Log in

Relevant bibliographies by topics / Inflammation

Academic literature on the topic 'Inflammation'

Author: Grafiati

Published: 4 June 2021

Last updated: 22 June 2024

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the lists of relevant articles, books, theses, conference reports, and other scholarly sources on the topic 'Inflammation.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Contents

Journal articles
Dissertations / Theses
Books
Book chapters
Conference papers
Reports

Journal articles on the topic "Inflammation":

1

Vijayendranath, Nayak S., Gunasheela S, Karthik M, and Hegde Aparna. "Healing by Inflammation - Prolotherapy." Case Reports in Dental Science 1, no. 1 (June 30, 2020): 9–14. http://dx.doi.org/10.46619/crds.2020.1-1003.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Abstract:

Temporomandibular disorder (TMD) is a collective term used to describe a group of disorders related to temporomandibular region. It’s considered to be the common cause for orofacial pain. With the advancement of research, prolotherapy is considered to be the one of the treatment modalities to treat TMD, when the conservative management fails.

2

J, Mancini-Filho. "Natural Antioxidants and Tissue Inflammation." Bioequivalence & Bioavailability International Journal 7, no. 2 (July 4, 2023): 1–3. http://dx.doi.org/10.23880/beba-16000203.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Abstract:

The phenolic compounds present in food cover a wide range of structures that have different biological properties. Highlighting its antioxidant properties and the presence mainly of spices, herbs and other foods. Some compounds present in spices can be listed for their antioxidant activity, such as: cloves have eugenol, pinene in their composition, cinnamon also has eugenol, limonene, pinene, catechins and other phenolic compounds in their composition, anise has pinene, rutin, apigenin, oregano has apigenin, quercecin, rosmarinic, caffeic, p-coumaric acids, and others. Rosemary presents the carnosic, rosmarinic, caffeic and hydroxycinnamic. The tissue inflammatory process normally starts with the presence of free radicals that are associated with the oxidative process activated by reactive oxygen species represented by peroxides, superoxide ion, presence of hydroxyl radical, singlet oxygen, among others. The highlighted phenolic compounds have in their structure one or more hydroxyls that have the property of donating a hydrogen atom to free radical structures, which can block the triggering of the oxidative process and thus inflammation.

3

Djaldetti, Meir. "Piperine – An Immunomodulator and Inflammation Mitigator." Journal of Clinical and Laboratory Research 2, no. 5 (June 3, 2021): 01–04. http://dx.doi.org/10.31579/2768-0487/027.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Abstract:

Black pepper, one of the most widespread spices, gained the entitlement “King of spices” founded on its peculiar pungent test and therapeutic properties, both owed to its active alkaloid - piperine. Mounting evidence indicates that piperine possesses immunomodulatory and therapeutic activities. The aim of this mini review was to summarize the role of piperine in abolishing inflammation, its part in the immune activity of peripheral blood mononuclear- and a number of other cells, its capacity to elicit production of inflammatory cytokines and its function as a synergist endorsing the beneficial therapeutic effect of conventional anti-inflammatory drugs.

4

H, Khazaei. "Overview of Orbital Inflammation/Unmet Needs." Open Access Journal of Ophthalmology 7, no. 2 (July 1, 2022): 1–6. http://dx.doi.org/10.23880/oajo-16000245.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Abstract:

Diseases of the orbit and periorbital eye tissues manifest in a wide variety of clinical presentations. Space occupying lesions in the orbit include infections, inflammations, vascular malformations, and malignancies. The significant variation in presentations is due to the complex anatomy of the orbit and the heterogeneous nature of the multiple disease processes that present themselves as orbital inflammatory processes. Additionally, although specific disease entities often show similar patterns of orbital tissue involvement, there is still a spectrum of clinical presentations within disease processes, which furthermore overlap with other inflammatory etiologies. This heterogeneity creates a significant challenge in determining specific diagnoses and subsequently instituting timely medical and surgical management of patients with orbital inflammation. Despite advances in imaging, physical examination, and laboratory tests, a biopsy is often needed for diagnosis and to guide treatment. Unfortunately, the biopsy is too often read as non-specific or idiopathic inflammation, a term that gives minimal guidance to the patient or to the clinician. There is clearly a need for developing more specific and sensitive clinical diagnostic testing.

