Skip to main content
Erschienen in: Inflammation 6/2022

05.07.2022 | Original Article

Gallic Acid Improves Therapeutic Effects of Mesenchymal Stem Cells Derived from Adipose Tissue in Acute Renal Injury Following Rhabdomyolysis Induced by Glycerol

verfasst von: Seyyed Ali Mard, Khojasteh Hoseinynejad, Fereshteh Nejaddehbashi

Erschienen in: Inflammation | Ausgabe 6/2022

Einloggen, um Zugang zu erhalten

Abstract

Acute kidney injury (AKI) is identified by a progressive reduction in the glomerular filtration rate (GFR) and retention of nitrogenous waste products. Traumatic and nontraumatic rhabdomyolysis is recently considered the main cause of AKI. According to several studies, stem cell treatment is a promising therapeutic strategy for many types of disorders including AKI. The main limitation of mesenchymal stem cells (MSCs) therapy is reducing cell survival in response to oxidative stress products in injured organ areas. Gallic acid (GA) as a well-known antioxidant has been reported to confer potent-free radical scavenging and anti-inflammatory properties. Therefore, the aim of the current study was to assess the influence of MSCs and GA in acute renal injury following rhabdomyolysis induced by glycerol. A total of 70 healthy rats were divided into seven groups (10 in each group): control, AKI (glycerol, intramuscular), cell therapy (AKI + intravenous injection of mesenchymal stem cells derived from adipose tissue (AMCs), AKI + AMCs + GA (50, 100, and 200 mg/kg, intraperitoneally, 3 days a week for 3 consecutive weeks), and positive control group (the most effective dose of gallic acid). After the treatment, rats were sacrificed; blood, urine, and kidney tissues were collected; and qualitative and quantitative parameters (including blood urea nitrogen (BUN), creatine kinase (CK), lactate dehydrogenase (LDH), alkaline phosphatase (ALP), aspartate transaminase (SGOT), oxidative stress markers kidney function parameters) and histopathological indexes were assayed. Our results revealed that co-treatment of AMCs plus GA into AKI rats decreased BUN and creatinine and ameliorated kidney injury parameters after 3 weeks. Improved oxidative stress markers such as decreased MDA and increased SOD and CAT were significant in the GA + AMCs group compared to the AMCs alone in AKI rats. Also, the histopathological appearances of AKI rats including renal tubule cavity expansion and renal tubular epithelial cell edema, and interstitial inflammation, were alleviated using GA + AMCs treatment compared to the control. The obtained results of the current study documented that antioxidants could make mesenchymal stem cells more resistant to the condition in which they are supposed to be transplanted and probably improve the efficacy of stem cell therapy in AKI patients.
Literatur
1.
Zurück zum Zitat Makris, K., and L. Spanou. 2016. Acute kidney injury: Definition, pathophysiology and clinical phenotypes. The clinical biochemist reviews. 37 (2): 85.PubMedPubMedCentral Makris, K., and L. Spanou. 2016. Acute kidney injury: Definition, pathophysiology and clinical phenotypes. The clinical biochemist reviews. 37 (2): 85.PubMedPubMedCentral
2.
Zurück zum Zitat Kellum, J.A., and N. Lameire. 2013. Diagnosis, evaluation, and management of acute kidney injury: A KDIGO summary (part 1). Critical care. 17 (1): 1–5.CrossRef Kellum, J.A., and N. Lameire. 2013. Diagnosis, evaluation, and management of acute kidney injury: A KDIGO summary (part 1). Critical care. 17 (1): 1–5.CrossRef
3.
