Allergen free cat litter
Warning: The heater must be isolated from the gas supply piping system during any pressure testing of that system at test pressures equal to or more than 0.5 psig. Warning: Place the heater in a location where water leaks will do NO DAMAGE to adjacent areas.
In allergy skin testing, the skin is exposed to weak dilutions of different potential allergens either by pricking the skin with the allergen or using a patch taped to the skin for several days.
The allergen is so small it can remain airborne for months.
Each of the three equations is used for a number of different flow rates. The values of the three pressure drops on the right side must be given for the same flow rate.
Alone. Prasad is a panacea. Prasad is a spiritual elixir. Prasad is the Grace of the Lord. Prasad is a cure-all and an ideal `pick-me-up'. Prasad is an embodiment of Sakti. Prasad is Divinity in manifestation. Devotees of Lord Krishna should feel that every form is the form of Lord Krishna. They should not change this Bhava or mental attitude, even if a murderer appears before them to kill them. If they are established in this Bhava, the nature of the murderer will be changed or some other man will kill the murderer. If the Bhava changes, they should cultivate it again and again. Feel His Presence always. Recognise His presence everywhere. Carry His presence wherever you walk. Remember Him always. Live in Him. You need not read many books. You need not roam about in search of Gurus. You need not stand on your head for 12 years. You need not do Aswini Mudra to open the Kundalini. I have given you the essence of all Sadhanas. It is the gist of all Vedas. Practise it. Believe me. It is very easy. It will surely give you Moksha. I assure you. Those who worship Hiranyagarbha go to Brahmaloka or Satyaloka. They wait there for the life-time of Brahma. When the Brahmanda gets dissolved during the Pralaya, they enter the Supreme Self or Para Brahman along with Hiranyagarbha. Then only they lose their sense of individuality. Hiranyagarbha Upasana is the worship of the life-aspect of Ishvara. Meditation on Saguna Brahman wards off calamities. The devotee gets powers though he does not want them. Siddhis roll under his feet. He gets emancipation by successive steps. This is called Krama Mukti or progressive emancipation in contradistinction to the Sadyo Mukti or immediate emancipation attained by a Jnani. The devotee goes to Brahmaloka first and then enters into Nirguna Brahman. This is called Krama Mukti. The Jnani is absorbed into Nirguna Brahman directly. This is the difference. Saguna Upasakas or those who meditate on the image of the Lord should do Trataka first with open eyes till they can visualise a clear-cut, well-defined picture. Later on they can visualise the picture with closed eyes. The picture must be very pleasing to the mind and the eyes. It should have a good, agreeable background. When you have created a strong mental image of your Lord in the mind by continuous practice of meditation on one form, you should not disturb the mental image by changing the picture. Stick to the same picture and strengthen and feed the mental image through repeated practice of Trataka, visualisation and constant meditation on the form. Through force of habit the same mental image will appear quite easily in your mind. Sometimes you may change even your Mantra or formula when the mind is tired or wants variety, but do not change your mental image or Bhava. Do not bother yourself if you are not able to have perfect visualisation of the picture of the Lord with the closed eyes. Continue your practice vigorously and regularly. You will succeed. What is wanted is Prema for the Lord. Cultivate this more and more. Let it flow unceasingly, spontaneously. This is more important than visualisation. A piece of ordinary white paper or coloured paper has no value. You throw it away. But if there is stamp or picture of the King or Emperor on the paper currency notes ; , you keep it safe in your money purse or trunk. Even so, an ordinary piece of stone has no value for you. You throw it.