5

Narula, Jagat, and Eloisa Arbustini. "Inflammation, Superadded Inflammation, and Out-of-Proportion Inflammation in Atherosclerosis." JAMA Cardiology 3, no. 10 (October 1, 2018): 912. http://dx.doi.org/10.1001/jamacardio.2018.2760.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Alderton, Gemma, and Seth Thomas Scanlon. "Inflammation." Science 374, no. 6571 (November 26, 2021): 1068–69. http://dx.doi.org/10.1126/science.abn1721.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Miyamoto, Terumasa. "Inflammation." Ensho 13, no. 2 (1993): 99–100. http://dx.doi.org/10.2492/jsir1981.13.99.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Miyamoto, Terumasa. "Inflammation." Ensho 9, no. 5 (1989): 357. http://dx.doi.org/10.2492/jsir1981.9.357.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Lederer, Katy. "Inflammation." Colorado Review 43, no. 3 (2016): 128–30. http://dx.doi.org/10.1353/col.2016.0094.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Weiss, Ursula. "Inflammation." Nature 454, no. 7203 (July 2008): 427. http://dx.doi.org/10.1038/454427a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Dissertations / Theses on the topic "Inflammation":

1

Lawrence, Clifford M. "Anthralin inflammation." Thesis, University of Newcastle Upon Tyne, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.390318.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Warke, T. J. "Childhood airways inflammation." Thesis, Queen's University Belfast, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.268984.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Jatta, Ken. "Inflammation in Atherosclerosis." Doctoral thesis, Örebro : Universitetsbiblioteket, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:oru:diva-478.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Gilroy, Derek William. "Cyclooxygenase 2 inflammation." Thesis, Queen Mary, University of London, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.265077.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Limb, G. A. "Lymphokines in inflammation." Thesis, Brunel University, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373086.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Peters, Caren Lorraine. "Hypoxia in inflammation." Thesis, University of Bath, 2003. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.426151.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Sanchez, Moral Lidia. "Role of ZEB1 in adenoma formation, inflammation and inflammation-driven carcinoma." Doctoral thesis, Universitat de Barcelona, 2019. http://hdl.handle.net/10803/667993.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Abstract:

