Academic Journal
β-carotene attenuates calcium oxalate crystal-induced renal injury through suppression of NF-κB-mediated inflammation.
| Title: | β-carotene attenuates calcium oxalate crystal-induced renal injury through suppression of NF-κB-mediated inflammation. |
|---|---|
| Authors: | Su M; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China. Smq93885@163.com., Guan Y; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China., Wei H; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China., Chen L; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China., Dong W; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China. |
| Source: | Urolithiasis [Urolithiasis] 2026 Sep 12; Vol. 54 (1). Date of Electronic Publication: 2026 Sep 12. |
| Publication Type: | Journal Article |
| Language: | English |
| Journal Info: | Publisher: Springer Country of Publication: Germany NLM ID: 101602699 Publication Model: Electronic Cited Medium: Internet ISSN: 2194-7236 (Electronic) Linking ISSN: 21947228 NLM ISO Abbreviation: Urolithiasis Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: Berlin : Springer, [2013]- |
| MeSH Terms: | beta Carotene*/pharmacology , beta Carotene*/therapeutic use , NF-kappa B*/metabolism , NF-kappa B*/antagonists & inhibitors , Calcium Oxalate*/chemistry , Inflammation*/drug therapy , Nephrocalcinosis*/chemically induced , Nephrocalcinosis*/drug therapy , Nephrocalcinosis*/pathology , Nephrolithiasis*/drug therapy, Signal Transduction/drug effects ; Signal Transduction/immunology ; Kidney Tubules, Proximal/cytology ; Kidney Tubules, Proximal/drug effects ; Kidney/pathology ; Kidney/drug effects ; Animals ; Mice ; Humans ; Disease Models, Animal ; Male ; Cell Line ; Molecular Docking Simulation |
| Abstract: | Calcium oxalate (CaOx) nephrolithiasis represents the most prevalent form of kidney stone disease and is characterized by persistent renal inflammation and tissue damage. β-Carotene, a naturally occurring carotenoid with well-documented anti-inflammatory properties, has demonstrated beneficial effects in a variety of inflammatory conditions; however, its potential role in CaOx crystal-associated renal injury remains largely unexplored. In this study, the effects of β-carotene on CaOx-induced renal damage were evaluated using both cellular and animal models. In human renal proximal tubular epithelial (HK-2) cells, β-carotene effectively alleviated calcium oxalate monohydrate (COM)-induced injury, decreased kidney injury molecule-1 (KIM-1) expression, and reduced the production of pro-inflammatory mediators, including TNF-α, IL-1β, IL-6, and MCP-1. Similarly, in a glyoxylate-induced nephrocalcinosis mouse model, β-carotene attenuated CaOx crystal accumulation, improved renal histopathological alterations and functional impairment, and suppressed inflammatory responses. To investigate the underlying mechanisms, network pharmacology and molecular docking analyses were conducted. A total of 145 overlapping targets were identified, and enrichment analyses identified NF-κB signaling as one of the candidate pathways potentially involved in the protective effects of β-carotene. Molecular docking analysis suggested favorable binding affinities between β-carotene and several key targets. Experimental validation demonstrated that β-carotene markedly inhibited NF-κB activation in both in vitro and in vivo settings, whereas pharmacological activation of NF-κB partially abolished its beneficial effects. Taken together, these findings indicate that β-carotene ameliorates CaOx crystal-induced renal injury and inflammation, at least in part through suppression of NF-κB signaling, and may offer a potential basis for the development of novel preventive and therapeutic approaches for kidney stone disease. (© 2026. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) |
