The toxic saponin - solanine and its properties
DOI:
https://doi.org/10.56782/pps.430Keywords:
solanine, phytochemical, Solanum tuberosum, toxicity, biological propertiesAbstract
α-Solanine is a steroidal glycoalkaloid naturally occurring in plants of the Solanaceae family, such as potatoes, tomatoes, and eggplants. Due to its toxicity, it serves a protective function by deterring herbivores. High concentrations of this compound are found in the green parts of potato tubers. Due to the widespread occurrence of α-solanine in nature, it is often unknowingly consumed by a large number of people. Ingesting this compound in large amounts can lead to poisoning, which manifests as gastrointestinal and neurological symptoms. In extreme cases, excessive solanine consumption can be fatal. Despite documented cases of poisoning, α-solanine exhibits potentially beneficial pharmacological properties. This compound is being investigated for its anticancer and anti-inflammatory effects, as well as its potential use in the treatment of osteoarthritis and neurodegenerative diseases. However, its toxicity significantly limits its possible applications as a therapeutic agent. The objective of this study was to provide an overview of the biological properties of solanine and its potential applications in medical sciences.
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1. Winkiel, M. J.; Chowański, S.; Słocińska, M. Anticancer Activity of Glycoalkaloids from Solanum Plants: A Review. Front. Pharmacol. 2022, 13, Art. No: 979451. DOI: 10.3389/FPHAR.2022.979451
2. Duggan, T.; Dawid, C.; Baur, S.; Hofmann, T. Characterization of Bitter and Astringent Off-Taste Compounds in Potato Fibers. J. Agric. Food Chem. 2020, 68 (41), 11524–11534. DOI: 10.1021/ACS.JAFC.0C04853
3. Akiyama, R.; Watanabe, B.; Nakayasu, M.; Lee, H. J.; Kato, J.; Umemoto, N.; Muranaka, T.; Saito, K.; Sugimoto, Y.; Mizutani, M. The Biosynthetic Pathway of Potato Solanidanes Diverged from That of Spirosolanes Due to Evolution of a Dioxygenase. Nat. Commun. 2021, 12 (1), Art. No: 1300. DOI: 10.1038/s41467-021-21546-0
4. Ohyama, K.; Okawa, A.; Moriuchi, Y.; Fujimoto, Y. Biosynthesis of Steroidal Alkaloids in Solanaceae Plants: Involvement of an Aldehyde Intermediate during C-26 Amination. Phytochemistry 2013, 89, 26–31. DOI: 10.1016/J.PHYTOCHEM.2013.01.010
5. Baur, S.; Frank, O.; Hausladen, H.; Hückelhoven, R.; Hofmann, T.; Eisenreich, W.; Dawid, C. Biosynthesis of α-Solanine and α-Chaconine in Potato Leaves (Solanum tuberosum L.) – A 13CO2 Study. Food Chem. 2021, 365, Art. No: 130461. DOI: 10.1016/J.FOODCHEM.2021.130461
6. Ostrý, V.; Ruprich, J.; Skarkova, J. Glycoalkaloids in Potato Tubers: The Effect of Peeling and Cooking in Salted Water. Acta Aliment. 2010, 39 (2), 130–135. DOI: 10.1556/AALIM.39.2010.2.4
7. Friedman, M. Potato Glycoalkaloids and Metabolites: Roles in the Plant and in the Diet. J. Agric. Food Chem. 2006, 54 (23), 8655–8681. DOI: 10.1021/JF061471T
8. Nandi, S.; Sikder, R.; Nag, A.; Khatua, S.; Sen, S.; Chakraborty, N.; Naskar, A.; Zhakipbekov, K.; Acharya, K.; Habtemariam, S.; Arslan Ateşşahin, D.; Goloshvili, T.; Ahmed Aldahish, A.; Sharifi-Rad, J.; Calina, D. Updated Aspects of Alpha-Solanine as a Potential Anticancer Agent: Mechanistic Insights and Future Directions. Food Sci. Nutr. 2024, 12 (10), 7088–7107. DOI: 10.1002/FSN3.4221
9. Boullion Lagrange, E. J. B.; Cadet, C. L.; Planche, L. A.; Boullay, P. F. G.; Boudet, J. P.; Viray, J. J.; Pelletier, J.; Vogel, A. Journal de pharmacie et des sciences accessoires. Imprimeur-Libraire. 1820, 6, Art. No: 18.