Multiple studies have highlighted the role of ZEB1 as critical regulator of tumor progression through the regulation of different hallmarks of cancer beyond the induction of EMT. The general aim of this dissertation is to characterize new potential mechanisms that regulate oncogenic transformation in colorectal carcinoma. The specific objectives of this dissertation are: 1. To identify new roles and targets of the transcription factor ZEB1 as a mediator of Wnt-induced intestinal adenoma formation. 2. To characterize ZEB1’s mechanism of action as a transcriptional regulator in inflammation and inflammation-induced carcinomas. To address these goals, a wide number of reagents and techniques have been used, namely, human samples of adenomas and CRC, CRC cell lines whose expression for different genes has been manipulated by overexpression or RNA interference, high throughput techniques (RNA and microbiota sequencing) and transgenic mouse models (ApcMin/+, Zeb1+/- and Mpg-/-). We found that ZEB1 expression in epithelial cells from intestinal adenomas increases adenoma formation and decreases life span in the ApcMin/+ mouse model, which is supported by decreased senescence and apoptosis in ApcMin/+/Zeb1+/+ mice when compared to ApcMin/+/Zeb1+/- counterparts. ZEB1 is both a target and a mediator of the Wnt signaling pathway. Here we provide two new mechanisms by which ZEB1 modulates the Wnt pathway through the regulation of AXIN2 and DACT2 expression. In addition, we found that ZEB1 promotes lipid accumulation in adenomas and colorectal cancer cell lines through the repression of the ATGL/PPARα/PGC-1α axis, which is critical for the degradation of lipid droplets. Besides, we show that ZEB1 is upregulated in the epithelial cells of ulcerative colitis patients and of mouse models of colitis, where its expression promotes intestinal inflammation and inflammatory tumorigenesis. ZEB1 exerts these functions, at least in part, through the increase of DNA damage and the inhibition of the MPG glycosylase, which is involved in DNA damage repair. Moreover, ZEB1 expression in CRC cells stimulates the production of ROS and IL1-β by macrophages which, in turn, reduce MPG expression in CRC cells. Altogether, from the results presented in this dissertation, it can be concluded that: 1. ZEB1 represses senescence and apoptosis during Wnt-induced intestinal adenoma formation. 2. ZEB1 potentiates Wnt signaling in intestinal adenomas through the activation of AXIN2 and the repression of DACT2. 3. ZEB1 induces accumulation of lipids in intestinal cells through Wnt-dependent repression of ATGL, PPARα and PGC-1α. 4. ZEB1 is upregulated in the epithelial cells of UC patients and of mouse models of colitis, where its expression promotes intestinal inflammation and inflammation-driven tumorigenesis. 5. ZEB1 promotes colitis and inflammation-driven CRC through the induction of DNA damage and the inhibition of the DNA repair glycosylase MPG. 6. ZEB1 expression in epithelial cells stimulates the production of ROS and IL1-β by macrophages that, in turn, reduce MPG expression in CRC cells. These results establish ZEB1 as an important regulator of intestinal adenoma formation, and describe ZEB1 as a mediator of inflammation and inflammation-driven carcinogenesis, setting ZEB1 as a potential therapeutic target in colorectal carcinoma.
Múltiples estudis han destacat el paper de ZEB1 com a regulador essencial de la progressió tumoral a través de la regulació de varis dels trets distintius del càncer més enllà de la inducció de la transició epiteli-mesènquima (EMT). Els resultats presentats en aquesta tesi indiquen que ZEB1 regula la formació de tumors intestinals des de les fases més inicials, i descriuen ZEB1 com un important inductor de colitis i de càncer de colon induït per inflamació. Hem trobat que l’expressió de ZEB1 en cèl·lules epitelials d’adenomes intestinals augmenta la formació d’adenomes i redueix la supervivència en el model de ratolí ApcMin/+. A més, en comparació amb els ratolins ApcMin/+/Zeb1+/+, els ratolins ApcMin/+/Zeb1+/- presenten més senescència i apoptosi. ZEB1 és tant una diana com un mediador de la via de senyalització Wnt. Els nostres resultats proporcionen dos nous mecanismes pels quals ZEB1 interacciona amb la via Wnt a través de la regulació de l’expressió d’AXIN2 i DACT2. Addicionalment, hem observat que ZEB1 promou l’acumulació de lípids a través de la repressió de l’eix ATGL/PPARα/PGC-1α, el qual té un paper crític en la degradació de les vesícules lipídiques. En paral·lel, hem demostrat que ZEB1 es troba sobreexpressat en cèl·lules epitelials de pacients de colitis ulcerativa i en models murins de colitis, on la seva expressió promou la inflamació intestinal i la tumorogènesi derivada de la inflamació. ZEB1 exerceix aquestes funcions, al menys en part, a través de l’augment de les lesions en l’ADN i la inhibició de MPG, una glicosilasa implicada en la reparació de les lesions en l’ADN. A més, l’expressió de ZEB1 en les cèl·lules de càncer de colon estimula la producció d’espècies reactives d’oxigen (ROS) i IL-1β per part dels macròfags que, a la vegada, redueix els nivells de MPG en les cèl·lules de càncer de colon. En conjunt, aquests resultats estableixen ZEB1 com un element regulador de la formació d’adenomes intestinals, així com un mediador de la inflamació i la carcinogènesi derivada de la inflamació, confirmant ZEB1 com a potencial diana terapèutica en càncer colorectal.