Zurück zum Zitat Nishimura, H., H. Enokida, S. Kawahira, I. Kagara, H. Hayami, and M. Nakagawa. 2016. Acute kidney injury and rhabdomyolysis after Protobothrops flavoviridis bite: A retrospective survey of 86 patients in a tertiary care center. The American journal of tropical medicine and hygiene. 94 (2): 474–479.CrossRefPubMedPubMedCentral Nishimura, H., H. Enokida, S. Kawahira, I. Kagara, H. Hayami, and M. Nakagawa. 2016. Acute kidney injury and rhabdomyolysis after Protobothrops flavoviridis bite: A retrospective survey of 86 patients in a tertiary care center. The American journal of tropical medicine and hygiene. 94 (2): 474–479.CrossRefPubMedPubMedCentral
4.
Zurück zum Zitat Keltz, E., F.Y. Khan, and G. Mann. 2013. Rhabdomyolysis. The role of diagnostic and prognostic factors. Muscles, ligaments and tendons journal. 3 (4): 303. Keltz, E., F.Y. Khan, and G. Mann. 2013. Rhabdomyolysis. The role of diagnostic and prognostic factors. Muscles, ligaments and tendons journal. 3 (4): 303.
5.
Zurück zum Zitat Emzhik, M., P. Makhdoumi, N. Milani, and B. Dadpour. 2019. Role of acetaminophen in reducing risk of kidney injury from rhabdomyolysis: A narrative review. Asia Pacific Journal of Medical Toxicology. 8 (2): 61–64. Emzhik, M., P. Makhdoumi, N. Milani, and B. Dadpour. 2019. Role of acetaminophen in reducing risk of kidney injury from rhabdomyolysis: A narrative review. Asia Pacific Journal of Medical Toxicology. 8 (2): 61–64.
6.
Zurück zum Zitat Zhou, X.J., Z. Laszik, X.Q. Wang, F.G. Silva, and N.D. Vaziri. 2000. Association of renal injury with increased oxygen free radical activity and altered nitric oxide metabolism in chronic experimental hemosiderosis. Laboratory investigation. 80 (12): 1905–1914.CrossRefPubMed Zhou, X.J., Z. Laszik, X.Q. Wang, F.G. Silva, and N.D. Vaziri. 2000. Association of renal injury with increased oxygen free radical activity and altered nitric oxide metabolism in chronic experimental hemosiderosis. Laboratory investigation. 80 (12): 1905–1914.CrossRefPubMed
7.
Zurück zum Zitat Plotnikov, E.Y., A.A. Chupyrkina, I.B. Pevzner, N.K. Isaev, and D.B. Zorov. 2009. Myoglobin causes oxidative stress, increase of NO production and dysfunction of kidney’s mitochondria. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease. 1792 (8): 796–803. Plotnikov, E.Y., A.A. Chupyrkina, I.B. Pevzner, N.K. Isaev, and D.B. Zorov. 2009. Myoglobin causes oxidative stress, increase of NO production and dysfunction of kidney’s mitochondria. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease. 1792 (8): 796–803.
8.
Zurück zum Zitat Needham, E. 2005. Management of acute renal failure. American family physician. 72 (9): 1739–1746.PubMed Needham, E. 2005. Management of acute renal failure. American family physician. 72 (9): 1739–1746.PubMed
9.
Zurück zum Zitat Chatzizisis, Y.S., G. Misirli, A.I. Hatzitolios, and G.D. Giannoglou. 2008. The syndrome of rhabdomyolysis: Complications and treatment. European journal of internal medicine. 19 (8): 568–574.CrossRefPubMed Chatzizisis, Y.S., G. Misirli, A.I. Hatzitolios, and G.D. Giannoglou. 2008. The syndrome of rhabdomyolysis: Complications and treatment. European journal of internal medicine. 19 (8): 568–574.CrossRefPubMed
10.
Zurück zum Zitat Weiss, J.N., Z. Qu, and K. Shivkumar. 2017. Electrophysiology of hypokalemia and hyperkalemia. Circulation: Arrhythmia and Electrophysiology. 10 (3): e004667. Weiss, J.N., Z. Qu, and K. Shivkumar. 2017. Electrophysiology of hypokalemia and hyperkalemia. Circulation: Arrhythmia and Electrophysiology. 10 (3): e004667.
11.