Creases lipid oxidation and gluconeogenesis from lactate but not fasting hyperglycemia or total hepatic glucose production. Diabetes 42: 1694 1699 Saloranta C, Taskinen M, Widen E, Harkonen M, Melander A, Groop L 1993 Metabolic consequences of sustainded suppression of free fatty acids by acipimox in patients with NIDDM. Diabetes 42: 1559 1566 Wilcock C, Bailey C J 1990 Sites of metformin-stimulated glucose metabolism. Biochem Pharmacol 39: 18311834 Penicaud L, Hitier Y, Ferre P, Girard J 1989 Hypoglycaemic effect of metformin in genetically obese fa fa ; rats results from an increased utilization of blood glucose by intestine. Biochem J 262: 881 885 Bailey CJ, Mynett KJ, Page T 1994 Importance of the intestine as a site of metformin-stimulated glucose utilization. Br J Pharmacol 112: 671 675 Wilcock C, Bailey CJ 1994 Accumulation of metformin by tissues of the normal and diabetic mouse. Xenobiotica 24: 49 57 Bellomo R, McGrath B, Boyce N 1991 In vivo catecholamine extraction during continuous hemofiltration in inotrope-dependent patients. ASAIO Trans 37: M324 M325 Lee A, Morley JE 1998 Metformin decreases food consumption and induces weight loss in subjects with obesity with type II noninsulin-dependent diabetes. Obes Res 6: 4753 Leslie P, Jung RT, Isles TE, Baty J 1987 Energy expenditure in non-insulin dependent diabetic subjects on metformin or sulfonylurea therapy. Clin Sci 73: 41 45 Stumvoll M, Meyer C, Mitrakou A, Nadkarni V, Gerich J 1997 Renal glucose production and utilzation. New aspects in humans. Diabetologia. 40: 749 757 Meyer C, Stumvoll M, Nadkarni V, Dostou J, Mitrakou A, Gerich J 1998 Abnormal renal and hepatic glucose metabolism in type 2 diabetes mellitus. J Clin Invest. 102: 619 624 Matthaei S, Hamann A, Klein HH, Benecke H, Kreymann G, Flier JS, Greten H 1991 Association of Metformin's effect to increase insulin-stimulated glucose transport with potentiation of insulininduced translocation of glucose transporters from intracellular pool to plasma membrane in rat adipocytes. Diabetes 40: 850 857 Matthaei S, Reibold JP, Hamann A, Benecke H, Haring HU, Greten H, Klein HH 1993 In vivo metformin treatment ameliorates insulin resistance: evidence for potentiation of insulin-induced translocation and increased functional activity of glucose transporters in obese fa fa ; Zucker rat adipocytes. Endocrinology 133: 304 311 Lalor BC, Bhatnagar D, Winocour PH, Ishola M, Arrol S, Brading M, Durrington PN 1990 Placebo-controlled trial of the effects of guar gum and metformin on fasting blood glucose and serum lipids in obese, type 2 diabetic patients. Diabet Med 7: 242245 Teupe B, Bergis K 1991 Prospective randomized two-years clinical study comparing additional metformin treatment with reducing diet in type 2 diabetes. Diabete Metab 17: 213217 Dornan T, Heller S, Peck G, Tattersall R 1991 Double-blind evaluation of efficacy and tolerability of metformin in NIDDM. Diabetes Care 14: 342344 Nagi D, Yudkin J 1993 Effects of metformin on insulin resistance, risk factors for cardiovascular disease, and plasminogen activator inhibitor in NIDDM subjects. Diabetes Care 16: 621 629 Tessari P, Biolo G, Bruttomesso D, Inchiostro S, Panebianco G, Vedovato M, Fongher C, Tiengo A 1994 Effects of metformin treatment on whole-body and splanchnic amino acid turnover in mild type 2 diabetes. J Clin Endocrinol Metab 79: 15531560 Grant PJ 1996 The effects of high- and medium-dose metformin therapy on cardiovascular risk factors in patients with type II diabetes. Diabetes Care 19: 64 66 Rains S, Wilson G, Richmond W, Elkeles R 1988 The effect of glibenclamide and metformin on serum lipoproteins in type 2 diabetes. Diabet Med 5: 653 658 Collier A, Watson HH, Patrick AW, Ludlam CA, Clarke BF 1989 Effect of glycaemic control, metformin and gliclazide on platelet density and aggregability in recently diagnosed type 2 non-insulin-dependent ; diabetic patients. Diabete Metab 15: 420 425 Josephkutty S, Potter JM 1990 Comparison of tolbutamide and metformin in elderly diabetic patients. Diabet Med 7: 510 514 and almotriptan.
Allergen blood testing
Background and Purpose--Antiplatelet agents are widely used in the secondary prevention of stroke and other vascular events. The purpose of this review is to give a perspective of the factors involved in clinical practice for selecting antiplatelet drugs appropriate to the patient population. Summary of Review--Aspirin remains the most popular drug, because it is modestly effective 25% risk reduction however, it has undesirable side effects that are sometimes serious. The nonaspirin compounds are marginally more effective but are much more expensive and subject to commercial pressures from industry. A completely new look at these compounds is necessary, rather than spending more precious resources on "drug wars" that are expensive in time and money. Conclusion--A "polypill" has been previously proposed, and possibly a combination of drugs targeted at the major vascular risk factors that is given to patients within 24 hours of initial stroke symptoms and to clearly defined patient populations may prove a solution. Stroke. 2005; 36: 2034-2036. ; Key Words: antiplatelet agents stroke management.