8

Levick, Scott P. "Inflammation and cardiovascular remodelling /." [St. Lucia, Qld.], 2005. http://www.library.uq.edu.au/pdfserve.php?image=thesisabs/absthe19090.pdf.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Blomgran, Parmis. "Inflammation and tendon healing." Doctoral thesis, Linköpings universitet, Avdelningen för Kirurgi, Ortopedi och Onkologi, 2017. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-142349.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Abstract:

Tendons heal through three different overlapping phases; the inflammatory, proliferative and remodeling phase. Many studies have investigated what factors influence healing of tendons. However, little was known about inflammation and the immune cells present during Achilles tendon healing by the time this thesis started. We developed a flow cytometry method for our rat model of tendon healing, which enabled us to study different leukocyte subpopulations during Achilles tendon healing. The general aim of this thesis was to understand more about inflammation and the immune cell populations present during tendon healing and how the immune cell composition changes during normal tendon healing. Moreover, we investigated how different factors that are known to influence tendon healing affected the composition of the immune cell population. First, we described the immune cells during the time course of tendon healing focusing on different subpopulations of macrophages and T cells. Then, we studied how these cells were influenced by reduced mechanical loading. Mechanical loading prolonged the presence of M1 macrophages and delayed the switch to regulatory T cells and M2 macrophages compared to reduced mechanical loading. Next, the effect of nonsteroidal anti-inflammatory drugs (NSAIDs) on the leukocyte composition revealed that, even though NSAIDs influence the mechanical properties of healing tendon, this effect was not mediated via changes in the leukocyte sub-populations during early and mid-time tendon healing. Further, the effect of corticosteroids during the inflammatory and remodeling phases of tendon healing was an improved healing of tendons and a reduction of CD8a T cells when corticosteroid was administered after the inflammatory phase. Lastly, we investigated if impairment of tendon healing by NSAIDs was related to mechanotransduction or microdamage during mechanical loading and showed that NSAIDs impair tendon healing by reducing the response to microdamage. In conclusion, these studies show that inflammation plays an important role during Achilles tendon healing, and factors that influence healing can also alter the presence or polarization of immune cell populations.

10

Eustace, Andrew David. "Syndecan 3 and inflammation." Thesis, University of Bristol, 2016. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.720843.

Full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Books on the topic "Inflammation":

1

Clausen, Björn E., and Jon D. Laman, eds. Inflammation. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6786-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Górski, Andrzej, Hubert Krotkiewski, and Michał Zimecki, eds. Inflammation. Dordrecht: Springer Netherlands, 2001. http://dx.doi.org/10.1007/978-94-015-9702-9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Pierangelo, Geppetti, and Holzer, Peter, Mag. rer. nat. Dr. phil., eds. Neurogenic inflammation. Boca Raton: CRC Press, 1996.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

4

Winyard, Paul G., and Derek A. Willoughby. Inflammation Protocols. New Jersey: Humana Press, 2003. http://dx.doi.org/10.1385/1592593747.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Miyasaka, Masayuki, and Kiyoshi Takatsu, eds. Chronic Inflammation. Tokyo: Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-56068-5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Zierhut, Manfred, Carlos Pavesio, Shigeaki Ohno, Fernando Orefice, and Narsing A. Rao, eds. Intraocular Inflammation. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-540-75387-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Man, Francis, and Simon J. Cleary, eds. Imaging Inflammation. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-23661-7.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Challem, Jack. The Inflammation Syndrome. New York: John Wiley & Sons, Ltd., 2003.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

9

Andreas, Bosio, and Gerstmayer Bernhard, eds. Microarrays in inflammation. Basel: Birkhäuser, 2008.

Find full text

APA, Harvard, Vancouver, ISO, and other styles

10

Rogers, Duncan F., and Louise E. Donnelly. Human Airway Inflammation. New Jersey: Humana Press, 2001. http://dx.doi.org/10.1385/1592591515.

Full text

APA, Harvard, Vancouver, ISO, and other styles

More sources

Book chapters on the topic "Inflammation":