Zurück zum Zitat Korrapati, M.C., B.E. Shaner, and R.G. Schnellmann. 2012. Recovery from glycerol-induced acute kidney injury is accelerated by suramin. Journal of Pharmacology and Experimental Therapeutics. 341 (1): 126–136.CrossRefPubMedPubMedCentral Korrapati, M.C., B.E. Shaner, and R.G. Schnellmann. 2012. Recovery from glycerol-induced acute kidney injury is accelerated by suramin. Journal of Pharmacology and Experimental Therapeutics. 341 (1): 126–136.CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Gyurászová, M., A.G. Kovalčíková, E. Renczés, K. Kmeťová, P. Celec, J. Bábíčková, and Ľ Tóthová. 2019. Oxidative stress in animal models of acute and chronic renal failure. Disease markers. 11: 2019. Gyurászová, M., A.G. Kovalčíková, E. Renczés, K. Kmeťová, P. Celec, J. Bábíčková, and Ľ Tóthová. 2019. Oxidative stress in animal models of acute and chronic renal failure. Disease markers. 11: 2019.
13.
Zurück zum Zitat Mousleh, R., S. Al Laham, and A. Al-Manadili. 2018. The preventive role of pioglitazone in glycerol-induced acute kidney injury in rats during two different treatment periods. Iranian journal of medical sciences. 43 (2): 184.PubMedPubMedCentral Mousleh, R., S. Al Laham, and A. Al-Manadili. 2018. The preventive role of pioglitazone in glycerol-induced acute kidney injury in rats during two different treatment periods. Iranian journal of medical sciences. 43 (2): 184.PubMedPubMedCentral
14.
Zurück zum Zitat Zurovsky, Y. 1993. Models of glycerol-induced acute renal failure in rats. Journal of Basic and Clinical Physiology and Pharmacology. 4 (3): 213–228.CrossRefPubMed Zurovsky, Y. 1993. Models of glycerol-induced acute renal failure in rats. Journal of Basic and Clinical Physiology and Pharmacology. 4 (3): 213–228.CrossRefPubMed
15.
Zurück zum Zitat Panizo, N., A. Rubio-Navarro, J.M. Amaro-Villalobos, J. Egido, and J.A. Moreno. 2015. Molecular mechanisms and novel therapeutic approaches to rhabdomyolysis-induced acute kidney injury. Kidney and Blood Pressure Research. 40 (5): 520–532.CrossRefPubMed Panizo, N., A. Rubio-Navarro, J.M. Amaro-Villalobos, J. Egido, and J.A. Moreno. 2015. Molecular mechanisms and novel therapeutic approaches to rhabdomyolysis-induced acute kidney injury. Kidney and Blood Pressure Research. 40 (5): 520–532.CrossRefPubMed
16.
Zurück zum Zitat Ullah, I., R.B. Subbarao, and G.J. Rho. 2015. Human mesenchymal stem cells-current trends and future prospective. Bioscience reports. 35 (2). Ullah, I., R.B. Subbarao, and G.J. Rho. 2015. Human mesenchymal stem cells-current trends and future prospective. Bioscience reports. 35 (2).
17.
Zurück zum Zitat Berebichez-Fridman, R., and P.R. Montero-Olvera. 2018. Sources and clinical applications of mesenchymal stem cells: State-of-the-art review. Sultan Qaboos University Medical Journal. 18 (3): e264.CrossRefPubMedPubMedCentral Berebichez-Fridman, R., and P.R. Montero-Olvera. 2018. Sources and clinical applications of mesenchymal stem cells: State-of-the-art review. Sultan Qaboos University Medical Journal. 18 (3): e264.CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat Joyce, N., G. Annett, L. Wirthlin, S. Olson, G. Bauer, and J.A. Nolta. 2010. Mesenchymal stem cells for the treatment of neurodegenerative disease. Regenerative medicine. 5 (6): 933–946.CrossRefPubMed Joyce, N., G. Annett, L. Wirthlin, S. Olson, G. Bauer, and J.A. Nolta. 2010. Mesenchymal stem cells for the treatment of neurodegenerative disease. Regenerative medicine. 5 (6): 933–946.CrossRefPubMed
19.
Zurück zum Zitat Hosseini, A., F. Amiri, F. Khalighi, A.M. Roushandeh, Y. Kuwahara, H. Bashiri, and M.H. Roudkenar. 2019. Cell survival effects of autophagy regulation on umbilical cord-derived mesenchymal stem cells following exposure to oxidative stress. Iranian journal of medical sciences. 44 (6): 493.PubMed Hosseini, A., F. Amiri, F. Khalighi, A.M. Roushandeh, Y. Kuwahara, H. Bashiri, and M.H. Roudkenar. 2019. Cell survival effects of autophagy regulation on umbilical cord-derived mesenchymal stem cells following exposure to oxidative stress. Iranian journal of medical sciences. 44 (6): 493.PubMed