10. Karaca, M.; Erbaş, O. Solanine Poisoning: Effects, Risks, and Management Strategies. J. Exp. Basic Med. Sci. 2024, 5 (2), 189-193. DOI: 10.5606/JEBMS.2024.1090
11. Jensen, P. H.; Pedersen, R. B.; Svensmark, B.; Strobel, B. W.; Jacobsen, O. S.; Hansen, H. C. B. Degradation of the Potato Glycoalkaloid α-Solanine in Three Agricultural Soils. Chemosphere 2009, 76 (8), 1150–1155. DOI: 10.1016/J.CHEMOSPHERE.2009.04.008
12. Smith, D. B.; Roddick, J. G.; Jones, J. L. Potato Glycoalkaloids: Some Unanswered Questions. Trends Food Sci. Technol. 1996, 7, 126–131. DOI: 10.1016/0924-2244(96)10013-3
13. Butnaru, C.; Vlase, L.; Lazăr, D.; Agoroaei, L.; Lazăr, M. I. HPLC/MS analysis of solanine in Physalis alkekengi and Solanum dulcamara. Farmacia 2011, 59 (2), 172–178.
14. Li, Z.; Zhou, B.; Ding, Y.; Liu, X. Extraction and determination of α-solanine in eggplant fruits. J. Appl. Hortic. 2009, 11, 59–63. DOI: 10.37855/jah.2009.v11i01.12
15. Itkin, M.; Rogachev, I.; Alkan, N.; Rosenberg, T.; Malitsky, S.; Masini, L.; Meir, S.; Iijima, Y.; Aoki, K.; de Vos, R.; Prusky, D.; Burdman, S.; Beekwilder, J.; Aharoni, A. Glycoalkaloid Metabolism Is Required for Steroidal Alkaloid Glycosylation and Prevention of Phytotoxicity in Tomato. Plant Cell 2011, 23 (12), 4507–4525. DOI: 10.1105/TPC.111.088732
16. Willimott, S. G. An Investigation of Solanine Poisoning. Analyst 1933, LVIII (689), 431–439.
17. Patil, B. C.; Sharma, R. P.; Salunkhe, D. K.; Salunkhe, K. Evaluation of Solanine Toxicity; Pergamon Press, 1972; Vol. 10.
18. Nishie, K.; Gumbmann, M. R.; Keyl, A. C. Pharmacology of Solanine; 1971; Vol. 19.
19. Al Masaoud, F. S.; Alharbi, A.; Behir, M. M.; Siddiqui, A. F.; Al-Murayeh, L. M.; Al Dail, A.; Siddiqui, R. A Challenging Case of Suspected Solanine Toxicity in an Eleven-Year-Old Saudi Boy. J. Fam. Med. Prim. Care 2022, 11 (7), 4039–4041. DOI: 10.4103/JFMPC.JFMPC_1159_21
20. Barceloux, D. G. Potatoes, Tomatoes, and Solanine Toxicity (Solanum tuberosum L., Solanum lycopersicum L.). Dis.-a-Mon. 2009, 55 (6), 391–402. DOI: 10.1016/J.DISAMONTH.2009.03.009
21. Langkilde, S.; Schrøder, M.; Stewart, D.; Meyer, O.; Conner, S.; Davies, H.; Poulsen, M. Acute Toxicity of High Doses of the Glycoalkaloids, α-Solanine and α-Chaconine, in the Syrian Golden Hamster. J. Agric. Food Chem. 2008, 56 (18), 8753–8760. DOI: 10.1021/jf8012794
22. Fabiansson, S. U. Public Health Measures: Assessment of Novel Foods and Ingredients. Encyclopedia of Food Safety 2014, 4, 62–67. DOI: 10.1016/B978-0-12-378612-8.00350-4
23. Ekmekci, E.; Esercan, A.; Yanar, O.; Yakar, Y.; Yasar, E. Is There Any Association between Blood Glycoalkaloid Levels and Anencephaly in Human? Clin. Biochem. 2024, 131–132, Art. No: 110809. DOI: 10.1016/J.CLINBIOCHEM.2024.110809
24. Schrenk, D.; Bignami, M.; Bodin, L.; Chipman, J. K.; del Mazo, J.; Hogstrand, C.; Hoogenboom, L.; Leblanc, J. C.; Nebbia, C. S.; Nielsen, E.; Ntzani, E.; Petersen, A.; Sand, S.; Schwerdtle, T.; Vleminckx, C.; Wallace, H.; Brimer, L.; Cottrill, B.; Dusemund, B.; Mulder, P.; Vollmer, G.; Binaglia, M.; Ramos Bordajandi, L.; Riolo, F.; Roldán-Torres, R.; Grasl-Kraupp, B. Risk Assessment of Glycoalkaloids in Feed and Food, in Particular in Potatoes and Potato-derived Products. EFSA J. 2020, 18 (8), Art. No: e06222. DOI: 10.2903/J.EFSA.2020.6222
