of temperature and irritant chemicals.
90 nflammation via hapten-specific T cells) and irritants (chemicals that are toxic to epidermal cells).
91                            The environmental irritant chloroform, a naturally occurring small volatil
92 tinocytes treated with certain allergens and irritants, compared with untreated keratinocytes.
93 apsaicin is unique among naturally occurring irritant compounds because the initial neuronal excitati
94 opic dermatitis (AD) as well as allergic and irritant contact dermatitis (ACD, ICD) are characterized
95           Atopic dermatitis (AD), as well as irritant contact dermatitis (ICD) and allergic contact d
96  In AD patients, there is often a coexisting irritant contact dermatitis (ICD) or allergic contact de
97 rs responsible for the signs and symptoms of irritant contact dermatitis (ICD).
98 flammation and condition immune responses in irritant contact dermatitis and atopic dermatitis.
99  phorbol 12-myristate-13-acetate, a model of irritant contact dermatitis and oxazolone, a model of al
100                 We report 7 cases of erosive irritant contact dermatitis due to chlorhexidine glucona
101                    Furthermore, allergic and irritant contact dermatitis reactions were exaggerated i
102 cterized by either inflammation alone (acute irritant contact dermatitis, acute allergic contact derm
103 eratinocytes, especially during allergic and irritant contact dermatitis, however, is less well under
104 morphine had no effect on croton oil-induced irritant contact dermatitis, indicating that morphine's
105 he amelioration of the phorbol ester-induced irritant contact dermatitis.
106 m dodecyl sulfate is a well-known inducer of irritant contact dermatitis.
107 iolet-B-induced skin cancers or allergic and irritant contact dermatitis.
108 C motif ligand 1 (CXCL1) in a mouse model of irritant contact dermatitis.
109 sponses in BALB/c mice to oxazolone, but not irritant contact hypersensitivity responses to croton oi
110 elements in the pathogenesis of allergic and irritant contact hypersensitivity.
111  acute stress has no effect on the course of irritant contact sensitivity, an immune reaction that do
112  continuum of irritation that can be termed "irritant contact stomatitis." This may be due to the fac
113 d having a significantly greater effect than irritant control (p < 0.001); however, neither applicati
114 ans retinoic acid, 5% sodium lauryl sulfate (irritant control), or vehicle were applied under occlusi
115 and bulb may provide an avenue whereby nasal irritants could affect processing of coincident olfactor
116 nstrated that both spontaneous and augmented irritant dermatitis in FVB.delta(-/-) mice were down-reg
117                                       During irritant dermatitis induced by topical application of cr
118                                              Irritant dermatitis is the most common cause of diaper d
119                                              Irritant dermatitis represents innate inflammatory respo
120                                              Irritant dermatitis was induced by applying phorbol 12-m
121            Neither spontaneous nor augmented irritant dermatitis was observed in FVB.beta(-/-) delta(
122 ses (e.g., psoriasis, atopic dermatitis, and irritant dermatitis) triggered by abnormal barrier funct
123 hogenic role for keratinocyte-derived ATP in irritant dermatitis, they also form the basis for a form
124 ocytes may serve as a causative mediator for irritant dermatitis.
125  mouse models of atopic dermatitis and acute irritant dermatitis.
126 emoresponsive capabilities of the trigeminal irritant-detection system.
127 ymethane and subsequently exposed to colonic irritant dextran sodium sulfate (DSS).
128 clinician be aware of cutaneous mimickers of irritant diaper dermatitis as well as their treatments.
129  nasal epithelium, requiring that trigeminal irritants diffuse through the junctional barrier at the
130 ave been identified, including environmental irritants (e.g., acrolein) and ingredients of pungent na
131  (e.g., allyl isothiocyanate), environmental irritants (e.g., acrolein), and endogenous ligands (4-hy
132  nerve endings can detect certain lipophilic irritants (e.g., mints, ammonia), the epithelium also ho
133 gic contact dermatitis, and suggest that the irritant effect of chemicals may be mediated through the
134 h PBS or OVA-peptide, indicating a potential irritant effect of drop application.
135 tionally attributed to immunosuppressive and irritant effects of CS on human cells.