Conversely, if the subject’ s extended arm weakened during the test, even though you pressed down with the same amount of pressure, it means that the energy of the allergen being held by the subject has negatively impacted the energy of his body and aloxi
Several in vitro studies suggest that eosinophils may play a role in fibrosis, remodeling, and repair processes associated with IgE-mediated hypersensitivity. However, the relationship in vivo, between allergen-induced tissue eosinophilia and markers of repair has yet to be established in human atopic subjects. Using the allergen-induced cutaneous late-phase reaction as a model of allergic inflammation, we have tested the hypothesis that eosinophil-derived TGF- 1 and IL-13 are temporarily associated with myofibroblast formation and deposition of tenascin and procollagen I. Biopsies were taken from atopic volunteers at 1, 3, 6, and 72 h after intradermal allergen challenge and were examined by immunohistochemistry. Following the peak of the late-phase reaction 6 h ; there were persisting TGF- 1 eosinophils, -smooth muscle actin myofibroblasts, tenascin immunoreactivity, and procollagen-I cells 24 48 h postchallenge. Direct evidence of generation of repair markers was obtained by coculture of eosinophils and fibroblasts. This resulted in -smooth muscle actin immunoreactivity that was inhibitable by neutralizing Abs to TGF- as well as production of tenascin transcripts and protein product. TGF- 1 and IL-13 also induced tenascin expression. We conclude that TGF- 1 and IL-13, provided partially by eosinophils, contribute to repair and remodeling events in allergic inflammation in human atopic skin. The Journal of Immunology, 2002, 169: 4604 osinophils are principally regarded as pro-inflammatory cells in the pathogenesis of allergic disease and asthma through the release of lipid mediators, cytokines, chemokines, and highly charged basic proteins 1 ; . However, in allergen challenge situations such as the late asthmatic reaction, eosinophils persist after the resolution of airway narrowing. This has led to speculation that eosinophils may also play a role in wound healing, remodeling, and the development of postinflammatory fibrosis, especially as a tissue eosinophilia and eosinophil degranulation are associated with several fibrotic syndromes 2 4 ; . well documented that human eosinophils express the potent fibrogenic factor TGF- 1, and in coculture systems this cell type stimulates fibroblast proliferation, collagen synthesis, and lattice contraction 5 7 ; . addition, the Th2-like cytokines IL-4 and IL-13, also expressed by eosinophils, up-regulate fibroblast chemokine and matrix protein expression 8, 9 ; and weakly induce a myofibroblastic phenotype 9 ; . Furthermore, the selective overexpression of IL-13 in murine clara cells causes subepithelial matrix deposition 10 ; . Eosinophils also express other growth factors and cytokines that modulate mesenchymal cells, including fibroblast growth fac.
During immunotherapy, patients receive small injections containing the allergen s ; that cause their symptoms and amen.
CHAPTER VI PUBLIC FACILITIES AND SERVICES INTRODUCTION City development is dependent on a complicated network of public facilities and services. Each type of service has a unique set of constraints and must adapt to growth and change differently. This chapter focuses primarily on water, sanitation, schools, fire protection, and law enforcement, describing the various systems and their capacities and discussing their implications for the general plan. Transportation facilities and services are discussed separately in Chapter V and parks and recreational facilities are discussed in Chapter VII. GENERAL GOVERNMENT West Sacramento is a general law city with a council-manager form of government. The five-member city council consists of a mayor, selected from among the city council members, and four council members, who are all elected at large for staggered four-year terms. The City Council meets on the first, second, and third Wednesdays of every month. The City Manager is appointed by the City Council and directs the services and functions of city government. The City Council has also created several boards and commissions to assist with specific decision-making responsibilities. The boards and commissions act in an advisory capacity to the City Council and City Manager, recommend to the City Council the adoption of bylaws, rules, and regulations they deem necessary for the administration and protection of the facilities or services they represent, and perform other duties relating to the facilities or services they represent as directed by the Council. The following City Council-appointed boards and commissions are currently active in West Sacramento: Planning Commission: Seven-member body with responsibility for making recommendations to the City Council on matters regarding the General Plan and exercising responsibilities prescribed by city ordinance or resolution and state law with respect to land subdivision, planning, and zoning. The Planning Commission meets the first and third Thursdays of every month. Parks and Community Services Commission: Seven-member body which acts in an advisory capacity to the City Council on matters or issues.