25. Morris, T. Case of Poisoning by Potatoe-Berries. Br. Med. J. 1859, 719–720.
26. Hansen, A. A. Two Fatal Cases of Potato Poisoning. Science 1925, 61 (1578), 340–341. DOI: 10.1126/SCIENCE.61.1578.340
27. Wang, L.; Zhang, L.; Ying, C.; Jin, X.; Ying, M.; Chen, H.; Zhu, D. Cryptogenic Organizing Pneumonia Caused by Solanine: A Case Report. Medicine 2024, 103 (39), Art. No: e39807. DOI: 10.1097/MD.0000000000039807
28. Ceha, L. J.; Presperin, C.; Young, E.; Allswede, M.; Erickson, T. B. Anticholinergic Toxicity from Nightshade Berry Poisoning Responsive to Physostigmine. J. Emerg. Med. 1997, 15 (1), 65–69. DOI: 10.1016/S0736-4679(96)00244-2
29. Huang, S. T.; Su, Y. J.; Chien, D. K.; Li, E. J.; Chang, W. H. Solanum erianthum Intoxication Mimicking an Acute Cerebrovascular Disease. Am. J. Emerg. Med. 2009, 27 (2), 249.e1–249.e2. DOI: 10.1016/J.AJEM.2008.05.026
30. Kees, M.; Beckel, N.; Sharp, C. Successful Treatment of Solanum dulcamara Intoxication in a Labrador Retriever Puppy. Can. Vet. J. 2015, 56 (12), Art. No: 1283.
31. Norman, T. E.; Chaffin, M. K.; Norton, P. L.; Coleman, M. C.; Stoughton, W. B.; Mays, T. Concurrent Ivermectin and Solanum spp. Toxicosis in a Herd of Horses. J. Vet. Intern. Med. 2012, 26 (6), 1439–1442. DOI: 10.1111/J.1939-1676.2012.00996.X
32. Baker, D. C.; Keeler, R. F.; Gaffield, W. P. Mechanism of Death in Syrian Hamsters Gavaged Potato Sprout Material. Toxicol. Pathol. 1988, 16 (3), 333–339. DOI: 10.1177/019262338801600304
33. Nigg, H. N.; Ramos, L. E.; Graham, E. M.; Sterling, J.; Brown, S.; Cornell, J. A. Inhibition of Human Plasma and Serum Butyrylcholinesterase (EC 3.1.1.8) by α-Chaconine and α-Solanine. Fundam. Appl. Toxicol. 1996, 33 (2), 272–281. DOI: 10.1006/faat.1996.0165
34. McGehee, D. S.; Krasowski, M. D.; Fung, D. L.; Wilson, B.; Gronert, G. A.; Moss, J. Cholinesterase Inhibition by Potato Glycoalkaloids Slows Mivacurium Metabolism. Anesthesiology 2000, 93 (2), 510–519. DOI: 10.1097/00000542-200008000-00031
35. Orgell, W. H.; Vaidya, K. A.; Dahm, P. A. Inhibition of Human Plasma Cholinesterase in Vitro by Extracts of Solanaceous Plants. Science 1958, 128 (3332), 1135–1136. DOI: 10.1126/SCIENCE.128.3332.1136
36. Obaid Saleh, B. H.; Salman, M. D.; Salman, A. D.; Alardhi, S. M.; Mohammed, M. M.; Gyurika, I. G.; Le, P. C.; Ali, O. I. In Silico Analysis of the Use of Solanine Derivatives as a Treatment for Alzheimer’s Disease. Heliyon 2024, 10 (11), Art. No: e32209. DOI: 10.1016/J.HELIYON.2024.E32209
37. Alozie, S. O.; Sharma, R. P.; Salunkhe, D. K. Inhibition of Rat Cholinesterase Isoenzymes in Vitro and in Vivo by the Potato Alkaloid, α-Chaconine. J. Food Biochem. 1978, 2 (3), 259–276. DOI: 10.1111/J.1745-4514.1978.TB00621.X
38. Langkilde, S.; Mandimika, T.; Schrøder, M.; Meyer, O.; Slob, W.; Peijnenburg, A.; Poulsen, M. A 28-Day Repeat Dose Toxicity Study of Steroidal Glycoalkaloids, α-Solanine and α-Chaconine in the Syrian Golden Hamster. Food Chem. Toxicol. 2009, 47 (6), 1099–1108. DOI: 10.1016/j.fct.2009.01.045