| Competing Interests: | Declarations. Competing interests: The authors declare no competing interests. |
| References: | J Urol. 2005 Mar;173(3):848-57. (PMID: 15711292) Int J Urol. 2008 Feb;15(2):115-20. (PMID: 18269444) Cell Mol Life Sci. 2023 Sep 23;80(10):301. (PMID: 37740796) Nat Rev Nephrol. 2021 Jun;17(6):417-433. (PMID: 33514941) Eur J Med Res. 2025 Dec 10;30(1):1224. (PMID: 41372793) Phytomedicine. 2025 Jan;136:156302. (PMID: 39662099) J Nephrol. 2017 Apr;30(2):227-233. (PMID: 26969574) Int Urol Nephrol. 2024 Feb;56(2):423-431. (PMID: 37740155) Theranostics. 2020 Jun 5;10(16):7319-7334. (PMID: 32641994) Int Immunopharmacol. 2022 Jun;107:108677. (PMID: 35255299) Curr Drug Targets. 2025;26(9):591-612. (PMID: 40353475) J Urol. 2013 Mar;189(3):803-11. (PMID: 23022011) Front Pharmacol. 2022 Nov 03;13:1041117. (PMID: 36408256) J Am Soc Nephrol. 2009 Oct;20(10):2253-9. (PMID: 19679672) Arch Biochem Biophys. 2018 Aug 15;652:18-26. (PMID: 29885291) EBioMedicine. 2019 Dec;50:366-378. (PMID: 31735555) Pak J Biol Sci. 2009 Aug 15;12(16):1140-5. (PMID: 19899325) Food Funct. 2024 Dec 9;15(24):12033-12046. (PMID: 39563640) Int J Biol Sci. 2025 Apr 22;21(7):3099-3121. (PMID: 40384863) Int J Urol. 2008 Oct;15(10):924-8. (PMID: 18721209) Rev Urol. 2010 Spring;12(2-3):e86-96. (PMID: 20811557) J Food Sci. 2023 Jan;88(1):491-502. (PMID: 36448622) Chin J Nat Med. 2023 May;21(5):323-332. (PMID: 37245871) J Agric Food Chem. 2025 Jan 15;73(2):1542-1562. (PMID: 39741421) World J Urol. 2017 Sep;35(9):1301-1320. (PMID: 28213860) PLoS One. 2023 Apr 5;18(4):e0283779. (PMID: 37018237) Chem Biol Interact. 2017 Dec 25;278:114-122. (PMID: 29054323) Urolithiasis. 2025 Jul 2;53(1):134. (PMID: 40601009) Adv Sci (Weinh). 2026 Aug;13(43):e75585. (PMID: 42107057) Adv Chronic Kidney Dis. 2015 Jul;22(4):266-72. (PMID: 26088070) J Am Soc Nephrol. 2017 Mar;28(3):761-768. (PMID: 27612997) Adv Urol. 2018 Feb 4;2018:3068365. (PMID: 29515627) Transl Androl Urol. 2014 Sep;3(3):285-95. (PMID: 26816779) J Urol. 2022 Jan;207(1):144-151. (PMID: 34428923) J Food Sci. 2021 May;86(5):2118-2130. (PMID: 33884622) J Urol. 2010 Sep;184(3):1189-96. (PMID: 20663521) Phytomedicine. 2024 Dec;135:156145. (PMID: 39461201) Nat Rev Dis Primers. 2016 Feb 25;2:16008. (PMID: 27188687) Nutr Res. 2014 Nov;34(11):907-29. (PMID: 25134454) |
| Contributed Indexing: | Keywords: Kidney stones; Network pharmacology NF-κΒ; β-Carotene |
| Substance Nomenclature: | 01YAE03M7J (beta Carotene) 0 (NF-kappa B) 2612HC57YE (Calcium Oxalate) |
| Entry Date(s): | Date Created: 20260912 Date Completed: 20260912 Latest Revision: 20261008 |
| Update Code: | 20261008 |
| DOI: | 10.1007/s00240-026-02053-7 |
| PMID: | 42730918 |
| Database: | MEDLINE |
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| Items | – Name: Title Label: Title Group: Ti Data: β-carotene attenuates calcium oxalate crystal-induced renal injury through suppression of NF-κB-mediated inflammation. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Su+M%22">Su M</searchLink>; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China. Smq93885@163.com.<br /><searchLink fieldCode="AU" term="%22Guan+Y%22">Guan Y</searchLink>; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China.<br /><searchLink fieldCode="AU" term="%22Wei+H%22">Wei H</searchLink>; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China.