Different between women receiving HMG and rhFSH in this study. It appears that neither the amount of LH nor the content of urinary contaminants present in the HMG preparation has any significant impact on oocyte and embryo quality with regard to the morphological appearance. Our results are in agreement with the findings by Jacob et al. 1998 ; and Weissman et al. 1999 ; . A very recent meta-analysis Agrawal et al., 2000 ; , after re-analysing the data of randomized trials, concluded that FSH and HMG were equally effective whenever pituitary down-regulation was used. Only in cycles without pituitary down-regulation was the use of FSH associated with a higher pregnancy rate than HMG. The role of LH in folliculogenesis, oocyte function and early pregnancy outcome during downregulated cycles has been recently challenged Fleming et al., 1998; Filicori et al., 1999; Westergaard et al., 2000 ; . The presence of LH in the gonadotrophin preparation may enhance the production of oestradiol and androgen, which play a role in oocyte maturation and embryo development. In this study, the percentage of metaphase II oocytes, normal oocyte morphology, blastomere number and embryo grading per group were calculated. It is suggested that these parameters may be better expressed per patient since it is the patient, not the oocyte, which is the independent variable Bergh et al., 1996 ; . Oocyte morphology may affect the outcome of ICSI cycles Serhal et al., 1997 ; although this is not supported by others De Sutter et al., 1996; Balaban et al., 1998 ; . Zona thickness Garside et al., 1997 ; and polar body morphology Ebner et al., 2000 ; are other important parameters in assessing oocyte and embryo quality. Morphological assessment of oocytes and embryos remains the gold standard to determine oocyte and embryo quality in clinical practice. The concentrations of hormones in the follicular fluid may reflect oocyte maturity and quality and were not examined in this study. Concentrations of oestradiol, progesterone, testosterone and LH in the follicular fluid were similar in patients who did not have features of polycystic ovaries and received HMG or rhFSH Teissier et al., 1999 ; . Other non-invasive tests such as early cleavage to the 2-cell stage Shoukir et al., 1997 ; , development of blastocyst stage, metabolic uptake of glucose and pyruvate Devreker et al., 2000 ; may also be helpful in assessing embryo quality. In conclusion, we found a similar percentage of metaphase II oocytes, normal morphology of zona pellucida, oocyte and polar body, blastomere number and grading of embryos after a long protocol of pituitary down-regulation and ovarian stimulation with either HMG or rhFSH for ICSI. Zona thickness and diameters of oocyte and ooplasma were also comparable in the two groups. HMG is as good as rhFSH in terms of oocyte and embryo quality and amevive.
Food allergen awareness week
Dose of salmeterol on the increase in airway eosin ophils induced by allergen challenge in asthmatic subjects. Thorax 1999; 54: 622 Roberts JA, Bradding P, Britten KM, et al. The long acting beta-2 agonist salmeterol xinaforte: effects on airway inflammation in asthma. Eur Respir J 1999; 14: 275 Li X, Ward C, Thien F, et al. An anti-inflammatory effect of salmeterol, a long acting beta 2 agonist assessed in airway biopsies and bronchoalveolar ravage in asthma. J Respir Crit Care Med 1999; 160: 1493 Kips JC, O9Connor BJ, Inman MD, Svensson K, Pauwels RA, O9Byrne PM. A long term study of the anti-inflammatory effect of low dose budesonideplus formoterol versus high dose budesonide in asthma. J Respir Crit Care Med 2000; 161: 996.
SCORE 2: strong and multifocal granulation SCORE 3: strong and diffuse granulation Complementary slides were prepared for AgNOR protein identification using a silver staining method and for PCNA labeling by immunohistochemistry. The NORs were counted as described by Zaczek and colleagues 30 ; . The number of NORs present in histological preparations reflects the quantity of active ribosomal genes and thus the proliferating status of tissues. This method is adequate to verify early stages of cell proliferation, including the interphase of the cell cycle, before the formation of mitotic figures. The Proliferating Cell Nuclear Antigen PCNA ; positive cells counting was performed by submitting the slides to hot high pressure followed by overnight incubation with 1 : 100 anti-PCNA antibody mouse anti-human, PC-10 clone, DAKO ; . The LSAB amplification system was also used. The slides were back stained with hematoxylin. Five microscopic fields were randomly chosen and 500 cells were counted for each slide. The PCNA method reveals the `S phase cycle' positive cells, it means, cells in the early stages of duplication. Positive cells presented strongly nuclear reactivity. The numbers of positive and negative cells were recorded. All the quantification procedures were done in blind and amoxapine.