136             The nAChR subtype transduces the irritant effects of nicotine in tobacco smoke and, in ce
137 patients, who may be more susceptible to the irritant effects of these dressings.
138 e (CYP) which is metabolized to acrolein, an irritant eliminated in the urine.
139  various clinical forms of asthma related to irritant exposure at work.
140              The causal relationship between irritant exposure(s) and the development of asthma can b
141 matory conditions provoked or exacerbated by irritant exposure.
142 d by subcutaneous injections of the chemical irritant formalin substantially increased the release of
143 n excitatory ion channel targeted by pungent irritants from mustard and garlic.
144  with accidental exposures to high levels of irritant gases depended on cumulative levels of pulp mil
145 s, microbial products and sterile endogenous irritants governs whether the outcome will be with suppr
146                                Plant-derived irritants have predominated in this regard, but animal v
147 vironmental and occupational sensitizers and irritants in its pathogenesis and the interaction with b
148  exposed to a range of physical and chemical irritants in the environment that are known to trigger a
149 eurons and are activated by several chemical irritants in vitro.
150 igeminally mediated reflex reactions to some irritants including acyl-homoserine lactone bacterial qu
151  where it acts as a sensor for environmental irritants, including acrolein, and some pungent plant in
152 mediators and to a diverse array of volatile irritants, including those found in tear gas and garlic.
153                                     The term irritant-induced (occupational) asthma (IIA) has been us
154 ier against water loss and pathogen/allergen/irritant invasion.
155       Control of environmental allergens and irritants is essential.
156  injury, information on possible etiology of irritants is very important.
157 a known human carcinogen and mucous membrane irritant, is emitted from a variety of building material
158 ature of bronchial asthma, and inhalation of irritants may facilitate development of nonallergic AHR.
159        These data suggest that allergens and irritants may, in part, break peripheral tolerance by th
160 , but not prevented, by elimination of local irritants, meticulous oral hygiene, and regular periodon
161 ave examined in vivo and in vitro effects of irritants, most focused on events developing hours to da
162   Intramuscular injection of an inflammatory irritant, mustard oil (MO), induces significant edema fo
163 by the same injury [application of a C-fiber irritant, mustard oil (MO), to the hindpaw].
164 e-activity relationships in analogues of the irritant natural product capsaicin have previously been
165 th exposures to fungal taxa considered to be irritant or allergenic in sensitive subjects, yeasts in
166 osures are assumed to provoke wheeze through irritant or allergenic mechanisms, little is known about
167 ve types of cutaneous inflammation caused by irritant or allergic chemicals.
168                                              Irritant or allergic contact dermatitis usually presents
169 n and mycalamide, psymberin does not display irritant or blistering activity.
170 oduction of mineralization in response to an irritant or parasite threat to the mantle organ.
171  cancer, PICCs were rated as appropriate for irritant or vesicant infusion, regardless of duration.
172 itial management includes avoiding causative irritants or allergens (e.g., by wearing impermeable glo
173 s) may increase the risk of LRI by acting as irritants or through increasing susceptibility to infect
174 unds attenuate pain behavior in a trigeminal irritant pain model that is known to rely on TRPV4 and T
175 ion-specifically dead cells and a variety of irritant particles, including crystals, minerals, and pr
176 ls but not to microbial molecules or sterile irritant particles.
177  and clears the airways and lungs of inhaled irritants, particulates, pathogens, and accumulated secr
178 anate (AITC; aka, mustard oil) is a powerful irritant produced by Brassica plants as a defensive trai
179 e trees' because their anesthetic or counter-irritant properties render them useful in the treatment
180      For the skin, Doxil is classified as an irritant rather than a vesicant.
181                                              Irritant reactions can closely resemble allergic ones, a
182  care products have been documented to cause irritant reactions in susceptible individuals, particula
183 sorders varying from straightforward topical irritant reactions, such as those to synthetic pyrethroi
184 tial channel vanilloid subtype 1 (TRPV1), an irritant receptor for capsaicin, the pungent ingredient
185 te that HQ is an activator of the peripheral irritant receptor transient receptor potential (TRP) cat
186  acidosis activates and sensitizes the human irritant receptor TRPA1 (hTRPA1).