20.
Zurück zum Zitat Pandey, K.B., and S.I. Rizvi. 2009. Plant polyphenols as dietary antioxidants in human health and disease. Oxidative medicine and cellular longevity. 2 (5): 270–278.CrossRefPubMedPubMedCentral Pandey, K.B., and S.I. Rizvi. 2009. Plant polyphenols as dietary antioxidants in human health and disease. Oxidative medicine and cellular longevity. 2 (5): 270–278.CrossRefPubMedPubMedCentral
21.
Zurück zum Zitat Shaban, S., M.W. El-Husseny, A.I. Abushouk, A.M. Salem, M. Mamdouh, and M.M. Abdel-Daim. 2017. Effects of antioxidant supplements on the survival and differentiation of stem cells. Oxidative Medicine and Cellular Longevity. 1: 2017. Shaban, S., M.W. El-Husseny, A.I. Abushouk, A.M. Salem, M. Mamdouh, and M.M. Abdel-Daim. 2017. Effects of antioxidant supplements on the survival and differentiation of stem cells. Oxidative Medicine and Cellular Longevity. 1: 2017.
22.
Zurück zum Zitat Fernandes, F.H., and H.R. Salgado. 2016. Gallic acid: Review of the methods of determination and quantification. Critical reviews in analytical chemistry. 46 (3): 257–265.CrossRefPubMed Fernandes, F.H., and H.R. Salgado. 2016. Gallic acid: Review of the methods of determination and quantification. Critical reviews in analytical chemistry. 46 (3): 257–265.CrossRefPubMed
23.
Zurück zum Zitat Kahkeshani, N., F. Farzaei, M. Fotouhi, S.S. Alavi, R. Bahramsoltani, R. Naseri, S. Momtaz, Z. Abbasabadi, R. Rahimi, M.H. Farzaei, and A. Bishayee. 2019. Pharmacological effects of gallic acid in health and diseases: A mechanistic review. Iranian journal of basic medical sciences. 22 (3): 225.PubMedPubMedCentral Kahkeshani, N., F. Farzaei, M. Fotouhi, S.S. Alavi, R. Bahramsoltani, R. Naseri, S. Momtaz, Z. Abbasabadi, R. Rahimi, M.H. Farzaei, and A. Bishayee. 2019. Pharmacological effects of gallic acid in health and diseases: A mechanistic review. Iranian journal of basic medical sciences. 22 (3): 225.PubMedPubMedCentral
24.
Zurück zum Zitat Ajibade, T.O., A.A. Oyagbemi, T.O. Omobowale, E.R. Asenuga, J.M. Afolabi, and A.A. Adedapo. 2016. Mitigation of diazinon-induced cardiovascular and renal dysfunction by gallic acid. Interdisciplinary toxicology. 9 (2): 66–77.CrossRefPubMed Ajibade, T.O., A.A. Oyagbemi, T.O. Omobowale, E.R. Asenuga, J.M. Afolabi, and A.A. Adedapo. 2016. Mitigation of diazinon-induced cardiovascular and renal dysfunction by gallic acid. Interdisciplinary toxicology. 9 (2): 66–77.CrossRefPubMed
25.
Zurück zum Zitat Zhang, J.B., X.Q. Wang, G.L. Lu, H.S. Huang, and S.Y. Xu. 2017. Adipose-derived mesenchymal stem cells therapy for acute kidney injury induced by ischemia-reperfusion in a rat model. Clinical and Experimental Pharmacology and Physiology. 44 (12): 1232–1240.CrossRefPubMed Zhang, J.B., X.Q. Wang, G.L. Lu, H.S. Huang, and S.Y. Xu. 2017. Adipose-derived mesenchymal stem cells therapy for acute kidney injury induced by ischemia-reperfusion in a rat model. Clinical and Experimental Pharmacology and Physiology. 44 (12): 1232–1240.CrossRefPubMed
26.
Zurück zum Zitat Canbek, M., G. Bayramoglu, H. Senturk, A.V. Oztopcu, M. Uyanoglu, E. Ceyhan, A. Ozen, B. Durmus, K. Kartkaya, and G. Kanbak. 2014. The examination of protective effects of gallic acid against damage of oxidative stress during induced-experimental renal ischemia-reperfusion in experiment. Bratislavske lekarske listy. 115 (9): 557–562.PubMed Canbek, M., G. Bayramoglu, H. Senturk, A.V. Oztopcu, M. Uyanoglu, E. Ceyhan, A. Ozen, B. Durmus, K. Kartkaya, and G. Kanbak. 2014. The examination of protective effects of gallic acid against damage of oxidative stress during induced-experimental renal ischemia-reperfusion in experiment. Bratislavske lekarske listy. 115 (9): 557–562.PubMed
