Treatment with (R)-α-methylhistamine or IL4 stimulates mucin production and decreases Helicobacter pylori density in the murine stomach
https://doi.org/10.5878/hg1a-sd78
The histology data show the sum scores for each group used to calculate the results in percentages normalized to non-infected vehicle-treated or H. pylori-infected vehicle-treated mice allowing for pooling results from different experiments into the same graph.
The antibody levels determined by ELISA are presented in absorbance 450nm.
The cell growth/viability was measured as the reducing potential of viable cell data presented in luminescence.
The expression of virulence factor assessed by RT-PCR is expressed in fold-change.
Documentation files
Documentation files
Citation and access
Citation and access
Data access level:
Creator/Principal investigator(s):
- Macarena P. Quintana-Hayashi – University of Gothenburg
Research principal:
Data contains personal data:
No
Citation:
Language:
Method and outcome
Method and outcome
Population:
Mice were divided into different groups: non-infected vehicle-treated control, H. pylori vehicle-treated, H. pylori-infected RaMH-treated and H. pylori-infected Il4-treated.
Time method:
Study design:
- Preclinical study
Description of study design:
This study aimed to restore mucin production in the male C57BL/6 mouse H. pylori (SS1) infection model and evaluate its effects on H. pylori density. Mice infected with SS1 were treated with (R)-α-methylhistamine (RαMH) or interleukin-4 (IL4).
Sampling procedure:
Description of sampling:
A total of 300 µl per mouse was prepared by dissolving 2.6 mg of GalNAz in 50 µl DMSO and diluted in PBS. The GalNAz injections were given intraperitoneally at 14 days post-infection, and mice were sacrificed 2 h after the injection by cervical dislocation under anesthesia with isoflurane. Whole blood samples from each mouse were collected upon sacrifice. Then, the stomachs were harvested and opened along the greater curvature followed by a gentle wash in sterile PBS to remove chyme. A stripe of the lesser curvature of the stomach containing forestomach, corpus, and antrum was fixed in buffered formaldehyde 4% aqueous solution for 24 h. The fixed tissue was paraffin-embedded and histological slides were prepared with 4 µm thick tissue ribbons.
Additionally, two pieces of the corpus (approximately 4 x 4 mm) were collected. One was placed in RNA-later, and stored at 4°C, the other one was immediately frozen in dry ice. Both samples were later stored at -80°C until use.
Time period(s) investigated:
Variables:
26
Number of individuals/objects:
86
Data collections - 4 collections
Data collections - 4 collections
Data collection - Measurements and tests
Data collection - Measurements and tests
Mode of collection:
Measurements and tests
Description of the mode of collection:
A total volume of 300 µl per mouse was prepared by dissolving 2.6 mg of GalNAz in 50 µl DMSO followed by dilution in PBS. The GalNAz injections were given intraperitoneally at 14 days post-infection, and mice were sacrificed 2 h after the injection by cervical dislocation under anesthesia with isoflurane. Whole blood samples from each mouse were collected upon sacrifice. Then, the stomachs were harvested and opened along the greater curvature followed by a gentle wash in sterile PBS to remove chyme. A stripe of the lesser curvature of the stomach containing forestomach, corpus, and antrum was fixed in buffered formaldehyde 4% aqueous solution for 24 h. The fixed tissue was paraffin-embedded and histological slides were prepared with 4 µm thick tissue ribbons. Additionally, two pieces of the corpus (approximately 4 x 4 mm) were collected. One was placed in RNA-later, and stored at 4°C, the other one was immediately frozen in dry ice. Both samples were later stored at -80°C until use.
Time period(s) for data collection:
2021-04-22 - 2021-05-06
Source of the data:
- Biological samples
Data collection - Measurements and tests
Data collection - Measurements and tests
Mode of collection:
Measurements and tests
Description of the mode of collection:
A total volume of 300 µl per mouse was prepared by dissolving 2.6 mg of GalNAz in 50 µl DMSO followed by dilution in PBS. The GalNAz injections were given intraperitoneally at 14 days post-infection, and mice were sacrificed 2 h after the injection by cervical dislocation under anesthesia with isoflurane. Whole blood samples from each mouse were collected upon sacrifice. Then, the stomachs were harvested and opened along the greater curvature followed by a gentle wash in sterile PBS to remove chyme. A stripe of the lesser curvature of the stomach containing forestomach, corpus, and antrum was fixed in buffered formaldehyde 4% aqueous solution for 24 h. The fixed tissue was paraffin-embedded and histological slides were prepared with 4 µm thick tissue ribbons. Additionally, two pieces of the corpus (approximately 4 x 4 mm) were collected. One was placed in RNA-later, and stored at 4°C, the other one was immediately frozen in dry ice. Both samples were later stored at -80°C until use.