<br /><searchLink fieldCode="AU" term="%22Chen+L%22">Chen L</searchLink>; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China.<br /><searchLink fieldCode="AU" term="%22Dong+W%22">Dong W</searchLink>; Department of Pathology, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University, Guangde Street, Yaohai District, Hefei City, Anhui Province, China. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101602699%22">Urolithiasis</searchLink> [Urolithiasis] 2026 Sep 12; Vol. 54 (1). <i>Date of Electronic Publication: </i>2026 Sep 12. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – Name: Language Label: Language Group: Lang Data: English – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Springer%22">Springer </searchLink><i>Country of Publication: </i>Germany <i>NLM ID: </i>101602699 <i>Publication Model: </i>Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2194-7236 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2221947228%22">21947228 </searchLink><i>NLM ISO Abbreviation: </i>Urolithiasis <i>Subsets: </i>MEDLINE – Name: PublisherInfo Label: Imprint Name(s) Group: PubInfo Data: <i>Original Publication</i>: Berlin : Springer, [2013]- – Name: SubjectMESH Label: MeSH Terms Group: Su Data: <searchLink fieldCode="MM" term="%22beta+Carotene%22">beta Carotene*</searchLink>/<searchLink fieldCode="MM" term="%22beta+Carotene+pharmacology%22">pharmacology</searchLink> <br /><searchLink fieldCode="MM" term="%22beta+Carotene%22">beta Carotene*</searchLink>/<searchLink fieldCode="MM" term="%22beta+Carotene+therapeutic+use%22">therapeutic use</searchLink> <br /><searchLink fieldCode="MM" term="%22NF-kappa+B%22">NF-kappa B*</searchLink>/<searchLink fieldCode="MM" term="%22NF-kappa+B+metabolism%22">metabolism</searchLink> <br /><searchLink fieldCode="MM" term="%22NF-kappa+B%22">NF-kappa B*</searchLink>/<searchLink fieldCode="MM" term="%22NF-kappa+B+antagonists+%26+inhibitors%22">antagonists & inhibitors</searchLink> <br /><searchLink fieldCode="MM" term="%22Calcium+Oxalate%22">Calcium Oxalate*</searchLink>/<searchLink fieldCode="MM" term="%22Calcium+Oxalate+chemistry%22">chemistry</searchLink> <br /><searchLink fieldCode="MM" term="%22Inflammation%22">Inflammation*</searchLink>/<searchLink fieldCode="MM" term="%22Inflammation+drug+therapy%22">drug therapy</searchLink> <br /><searchLink fieldCode="MM" term="%22Nephrocalcinosis%22">Nephrocalcinosis*</searchLink>/<searchLink fieldCode="MM" term="%22Nephrocalcinosis+chemically+induced%22">chemically induced</searchLink> <br /><searchLink fieldCode="MM" term="%22Nephrocalcinosis%22">Nephrocalcinosis*</searchLink>/<searchLink fieldCode="MM" term="%22Nephrocalcinosis+drug+therapy%22">drug therapy</searchLink> <br /><searchLink fieldCode="MM" term="%22Nephrocalcinosis%22">Nephrocalcinosis*</searchLink>/<searchLink fieldCode="MM" term="%22Nephrocalcinosis+pathology%22">pathology</searchLink> <br /><searchLink fieldCode="MM" term="%22Nephrolithiasis%22">Nephrolithiasis*</searchLink>/<searchLink fieldCode="MM" term="%22Nephrolithiasis+drug+therapy%22">drug therapy</searchLink><br /><searchLink fieldCode="MH" term="%22Signal+Transduction%22">Signal Transduction</searchLink>/<searchLink fieldCode="MH" term="%22Signal+Transduction+drug+effects%22">drug effects</searchLink> ; <searchLink fieldCode="MH" term="%22Signal+Transduction%22">Signal Transduction</searchLink>/<searchLink fieldCode="MH" term="%22Signal+Transduction+immunology%22">immunology</searchLink> ; <searchLink fieldCode="MH" term="%22Kidney+Tubules%2C+Proximal%22">Kidney Tubules, Proximal</searchLink>/<searchLink