The procedures for isolation of leukocytes from blood, for measuring the incorporation into DNA of deoxyuridine and thymidine, and for the assay of thymidylate synthetase, thymidine kinase, uridine kinase, and dihydrofolate reductase have been described in detail in earlier publications 22 ; . In corporation of the deoxyribosides into DNA was measured immediately after the isolation of the cells. The cells were disrupted by sonic oscillation, and, after centrifugation at 30, 000 X g for 25 minutes at 4C, the supernatant fluid was removed and frozen at "20C until assayed. The enzyme re actions were assayed simultaneously. Protein determination was on the sonically disrupted cells by the method of Lowry eta!. 15 ; . Drugs were administered by an intravenous pulse in the and amikacin.
Homes in the high-poverty area 20% of the population below the poverty level ; were more likely to have high cockroach allergen levels than homes in the low-poverty area , but less likely to have high levels of dust mite allergen 16 vs 53%; or, 2; ci, 1- 4.
96 Danbury Road Ridgefield, CT 06877 Ph: 203-438-9580 Fax: 203-431-8963 allergycontrol Booth #228 Continuing the 24-year tradition of allergy excellence, Allergy Control Products is excited to introduce new allergen avoidance materials at Booth 228. These include our newly improved brochure, with a comprehensive educational center section and specific action points throughout. Our educational DVD, new pamphlets and posters, along with the most effective allergy products, make Allergy Control Products the trusted source for allergen avoidance and aminoglutethimide.
Allergen statements requirementsTreatment should never be delayed for investigations, patients should never be sedated and the possibility of pneumothorax should be considered. Patients who deteriorate further despite treatment may need intermittent positive pressure ventilation and allergen
Active forms, 29 which could impair the integrity of the luminal endothelium. Because MPO-positive macrophages exist at sites of erosion of coronary plaques13 and MPO can deposit in the sub-endothelium via endothelial transcytosis, 30 local production of HOCl by MPO in the sub-endothelium of human coronary plaques may promote EC desquamation and precipitate ACS. HOCl can induce cell death by decreasing cellular ATP levels31 or modifying cell-surface proteins.32 Recently, Vissers et al demonstrated that HOCl caused apoptosis and growth arrest in human ECs, 33 and Wagner et al and Englert et al showed that MPO-derived HOCl and chloramines induced apoptosis in human leukemia cells34 and human B lymphoma cells.35 This study shows that sub-lethal concentrations of HOCl rapidly provoke apoptotic EC death, likely caused by Bcl-2 degradation and cytochrome-C release from mitochondria. We originally found that HOCl rapidly decreased Bcl-2 levels in human ECs. The precise mechanisms of HOCl-induced Bcl-2 loss remain uncertain at present. Celli et al demonstrated that intracellular GSH-depletion caused by buthionine sulfoximine could induce degradation of the Bcl-2 protein and promote apoptosis in cholangiocytes.36 We found that HOCl rapidly decreased the intracellular GSH levels in human EC, suggesting that GSH-depletion by HOCl might play a key role in the degradation of Bcl-2 protein in EC. Xue et al have shown that locally-generated reactive oxygen species can directly destroy native Bcl-2 protein by a protease-independent mechanism.37 Thus, Bcl-2 may be a direct or indirect intracellular target of HOCl, triggering the activation of the apoptotic cascade in human EC. The normal endothelium resists thrombosis. However, increased circulating soluble TF38 and TF expression by luminal or circulating ECs39 or circulating microparticles may promote thrombosis.40 Activated or apoptotic ECs can release shed-membrane microparticles into the circulation.10, 40 We demonstrate here that sublethal concentrations of HOCl increase TF activity in human ECs. MPO has recently been shown to serve as a major enzymatic catalyst for initiation of lipid peroxidation in vivo.41 It has been demonstrated hydroperoxide-dependent activation of latent TF pathway activity42 and inactivation of TF pathway inhibitor through oxidation, 43 suggesting additional alternative mechanisms of action of MPO-generated oxidants to promote the enhanced thrombogenicity in atherosclerosis. HOCl activates EC at lower, sublethal concentrations but promotes cell death at higher concentrations. This biphasic action of HOCl may contribute to the generation of circulating TF-bearing EC microparticles in inflammatory diseases.44 HOCl can activate the transcription factor nuclear factor- B in T-lymphocytes, 45 and depletion of intracellular GSH can induce proinflammatory gene expression in lung epithelial cells.46 However, the mechanisms of EC activation by HOCl require further investigation. Treatment with GSH-MEE or a cell-permeant statin at clinically relevant concentrations increased intracellular GSH content and prevented HOCl-induced cell death and TF expression in cultured human ECs. We have previously demonstrated that GSH administration can improve coronary endothelial vasomotion; 47 moreover, a polymorphism in a and aminophylline.
