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1.
Figure 7

Figure 7. From: Allergic lung responses are increased in prostaglandin H synthase–deficient mice.

Total IgE levels in BAL fluid of PGHS-deficient and wild-type mice. Total IgE levels in BAL fluid from nonimmunized and allergic wild-type, PGHS-1–/–, and PGHS-2–/– mice were analyzed as described in Methods. Each open circle represents results from animal. Filled circles and error bars show mean ± SE. aP < 0.001 vs. all saline control groups and wild-type OVA. bP < 0.01 vs. PGHS-2–/– OVA.

Stephen H. Gavett, et al. J Clin Invest. 1999 Sep 15;104(6):721-732.
2.
Figure 6

Figure 6. From: Allergic lung responses are increased in prostaglandin H synthase–deficient mice.

BAL fluid eicosanoid levels in PGHS-deficient and wild-type mice. BAL fluid PGE2 (a) and LTB4 (b) were determined by RIA in wild-type, PGHS-1–/–, and PGHS-2–/– mice (groups described in Figure ) as described in Methods. Each open circle represents results from 1 animal. Filled circles and error bars show mean ± SE. aP < 0.05 vs. wild-type groups and PGHS-2–/– saline groups. bP < 0.005 vs. saline-exposed wild-type and OVA-exposed PGHS-1–/– groups. cP < 0.005 vs. all other groups.

Stephen H. Gavett, et al. J Clin Invest. 1999 Sep 15;104(6):721-732.
3.
Figure 1

Figure 1. From: Allergic lung responses are increased in prostaglandin H synthase–deficient mice.

Stained cytospins of BAL fluid cells showing alveolar macrophage morphology in wild-type and PGHS-deficient mice. Wild-type, PGHS-2–/–, and PGHS-2–/– mice were administered adjuvant only and exposed to saline aerosol or sensitized with ovalbumin in adjuvant and challenged with ovalbumin aerosol. BAL cells were collected 1 day after final challenge. (a) Nonimmunized wild-type mice. (b) Allergic wild-type mice. (c) Allergic PGHS-1–/– mice. (d) Allergic PGHS-2–/– mice. ×100.

Stephen H. Gavett, et al. J Clin Invest. 1999 Sep 15;104(6):721-732.
4.
Figure 2

Figure 2. From: Allergic lung responses are increased in prostaglandin H synthase–deficient mice.

(al) Lung histopathology showing increased inflammation in PGHS-deficient mice compared with wild-type mice. (a, e, and l) Nonimmunized wild-type mice. (b and f) Allergic wild-type mice. (c, g, i, j, and k) Allergic PGHS-1–/– mice. Arrow in i indicates multinucleated giant cell. Arrow in j indicates eosinophilic crystals within macrophage. (d and h) Allergic PGHS-2–/– mice. All sections were stained with hematoxylin and eosin except k and l, which were stained with alcian blue/periodic acid-Schiff. ×10 (ad), ×40 (eh, k, and l), and ×80 (i and j).

Stephen H. Gavett, et al. J Clin Invest. 1999 Sep 15;104(6):721-732.
5.
Figure 5

Figure 5. From: Allergic lung responses are increased in prostaglandin H synthase–deficient mice.

PGHS-1 and PGHS-2 expression in nonimmunized and allergic wild-type, PGHS-1–/–, and PGHS-2–/– mice. Wild-type, PGHS-1–/–, and PGHS-2–/– mice were divided into treatment groups, and the abundance of PGHS-1 and PGHS-2 protein in the lungs was determined by Western blotting using immunospecific antibodies as described in Methods. Results are representative of experiments with 18 different animals (3 mice in each of the 6 groups). Lane 1, PGHS-1–/– mice, allergic; lane 2, PGHS-2–/– mice, allergic; lane 3, wild type mice, allergic; lane 4, PGHS-1–/– mice, nonimmunized; lane 5, PGHS-2–/– mice, nonimmunized; lane 6, wild-type mice, nonimmunized.

Stephen H. Gavett, et al. J Clin Invest. 1999 Sep 15;104(6):721-732.
6.
Figure 3

Figure 3. From: Allergic lung responses are increased in prostaglandin H synthase–deficient mice.

BAL fluid proteins are increased in allergic PGHS-deficient mice compared with wild-type mice. Wild-type, PGHS-1–/–, and PGHS-2–/– mice were divided into treatment groups and BAL fluid total protein, NAG, and LDH were determined as described in Methods. Each open circle represents results from 1 animal. Filled circles and error bars show mean ± SE. (a) BAL fluid total protein. (b) BAL fluid NAG. (c) BAL fluid LDH. aP < 0.01 vs. all nonimmunized (saline) and wild-type ovalbumin (OVA) groups. bP < 0.01 vs. PGHS-2–/– OVA.

Stephen H. Gavett, et al. J Clin Invest. 1999 Sep 15;104(6):721-732.
7.
Figure 4

Figure 4. From: Allergic lung responses are increased in prostaglandin H synthase–deficient mice.

Airway responsiveness to methacholine in PGHS-deficient and wild-type mice. Wild-type, PGHS-1–/–, and PGHS-2–/– mice were divided into treatment groups as described in Figure . Airway responses to intravenous Mch were measured 1 day after final aerosol exposure, as described in Methods. Bars represent mean ± SE of 7–13 mice per group. (a) RT before dosing with Mch and at peak of response to 25, 50, 100, and 200 μg/kg Mch (left to right for each group). For each dose, significant differences among groups were determined for associated baselines (shown above hatched bars) and increases in RT due to Mch (shown above open bars). *P < 0.05 vs. all other groups. P < 0.05 vs. wild-type saline. §P < 0.05 vs. all groups except wild-type OVA. (b) Total respiratory system-compliance (CT), measured simultaneously with RT, before dosing with Mch and at nadir of response to Mch. For each dose, significant differences among groups were determined for associated baselines (hatched bars + open bars; shown above open bars) and decreases in CT due to Mch (shown within open bars). *P < 0.05 vs. wild-type saline, wild-type OVA, PGHS-1–/– saline, and PGHS-2–/– saline. P < 0.05 vs. PGHS-1–/– saline and PGHS-2–/– OVA. §P < 0.05 vs. wild-type OVA and PGHS-1–/– saline. P < 0.05 vs. PGHS-2–/– saline.

Stephen H. Gavett, et al. J Clin Invest. 1999 Sep 15;104(6):721-732.

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