fieldCode="MH" term="%22Kidney+Tubules%2C+Proximal+cytology%22">cytology</searchLink> ; <searchLink fieldCode="MH" term="%22Kidney+Tubules%2C+Proximal%22">Kidney Tubules, Proximal</searchLink>/<searchLink fieldCode="MH" term="%22Kidney+Tubules%2C+Proximal+drug+effects%22">drug effects</searchLink> ; <searchLink fieldCode="MH" term="%22Kidney%22">Kidney</searchLink>/<searchLink fieldCode="MH" term="%22Kidney+pathology%22">pathology</searchLink> ; <searchLink fieldCode="MH" term="%22Kidney%22">Kidney</searchLink>/<searchLink fieldCode="MH" term="%22Kidney+drug+effects%22">drug effects</searchLink> ; <searchLink fieldCode="MH" term="%22Animals%22">Animals</searchLink> ; <searchLink fieldCode="MH" term="%22Mice%22">Mice</searchLink> ; <searchLink fieldCode="MH" term="%22Humans%22">Humans</searchLink> ; <searchLink fieldCode="MH" term="%22Disease+Models%2C+Animal%22">Disease Models, Animal</searchLink> ; <searchLink fieldCode="MH" term="%22Male%22">Male</searchLink> ; <searchLink fieldCode="MH" term="%22Cell+Line%22">Cell Line</searchLink> ; <searchLink fieldCode="MH" term="%22Molecular+Docking+Simulation%22">Molecular Docking Simulation</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Calcium oxalate (CaOx) nephrolithiasis represents the most prevalent form of kidney stone disease and is characterized by persistent renal inflammation and tissue damage. β-Carotene, a naturally occurring carotenoid with well-documented anti-inflammatory properties, has demonstrated beneficial effects in a variety of inflammatory conditions; however, its potential role in CaOx crystal-associated renal injury remains largely unexplored. In this study, the effects of β-carotene on CaOx-induced renal damage were evaluated using both cellular and animal models. In human renal proximal tubular epithelial (HK-2) cells, β-carotene effectively alleviated calcium oxalate monohydrate (COM)-induced injury, decreased kidney injury molecule-1 (KIM-1) expression, and reduced the production of pro-inflammatory mediators, including TNF-α, IL-1β, IL-6, and MCP-1. Similarly, in a glyoxylate-induced nephrocalcinosis mouse model, β-carotene attenuated CaOx crystal accumulation, improved renal histopathological alterations and functional impairment, and suppressed inflammatory responses. To investigate the underlying mechanisms, network pharmacology and molecular docking analyses were conducted. A total of 145 overlapping targets were identified, and enrichment analyses identified NF-κB signaling as one of the candidate pathways potentially involved in the protective effects of β-carotene. Molecular docking analysis suggested favorable binding affinities between β-carotene and several key targets. Experimental validation demonstrated that β-carotene markedly inhibited NF-κB activation in both in vitro and in vivo settings, whereas pharmacological activation of NF-κB partially abolished its beneficial effects. Taken together, these findings indicate that β-carotene ameliorates CaOx crystal-induced renal injury and inflammation, at least in part through suppression of NF-κB signaling, and may offer a potential basis for the development of novel preventive and therapeutic approaches for kidney stone disease.<br /> (© 2026. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) – Name: Abstract Label: Competing Interests Group: Ab Data: Declarations. Competing interests: The authors declare no competing interests. – Name: Ref Label: References Group: RefInfo Data: J Urol. 2005 Mar;173(3):848-57. (PMID: <searchLink fieldCode="PM" term="%2215711292%22">15711292)</searchLink><br />Int J Urol. 2008 Feb;15(2):115-20. (PMID: <searchLink fieldCode="PM" term="%2218269444%22">18269444)</searchLink><br />Cell Mol Life Sci. 2023 Sep 23;80(10):301. (PMID: <searchLink fieldCode="PM" term="%2237740796%22">37740796)</searchLink><br />Nat Rev Nephrol. 