27.
Zurück zum Zitat Zhao, W., X. Huang, L. Zhang, X. Yang, L. Wang, Y. Chen, J. Wang, and G. Wu. 2016. Penehyclidine hydrochloride pretreatment ameliorates rhabdomyolysis-induced AKI by activating the Nrf2/HO-1 pathway and allevi-ating endoplasmic reticulum stress in rats. PLoS ONE 11 (3): e0151158.CrossRefPubMedPubMedCentral Zhao, W., X. Huang, L. Zhang, X. Yang, L. Wang, Y. Chen, J. Wang, and G. Wu. 2016. Penehyclidine hydrochloride pretreatment ameliorates rhabdomyolysis-induced AKI by activating the Nrf2/HO-1 pathway and allevi-ating endoplasmic reticulum stress in rats. PLoS ONE 11 (3): e0151158.CrossRefPubMedPubMedCentral
28.
Zurück zum Zitat Ward, M.M. 1988. Factors predictive of acute renal failure in rhabdomyolysis. Archives of internal medicine. 148 (7): 1553–1557.CrossRefPubMed Ward, M.M. 1988. Factors predictive of acute renal failure in rhabdomyolysis. Archives of internal medicine. 148 (7): 1553–1557.CrossRefPubMed
29.
Zurück zum Zitat Cervellin, G., I. Comelli, M. Benatti, F. Sanchis-Gomar, and G. Lippi. 2017. Nontraumatic rhabdomyolysis: background, laboratory features, and acute clinical management. Clinical Biochemistry. 50 (12): 656-62. Cervellin, G., I. Comelli, M. Benatti, F. Sanchis-Gomar,  and G. Lippi. 2017. Nontraumatic rhabdomyolysis: background, laboratory features, and acute clinical management. Clinical Biochemistry. 50 (12): 656-62.
30.
Zurück zum Zitat Selim, R.E., H.H. Ahmed, S.H. Abd-Allah, G.M. Sabry, R.E. Hassan, W.K. Khalil, and N.S. Abouhashem. 2019. Mesenchymal stem cells: A promising therapeutic tool for acute kidney injury. Applied biochemistry and biotechnology. 189 (1): 284–304.CrossRefPubMed Selim, R.E., H.H. Ahmed, S.H. Abd-Allah, G.M. Sabry, R.E. Hassan, W.K. Khalil, and N.S. Abouhashem. 2019. Mesenchymal stem cells: A promising therapeutic tool for acute kidney injury. Applied biochemistry and biotechnology. 189 (1): 284–304.CrossRefPubMed
32.
Zurück zum Zitat Zhao, L., F. Han, J. Wang, and J. Chen. 2019. Current understanding of the administration of mesenchymal stem cells in acute kidney injury to chronic kidney disease transition: A review with a focus on preclinical models. Stem cell research & therapy. 10 (1): 1–1.CrossRef Zhao, L., F. Han, J. Wang, and J. Chen. 2019. Current understanding of the administration of mesenchymal stem cells in acute kidney injury to chronic kidney disease transition: A review with a focus on preclinical models. Stem cell research & therapy. 10 (1): 1–1.CrossRef
33.
Zurück zum Zitat Baldari, S., G. Di Rocco, M. Piccoli, M. Pozzobon, M. Muraca, and G. Toietta. 2017. Challenges and strategies for improving the regenerative effects of mesenchymal stromal cell-based therapies. International journal of molecular sciences. 18 (10): 2087.CrossRefPubMedCentral Baldari, S., G. Di Rocco, M. Piccoli, M. Pozzobon, M. Muraca, and G. Toietta. 2017. Challenges and strategies for improving the regenerative effects of mesenchymal stromal cell-based therapies. International journal of molecular sciences. 18 (10): 2087.CrossRefPubMedCentral
34.
Zurück zum Zitat Cho, Y.S., S.K. Kim, C.B. Ahn, and J.Y. Je. 2011. Preparation, characterization, and antioxidant properties of gallic acid-grafted-chitosans. Carbohydrate Polymers. 83 (4): 1617–1622.CrossRef Cho, Y.S., S.K. Kim, C.B. Ahn, and J.Y. Je. 2011. Preparation, characterization, and antioxidant properties of gallic acid-grafted-chitosans. Carbohydrate Polymers. 83 (4): 1617–1622.CrossRef
35.