187 be distinguished within the wide spectrum of irritant-related asthma: (i) definite IIA, that is acute
188      Effects of acetaminophen on oxidant and irritant respiratory tract responses to environmental to
189                                           An irritant response induced by chronic exposure of mouse s
190 , acetaminophen greatly increased the reflex irritant response to ETS.
191 own to be integral to a CHS but not an acute irritant response, whereas CD44 does not significantly c
192  and/or potentiates the oxidative stress and irritant responses to an inhaled oxidant: environmental
193 eloped an in vitro assay for potential human irritant responses via the skin, employing human passage
194 oscopy showed that application of the slight irritant resulted in decreased epithelial thickness at 3
195 at are presumably involved in signaling oral irritant sensations.
196 ent receptor potential ankyrin 1 (TRPA1), an irritant-sensing channel.
197                                  TRPA1 is an irritant-sensing ion channel expressed in airway chemose
198 sophila melanogaster orthologue of the human irritant sensor, acts in gustatory chemosensors to inhib
199                  On day 1, mild and moderate irritants showed increasing stromal cell death from 9.8+
200 o function as chemical sensor of noxious and irritant signaling.
201                     Pretreatment with a mild irritant significantly decreased intracellular calcium i
202 lls with low concentrations of ethanol (mild irritant) significantly attenuated injury induced by hig
203 y examined whether repetitive exposure to an irritant stimulant leads to desensitization and whether
204 or the local environment for the presence of irritant stimuli and, when activated, provide input to t
205 ter a single exposure to very high levels of irritant substances; (ii) probable IIA, that is asthma t
206 ess C5aRs and that exposure to environmental irritants such as cigarette smoke modulates the expressi
207                                      Various irritants such as foods, chemicals, friction, thermal/me
208                      Oxidative stresses from irritants such as hydrogen peroxide and ozone (O(3)) can
209 s and responds to a wide variety of chemical irritants, such as acrolein in smoke or isothiocyanates
210      TRPA1 is also targeted by environmental irritants, such as acrolein, that account for toxic and
211   This contrasts with most other common oral irritants, such as cinnamaldehyde, capsaicin, and alcoho
212 rodentium but not to that caused by chemical irritants, such as dextran sodium sulfate.
213                                Inhalation of irritants, such as toluene diisocyanate (TDI), stimulate
214  activity as measured by the mouse abdominal irritant test (MAIT) when dosed at 100 mg/kg, sc, but di
215 inociceptive activity in the mouse abdominal irritant test (MAIT).
216 nd 21e were very active in the rat abdominal irritant test (RAIT) with ED(50) doses of 0.38 and 0.31
217                          TNBS, an intestinal irritant that induces the development of inflammatory bo
218  stimulation on the muscle and to a chemical irritant that is known to produce pain in humans provide
219 cle beginning on page 2574), have identified irritants that activate transient receptor potential cat
220                In response to infections and irritants, the respiratory epithelium releases the alarm
221                       With the slight ocular irritants there was little or no change in corneal thick
222  can be activated by exogenous electrophilic irritants through direct covalent modification, we reaso
223 ized epithelial chemosensors that respond to irritants through the canonical taste transduction casca
224  vivo CM revealed corneal injury with slight irritants to be restricted to the epithelium, whereas th
225  Thus, in CF, the reduced ability of mucosal irritants to stimulate airway gland secretion via SubP m
226 y dependent on both the concentration of the irritant used and the duration of exposure and was abrog
227 ociceptors and is sensitive to noxious heat, irritant vanilloids, and protons.
228        In summary, repetitive exposure to an irritant vapor results in a specific desensitization to
229 show opposing outcomes of CD39 deficiency in irritant versus allergic contact dermatitis, reflecting
230 , that is activated by a variety of reactive irritants via the covalent modification of cysteine resi
231 ndin inhibitor (indomethacin) or if the mild irritant was administered in calcium-free media.
232         The protection conferred by the mild irritant was directly dependent on both the concentratio
233 ed with sodium lauryl sulfate (SLS), a model irritant, were used to examine early molecular events of
234 hannels are activated by chemically reactive irritants, whereas snake and Drosophila TRPA1 orthologs
235 single or multiple high-level exposure(s) to irritants, whereas this relationship can only be inferre
236 ntration of a damaging agent, termed a "mild irritant," which by itself is not injurious, can attenua

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