2021 Jun;17(6):417-433. (PMID: <searchLink fieldCode="PM" term="%2233514941%22">33514941)</searchLink><br />Eur J Med Res. 2025 Dec 10;30(1):1224. (PMID: <searchLink fieldCode="PM" term="%2241372793%22">41372793)</searchLink><br />Phytomedicine. 2025 Jan;136:156302. (PMID: <searchLink fieldCode="PM" term="%2239662099%22">39662099)</searchLink><br />J Nephrol. 2017 Apr;30(2):227-233. (PMID: <searchLink fieldCode="PM" term="%2226969574%22">26969574)</searchLink><br />Int Urol Nephrol. 2024 Feb;56(2):423-431. (PMID: <searchLink fieldCode="PM" term="%2237740155%22">37740155)</searchLink><br />Theranostics. 2020 Jun 5;10(16):7319-7334. (PMID: <searchLink fieldCode="PM" term="%2232641994%22">32641994)</searchLink><br />Int Immunopharmacol. 2022 Jun;107:108677. (PMID: <searchLink fieldCode="PM" term="%2235255299%22">35255299)</searchLink><br />Curr Drug Targets. 2025;26(9):591-612. (PMID: <searchLink fieldCode="PM" term="%2240353475%22">40353475)</searchLink><br />J Urol. 2013 Mar;189(3):803-11. (PMID: <searchLink fieldCode="PM" term="%2223022011%22">23022011)</searchLink><br />Front Pharmacol. 2022 Nov 03;13:1041117. (PMID: <searchLink fieldCode="PM" term="%2236408256%22">36408256)</searchLink><br />J Am Soc Nephrol. 2009 Oct;20(10):2253-9. (PMID: <searchLink fieldCode="PM" term="%2219679672%22">19679672)</searchLink><br />Arch Biochem Biophys. 2018 Aug 15;652:18-26. (PMID: <searchLink fieldCode="PM" term="%2229885291%22">29885291)</searchLink><br />EBioMedicine. 2019 Dec;50:366-378. (PMID: <searchLink fieldCode="PM" term="%2231735555%22">31735555)</searchLink><br />Pak J Biol Sci. 2009 Aug 15;12(16):1140-5. (PMID: <searchLink fieldCode="PM" term="%2219899325%22">19899325)</searchLink><br />Food Funct. 2024 Dec 9;15(24):12033-12046. (PMID: <searchLink fieldCode="PM" term="%2239563640%22">39563640)</searchLink><br />Int J Biol Sci. 2025 Apr 22;21(7):3099-3121. (PMID: <searchLink fieldCode="PM" term="%2240384863%22">40384863)</searchLink><br />Int J Urol. 2008 Oct;15(10):924-8. (PMID: <searchLink fieldCode="PM" term="%2218721209%22">18721209)</searchLink><br />Rev Urol. 2010 Spring;12(2-3):e86-96. (PMID: <searchLink fieldCode="PM" term="%2220811557%22">20811557)</searchLink><br />J Food Sci. 2023 Jan;88(1):491-502. (PMID: <searchLink fieldCode="PM" term="%2236448622%22">36448622)</searchLink><br />Chin J Nat Med. 2023 May;21(5):323-332. (PMID: <searchLink fieldCode="PM" term="%2237245871%22">37245871)</searchLink><br />J Agric Food Chem. 2025 Jan 15;73(2):1542-1562. (PMID: <searchLink fieldCode="PM" term="%2239741421%22">39741421)</searchLink><br />World J Urol. 2017 Sep;35(9):1301-1320. (PMID: <searchLink fieldCode="PM" term="%2228213860%22">28213860)</searchLink><br />PLoS One. 2023 Apr 5;18(4):e0283779. (PMID: <searchLink fieldCode="PM" term="%2237018237%22">37018237)</searchLink><br />Chem Biol Interact. 2017 Dec 25;278:114-122. (PMID: <searchLink fieldCode="PM" term="%2229054323%22">29054323)</searchLink><br />Urolithiasis. 2025 Jul 2;53(1):134. (PMID: <searchLink fieldCode="PM" term="%2240601009%22">40601009)</searchLink><br />Adv Sci (Weinh). 2026 Aug;13(43):e75585. (PMID: <searchLink fieldCode="PM" term="%2242107057%22">42107057)</searchLink><br />Adv Chronic Kidney Dis. 2015 Jul;22(4):266-72. (PMID: <searchLink fieldCode="PM" term="%2226088070%22">26088070)</searchLink><br />J Am Soc Nephrol. 