1

Bährle-Rapp, Marina. "Inflammation, auch: Inflammatio." In Springer Lexikon Kosmetik und Körperpflege, 279. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_5191.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Citerio, G., C. Giussani, Hugo Sax, Didier Pittet, Xiaoyan Wen, John A. Kellum, Angela M. Mills, et al. "Inflammation." In Encyclopedia of Intensive Care Medicine, 1230. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-00418-6_3166.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Hayashi, Nariyuki, and Dalton W. Dietrich. "Inflammation." In Brain Hypothermia Treatment, 28–29. Tokyo: Springer Japan, 2004. http://dx.doi.org/10.1007/978-4-431-53953-7_18.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Elgazzar, Abdelhamid H., and Ismet Sarikaya. "Inflammation." In Nuclear Medicine Companion, 243–56. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-76156-5_9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Elgazzar, Abdelhamid H. "Inflammation." In Synopsis of Pathophysiology in Nuclear Medicine, 41–57. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-03458-4_4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Collins, Caitlin, Ellie Tzima, and Cam Patterson. "Inflammation." In Atherosclerosis, 43–52. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118828533.ch4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Neumann, Harald. "Inflammation." In Neuroprotection, 173–90. Weinheim, FRG: Wiley-VCH Verlag GmbH & Co. KGaA, 2005. http://dx.doi.org/10.1002/3527603867.ch9.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Johnson, Susan K. "Inflammation." In Encyclopedia of Clinical Neuropsychology, 1803–4. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-57111-9_561.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Santiago, Jonas Francisco Y. "Inflammation." In Positron Emission Tomography with Computed Tomography (PET/CT), 35–48. Cham: Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-05518-3_5.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Rohleder, Nicolas, and Jutta M. Wolf. "Inflammation." In Encyclopedia of Behavioral Medicine, 1187–89. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-39903-0_25.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Conference papers on the topic "Inflammation":

1

"Chronic Inflammation." In INTERNATIONAL CONFERENCE ON BIOLOGICAL RESEARCH AND APPLIED SCIENCE. Jinnah University for Women, 2024. http://dx.doi.org/10.37962/ibras/2024/105.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Wang, Dingzhi, Lixia Guo, Wei Ning, and Raymond N. DuBois. "Abstract A43: PPARδ promotes colonic inflammation and inflammation-associated tumorigenesis." In Abstracts: AACR International Conference on Frontiers in Cancer Prevention Research‐‐ Oct 22-25, 2011; Boston, MA. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1940-6207.prev-11-a43.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Kwon, Byungsuk, and Hong Rae Cho. "CD137 reverse signaling in sterile inflammation: CD137L in sterile tissue inflammation." In 2012 7th International Forum on Strategic Technology (IFOST). IEEE, 2012. http://dx.doi.org/10.1109/ifost.2012.6357821.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Kramer, Violet, Fan Chen, Daisuke Nonaka, and Angeliki Kazeros. "Paraneoplastic Pulmonary Eosinophilic Inflammation." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a3995.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Yousuf, Ahmed Javid, Gita Parekh, Sarah Parker, Sara Glover, Jo Finch, Liesl Carr, Vijay Mistry, et al. "EXACT-PRO correlates with FEV1 and systemic inflammation but not airway inflammation." In ERS International Congress 2019 abstracts. European Respiratory Society, 2019. http://dx.doi.org/10.1183/13993003.congress-2019.pa2692.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Visser, Tjaakje, Mirrin Dorresteijn, Anky Koenderman, Luke Leenen, Peter Pickkers, and Leo Koenderman. "Inhibition Of Acute Inflammation By C1-esteraseinhibitor In A Human Inflammation Model." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a6034.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Ford, M. L., B. W. Lewis, K. Heyob, T. Harshman, M. Guerau-De-Arellano, and R. D. Britt. "CD38 Promotes Th17 Inflammation in Aged Mice With Severe Allergic Airway Inflammation." In American Thoracic Society 2023 International Conference, May 19-24, 2023 - Washington, DC. American Thoracic Society, 2023. http://dx.doi.org/10.1164/ajrccm-conference.2023.207.1_meetingabstracts.a2810.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Machado, Luiza, Camila Santos, Bianca Leonardi, Andréia Rocha, Igor Fontana, Bruna Bellaver, Gianina Venturin, et al. "ACUTE PERIPHERAL INFLAMMATION IMPACT ON CEREBRAL GLUCOSE METABOLISM." In XIII Meeting of Researchers on Alzheimer's Disease and Related Disorders. Zeppelini Editorial e Comunicação, 2021. http://dx.doi.org/10.5327/1980-5764.rpda072.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Abstract:

Background: Neuroinflammation is a phenomenon already described in Alzheimer’s disease (AD). However, the effect of peripheral inflammation in AD is less understood. We recently demonstrated that severe sepsis causes acute brain metabolic disturbances. Nevertheless, whether mild acute peripheral inflammation affects brain metabolism remains unclear. Objective: We aimed at investigating the impact of mild acute peritonitis on glucose brain metabolism. Methods: Adult male wistar rats (n=6, per group) received a single intraperitoneal injection of 500 ml of carrageenan (CG, 500 µg of carrageenan i.p.) or saline (CO). Brain glucose metabolism was assessed using (18F) FDG-PET 4h after i.p. injections, which represents the first peak of inflammation. The peripheral inflammatory process was evaluated by analyzing the peritoneal lavage in a flow cytometer 48h after the injections, during the second peak of inflammation. Results: The CG animals presented a 5-fold increase in macrophages numbers (p0,05). However, carrageenan-induced inflammation did not cause acute changes in brain glucose metabolism (p>0,05). Conclusion: Mild acute peripheral inflammation does not change brain glucose metabolism. Further evaluations aiming to investigate long-term consequences of sustained mild inflammation are needed.

9

Wang, Dingzhi, Lixia Guo, Wei Ning, Hong Wu, Rupesh Chaturved, Keith Wilson, and Raymond N. DuBois. "Abstract 1519: Peroxisome proliferator-activated receptor ≤ promotes colonic inflammation and inflammation-associated tumorigenesis." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-1519.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Latorre, Manuela, Chiara Baldini, Federica Novelli, Federico Dente, S. Grosso, P. Della Rossa, Silvana Cianchetti, Stefano Bombardieri, and Pierluigi Paggiaro. "Airway Inflammation And Systemic Inflammation In Churg-Strauss Syndrome: Two Faces Of Disease." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a4207.

Full text

APA, Harvard, Vancouver, ISO, and other styles

Reports on the topic "Inflammation":

1

Krueger, Lucas A., Donald C. Beitz, Robert L. Stuart, and Judith R. Stabel. Early Inflammation Disorder in Neonatal Calves. Ames (Iowa): Iowa State University, January 2015. http://dx.doi.org/10.31274/ans_air-180814-1290.

Full text

APA, Harvard, Vancouver, ISO, and other styles

2

Bach, Ronald R. Gulf War Illness Inflammation Reduction Trial. Fort Belvoir, VA: Defense Technical Information Center, October 2015. http://dx.doi.org/10.21236/ada626080.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Beal, M. F. Bioenergetic Approaches and Inflammation in MPTP Toxicity. Fort Belvoir, VA: Defense Technical Information Center, September 2005. http://dx.doi.org/10.21236/ada439263.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Jerde, Travis J. Phosphoinositide-Driven Epithelial Proliferation in Prostatic Inflammation. Fort Belvoir, VA: Defense Technical Information Center, January 2008. http://dx.doi.org/10.21236/ada485294.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Beal, M. F. Bioenergetic Approaches and inflammation of MPTP Toxicity. Fort Belvoir, VA: Defense Technical Information Center, September 2008. http://dx.doi.org/10.21236/ada488708.

Full text

APA, Harvard, Vancouver, ISO, and other styles

6

Beal, M. F. Bioenergetic Approaches and Inflammation of MPTP Toxicity. Fort Belvoir, VA: Defense Technical Information Center, September 2009. http://dx.doi.org/10.21236/ada508622.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Jerde, Travis J., and Wade Bushman. Phosphoinositide-Driven Epithelial Proliferation in Prostatic Inflammation. Fort Belvoir, VA: Defense Technical Information Center, April 2009. http://dx.doi.org/10.21236/ada510023.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Durbin, Megan C. The Effects of Exercise on Brain Inflammation. Fort Belvoir, VA: Defense Technical Information Center, June 2010. http://dx.doi.org/10.21236/ada524163.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Broaddus, V. C. Role of Macrophage-induced Inflammation in Mesothelioma. Fort Belvoir, VA: Defense Technical Information Center, July 2012. http://dx.doi.org/10.21236/ada582550.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Beal, M. F. Bioenergetic Approaches and Inflammation of MPTP Toxicity. Fort Belvoir, VA: Defense Technical Information Center, September 2007. http://dx.doi.org/10.21236/ada482978.

Full text

APA, Harvard, Vancouver, ISO, and other styles