Time period(s) for data collection:
2021-11-17 - 2021-12-02
Source of the data:
- Biological samples
Data collection
Data collection
Description of the mode of collection:
A total volume of 300 µl per mouse was prepared by dissolving 2.6 mg of GalNAz in 50 µl DMSO followed by dilution in PBS. The GalNAz injections were given intraperitoneally at 14 days post-infection, and mice were sacrificed 2 h after the injection by cervical dislocation under anesthesia with isoflurane. Whole blood samples from each mouse were collected upon sacrifice. Then, the stomachs were harvested and opened along the greater curvature followed by a gentle wash in sterile PBS to remove chyme. A stripe of the lesser curvature of the stomach containing forestomach, corpus, and antrum was fixed in buffered formaldehyde 4% aqueous solution for 24 h. The fixed tissue was paraffin-embedded and histological slides were prepared with 4 µm thick tissue ribbons. Additionally, two pieces of the corpus (approximately 4 x 4 mm) were collected. One was placed in RNA-later, and stored at 4°C, the other one was immediately frozen in dry ice. Both samples were later stored at -80°C until use.
Time period(s) for data collection:
2022-03-24 - 2022-04-09
Source of the data:
- Biological samples
Data collection
Data collection
Description of the mode of collection:
A total volume of 300 µl per mouse was prepared by dissolving 2.6 mg of GalNAz in 50 µl DMSO followed by dilution in PBS. The GalNAz injections were given intraperitoneally at 14 days post-infection, and mice were sacrificed 2 h after the injection by cervical dislocation under anesthesia with isoflurane. Whole blood samples from each mouse were collected upon sacrifice. Then, the stomachs were harvested and opened along the greater curvature followed by a gentle wash in sterile PBS to remove chyme. A stripe of the lesser curvature of the stomach containing forestomach, corpus, and antrum was fixed in buffered formaldehyde 4% aqueous solution for 24 h. The fixed tissue was paraffin-embedded and histological slides were prepared with 4 µm thick tissue ribbons. Additionally, two pieces of the corpus (approximately 4 x 4 mm) were collected. One was placed in RNA-later, and stored at 4°C, the other one was immediately frozen in dry ice. Both samples were later stored at -80°C until use.
Time period(s) for data collection:
2022-09-07 - 2022-09-22
Source of the data:
- Biological samples
Administrative information
Administrative information
Responsible department/unit:
Department of Medical Biochemistry and Cell biology
Ethical Review
Ethical Review
Reviewer:
- Swedish Ethical Review Authority
components.catalogue.resource.content.administrativeInformation.ethicalReview.rorId.srText
ROR
Registration number:
52-2021
Ethical review information:
The Göteborgs Djurförsöksetiska Nämnd (Ethic No. 52-2021) approved all experimental procedures based on the regulation from Djurskyddsförordningen DFS 2004:4.
Topic and keywords
Topic and keywords
CESSDA topic classification:
Swedish Standard Classification of Research Subjects 2025:
Publications
Publications
Citation:
Interleukin 4 induces rapid mucin transport, increases mucus thickness and quality and decreases colitis and Citrobacter rodentium in contact with epithelial cells S. Sharba, N. Navabi, M. Padra, J. A. Persson, M. P. Quintana-Hayashi, J. K. Gustafsson, et al.
Virulence 2019 Vol. 10 Issue 1 Pages 97-117
Citation:
Helicobacter pylori infection impairs the mucin production rate and turnover in the murine gastric mucosa. Navabi, M. E. Johansson, S. Raghavan and S. K. Linden
Infect Immun 2013 Vol. 81 Issue 3 Pages 829-37
DOI:
Citation:
Histological effect of (R)-alpha-methylhistamine on ethanol damage in rat gastric mucosa: influence on mucus production. Morini, D. Grandi, M. L. Arcari, G. Galanti and G. Bertaccini
Dig Dis Sci 1997 Vol. 42 Issue 5 Pages 1020-8
Metadata
Metadata
Version 1