Zurück zum Zitat Oboh, G., M.D. Ogunbadejo, O.B. Ogunsuyi, and S.I. Oyeleye. 2020. Can gallic acid potentiate the antihyperglycemic effect of acarbose and metformin? Evidence from streptozotocin-induced diabetic rat model. Archives of Physiology and Biochemistry. 23: 1–9. Oboh, G., M.D. Ogunbadejo, O.B. Ogunsuyi, and S.I. Oyeleye. 2020. Can gallic acid potentiate the antihyperglycemic effect of acarbose and metformin? Evidence from streptozotocin-induced diabetic rat model. Archives of Physiology and Biochemistry. 23: 1–9.
36.
Zurück zum Zitat Kroes, B.V., A.J. Van den Berg, H.Q. Van Ufford, H. Van Dijk, and R.P. Labadie. 1992. Anti-inflammatory activity of gallic acid. Planta medica. 58 (06): 499–504.CrossRefPubMed Kroes, B.V., A.J. Van den Berg, H.Q. Van Ufford, H. Van Dijk, and R.P. Labadie. 1992. Anti-inflammatory activity of gallic acid. Planta medica. 58 (06): 499–504.CrossRefPubMed
37.
Zurück zum Zitat Mohammadzadeh-Vardin, M., M.H. Roudkenar, and A. Jahanian-Najafabadi. 2015. Adenovirus-mediated over-expression of Nrf2 within mesenchymal stem cells (MSCs) protected rats against acute kidney injury. Advanced pharmaceutical bulletin. 5 (2): 201.CrossRefPubMedPubMedCentral Mohammadzadeh-Vardin, M., M.H. Roudkenar, and A. Jahanian-Najafabadi. 2015. Adenovirus-mediated over-expression of Nrf2 within mesenchymal stem cells (MSCs) protected rats against acute kidney injury. Advanced pharmaceutical bulletin. 5 (2): 201.CrossRefPubMedPubMedCentral
38.
Zurück zum Zitat Liu, N., G. Han, J. Cheng, J. Huang, and J. Tian. 2013. Erythropoietin promotes the repair effect of acute kidney injury by bone-marrow mesenchymal stem cells transplantation. Experimental biology and medicine. 238 (6): 678–686.CrossRefPubMed Liu, N., G. Han, J. Cheng, J. Huang, and J. Tian. 2013. Erythropoietin promotes the repair effect of acute kidney injury by bone-marrow mesenchymal stem cells transplantation. Experimental biology and medicine. 238 (6): 678–686.CrossRefPubMed
39.
Zurück zum Zitat Masoud, M.S., S.S. Anwar, M.Z. Afzal, A. Mehmood, S.N. Khan, and S. Riazuddin. 2012. Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment. Journal of Translational Medicine. 10 (1): 1–1.CrossRef Masoud, M.S., S.S. Anwar, M.Z. Afzal, A. Mehmood, S.N. Khan, and S. Riazuddin. 2012. Pre-conditioned mesenchymal stem cells ameliorate renal ischemic injury in rats by augmented survival and engraftment. Journal of Translational Medicine. 10 (1): 1–1.CrossRef
Metadaten
Titel
Gallic Acid Improves Therapeutic Effects of Mesenchymal Stem Cells Derived from Adipose Tissue in Acute Renal Injury Following Rhabdomyolysis Induced by Glycerol
verfasst von
Seyyed Ali Mard
Khojasteh Hoseinynejad
Fereshteh Nejaddehbashi
Publikationsdatum
05.07.2022
Verlag
Springer US
Erschienen in
Inflammation / Ausgabe 6/2022
Print ISSN: 0360-3997
Elektronische ISSN: 1573-2576
DOI
https://doi.org/10.1007/s10753-022-01691-4

Weitere Artikel der Ausgabe 6/2022

Inflammation 6/2022 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Bei seelischem Stress sind Checkpoint-Hemmer weniger wirksam

03.06.2024 NSCLC Nachrichten

Wie stark Menschen mit fortgeschrittenem NSCLC von einer Therapie mit Immun-Checkpoint-Hemmern profitieren, hängt offenbar auch davon ab, wie sehr die Diagnose ihre psychische Verfassung erschüttert

Antikörper mobilisiert Neutrophile gegen Krebs

03.06.2024 Onkologische Immuntherapie Nachrichten

Ein bispezifischer Antikörper formiert gezielt eine Armee neutrophiler Granulozyten gegen Krebszellen. An den Antikörper gekoppeltes TNF-alpha soll die Zellen zudem tief in solide Tumoren hineinführen.

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

Nach Herzinfarkt mit Typ-1-Diabetes schlechtere Karten als mit Typ 2?

29.05.2024 Herzinfarkt Nachrichten

Bei Menschen mit Typ-2-Diabetes sind die Chancen, einen Myokardinfarkt zu überleben, in den letzten 15 Jahren deutlich gestiegen – nicht jedoch bei Betroffenen mit Typ 1.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.