Air allergen reducer
Animals All animals used in this study were born and raised for at least 6 mo at LABS of Virginia, Yemassee, SC. On arrival at East Carolina University, the animals were group housed in the Department of Comparative Medicine. Animal husbandry was conducted under US Department of Agriculture guidelines. All protocols were approved by the Institutional Animal Care and Use Committee of East Carolina University. Protocols Three- to 4-yr-old adult ; animals. Seven animals, 34 yr old, were evaluated for sensitivity to aerosolized histamine and airway inflammation via differential cell counts of bronchoalveolar lavage BAL ; fluid. The animals were then sensitized by bimonthly subcutaneous injections of allergen adsorbed to alum [312 arbitrary units AU ; of Dermatophagoides pteronyssinus Dp ; and Dermatophagoides farinae Df ; extract, Greer Laboratories, Lenoir, NC; Imject alum, Pierce, Rockford, IL] for 4 mo. As originally conceived, the protocol called for the animals to receive three aerosol dust mite challenges at 1-mo intervals to establish chronic inflammation before the asthmatic response was characterized. However, the animals exhibited significant distress during the first aerosol dust mite challenge, so the protocol was modified as follows. Six weeks after the first dust mite challenge, the subjects were boosted by subcutaneous injection with allergen extract in alum. Two weeks later, responses to aerosolized histamine were determined, the lungs were lavaged, and differential cell counts of BAL fluid were acquired. Twenty-four hours later, the animals were challenged with aerosolized dust mite, and the early asthmatic response was measured. Forty-eight hours after the dust mite challenge, the histamine challenge and BAL were repeated. Neonatal animals. Fifteen animals were injected with allergen 312 AU of Dp and Df extract adsorbed to alum ; within 24 h of birth, once per week for an additional 4 wk, and then twice per month until 6 mo of age. At 8 mo age, the subjects were boosted by subcutaneous injection with allergen extract in alum. Two weeks later, responses to aerosolized histamine were determined and the lungs were lavaged for differential cell counts. Twenty-four hours later, the animals were challenged with aerosolized dust mite, and the early asthmatic response was measured. Forty-eight hours after the dust mite challenge, the histamine challenge and BAL were repeated. Eight animals were sham-sensitized by subcutaneous injection of saline on the same schedule used for sensitizing to allergen. After the initial characterization, the animals were allowed to recuperate for 9 wk before being separated into cohorts for additional characterization of late-phase responses to dust mite and responses to steroid and -adrenergic agonist therapies. Responsiveness to steroid therapy was assessed by use of a sequential protocol in which all subjects were treated with vehicle in the first leg and dexamethasone in the second leg. This ensured that inflammation and pulmonary function had returned to baseline at the time the protocol began. The subjects were boosted by inhalation of allergen 200 AU ml for 4 min ; . Two weeks later, sensitivity to aerosolized histamine was determined and BAL samples were collected. The animals were treated daily for 3 days with vehicle or dexamethasone 1 mg twice day orally ; . On the fourth day, the animals received the morning treatment via intramuscular injection, were intubated, and then were challenged with 200 AU ml 1: dilution ; of dust mite delivered through a Devilbiss ultrasonic nebulizer for 4 min. Dynamic lung compliance Cdyn ; and airway resistance Raw ; were monitored for 6 h. Oral treatments were continued until the morning of the sixth day, when the treatment was given by intramuscular injection. Sensitivity to aerosolized histamine was reassessed and the lungs lavaged. A 3-wk washout period separated the vehicle and dexamethasone legs of the study.
Daily allergen index
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