2017 Mar;28(3):761-768. (PMID: <searchLink fieldCode="PM" term="%2227612997%22">27612997)</searchLink><br />Adv Urol. 2018 Feb 4;2018:3068365. (PMID: <searchLink fieldCode="PM" term="%2229515627%22">29515627)</searchLink><br />Transl Androl Urol. 2014 Sep;3(3):285-95. (PMID: <searchLink fieldCode="PM" term="%2226816779%22">26816779)</searchLink><br />J Urol. 2022 Jan;207(1):144-151. (PMID: <searchLink fieldCode="PM" term="%2234428923%22">34428923)</searchLink><br />J Food Sci. 2021 May;86(5):2118-2130. (PMID: <searchLink fieldCode="PM" term="%2233884622%22">33884622)</searchLink><br />J Urol. 2010 Sep;184(3):1189-96. (PMID: <searchLink fieldCode="PM" term="%2220663521%22">20663521)</searchLink><br />Phytomedicine. 2024 Dec;135:156145. (PMID: <searchLink fieldCode="PM" term="%2239461201%22">39461201)</searchLink><br />Nat Rev Dis Primers. 2016 Feb 25;2:16008. (PMID: <searchLink fieldCode="PM" term="%2227188687%22">27188687)</searchLink><br />Nutr Res. 2014 Nov;34(11):907-29. (PMID: <searchLink fieldCode="PM" term="%2225134454%22">25134454)</searchLink> – Name: SubjectMinor Label: Contributed Indexing Group: Data: <i>Keywords: </i>Kidney stones; Network pharmacology NF-κΒ; β-Carotene – Name: NumberCAS Label: Substance Nomenclature Group: ID Data: 01YAE03M7J (beta Carotene)<br />0 (NF-kappa B)<br />2612HC57YE (Calcium Oxalate) – Name: DateEntry Label: Entry Date(s) Group: Date Data: <i>Date Created: </i>20260912 <i>Date Completed: </i>20260912 <i>Latest Revision: </i>20261008 – Name: DateUpdate Label: Update Code Group: Date Data: 20261008 – Name: DOI Label: DOI Group: ID Data: 10.1007/s00240-026-02053-7 – Name: AN Label: PMID Group: ID Data: 42730918 |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s00240-026-02053-7 Languages: – Code: eng Text: English Subjects: – SubjectFull: Signal Transduction drug effects Type: general – SubjectFull: Signal Transduction immunology Type: general – SubjectFull: Kidney Tubules, Proximal cytology Type: general – SubjectFull: Kidney Tubules, Proximal drug effects Type: general – SubjectFull: Kidney pathology Type: general – SubjectFull: Kidney drug effects Type: general – SubjectFull: Animals Type: general – SubjectFull: Mice Type: general – SubjectFull: Humans Type: general – SubjectFull: Disease Models, Animal Type: general – SubjectFull: Male Type: general – SubjectFull: Cell Line Type: general – SubjectFull: Molecular Docking Simulation Type: general – SubjectFull: beta Carotene pharmacology Type: general – SubjectFull: beta Carotene therapeutic use Type: general – SubjectFull: NF-kappa B metabolism Type: general – SubjectFull: NF-kappa B antagonists & inhibitors Type: general – SubjectFull: Calcium Oxalate chemistry Type: general – SubjectFull: Inflammation drug therapy Type: general – SubjectFull: Nephrocalcinosis chemically induced Type: general – SubjectFull: Nephrocalcinosis drug therapy Type: general – SubjectFull: Nephrocalcinosis pathology Type: general – SubjectFull: Nephrolithiasis drug therapy Type: general Titles: – TitleFull: β-carotene attenuates calcium oxalate crystal-induced renal injury through suppression of NF-κB-mediated inflammation. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Su M – PersonEntity: Name: NameFull: Guan Y – PersonEntity: Name: NameFull: Wei H – PersonEntity: Name: NameFull: Chen L – PersonEntity: Name: NameFull: Dong W IsPartOfRelationships: – BibEntity: Dates: – D: 12 M: 09 Text: 2026 Sep 12 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 2194-7236 Numbering: – Type: volume Value: 54 – Type: issue Value: 1 Titles: – TitleFull: Urolithiasis Type: main |
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