39. Pacifico, D.; Lanzanova, C.; Pagnotta, E.; Bassolino, L.; Mastrangelo, A. M.; Marone, D.; Matteo, R.; Lo Scalzo, R.; Balconi, C. Sustainable Use of Bioactive Compounds from Solanum tuberosum and Brassicaceae Wastes and By-Products for Crop Protection—A Review. Molecules 2021, 26 (8), Art. No: 2174. DOI: 10.3390/MOLECULES26082174
40. Gao, S. Y.; Wang, Q. J.; Ji, Y. Bin. Effect of Solanine on the Membrane Potential of Mitochondria in HepG2 Cells and [Ca2+]i in the Cells. World J. Gastroenterol. 2006, 12 (21), 3359–3367. DOI: 10.3748/wjg.v12.i21.3359
41. Park, S.; Park, M. Y.; Song, G.; Lim, W. Alpha-Solanine Inhibits Cell Proliferation via Mitochondrial Dysfunction and Inhibin Synthesis in Mouse Testis In Vitro and In Vivo. Chemosphere 2019, 235, 271–279. DOI: 10.1016/J.CHEMOSPHERE.2019.06.172
42. Keukens, E. A. J.; de Vrije, T.; van den Boom, C.; de Waard, P.; Plasman, H. H.; Thiel, F.; Chupin, V.; Jongen, W. M. F.; de Kruijff, B. Molecular Basis of Glycoalkaloid Induced Membrane Disruption. Biochim. Biophys. Acta, Biomembr. 1995, 1240 (2), 216–228. DOI: 10.1016/0005-2736(95)00186-7
43. Toyoda, M.; Rausch, W. D.; Inoue, K.; Ohno, Y.; Fujiyama, Y.; Takagi, K.; Saito, Y. Comparison of Solanaceous Glycoalkaloids-Evoked Ca2+ Influx in Different Types of Cultured Cells. Toxicol. In Vitro 1991, 5 (4), 347–351. DOI: 10.1016/0887-2333(91)90012-3
44. Yamashoji, S.; Matsuda, T. Synergistic Cytotoxicity Induced by α-Solanine and α-Chaconine. Food Chem. 2013, 141 (2), 669–674. DOI: 10.1016/J.FOODCHEM.2013.03.104
45. Mensinga, T. T.; Sips, A. J. A. M.; Rompelberg, C. J. M.; Van Twillert, K.; Meulenbelt, J.; Van Den Top, H. J.; Van Egmond, H. P. Potato Glycoalkaloids and Adverse Effects in Humans: An Ascending Dose Study. Regul. Toxicol. Pharmacol. 2005, 41 (1), 66–72. DOI: 10.1016/J.YRTPH.2004.09.004
46. Roddick, J. G.; Rijnenberg, A. L. Synergistic Interaction between the Potato Glycoalkaloids α-Solanine and α-Chaconine in Relation to Lysis of Phospholipid/Sterol Liposomes. Phytochemistry 1987, 26 (5), 1325–1328. DOI: 10.1016/S0031-9422(00)81804-X
47. Manrique-Moreno, M.; Londoño-Londoño, J.; Jemioła-Rzemińska, M.; Strzałka, K.; Villena, F.; Avello, M.; Suwalsky, M. Structural Effects of the Solanum Steroids Solasodine, Diosgenin and Solanine on Human Erythrocytes and Molecular Models of Eukaryotic Membranes. Biochim. Biophys. Acta, Biomembr. 2014, 1838 (1 Pt B), 266–277. DOI: 10.1016/J.BBAMEM.2013.08.003
48. Blankemeyer, J. T.; Atherton, R.; Friedman, M. Effect of Potato Glycoalkaloids α-Chaconine and α-Solanine on Sodium Active Transport in Frog Skin. J. Agric. Food Chem. 1995, 43 (3), 636–639. DOI: 10.1021/JF00051A015/ASSET/JF00051A015.FP.PNG_V03
49. Caldwell, K. A.; Grosjean, O. K.; Henika, P. R.; Friedman, M. Hepatic Ornithine Decarboxylase Induction by Potato Glycoalkaloids in Rats. Food Chem. Toxicol. 1991, 29 (8), 531–535. DOI: 10.1016/0278-6915(91)90045-9
50. Gaffield, W.; Keeler, R. F. Induction of Terata in Hamsters by Solanidane Alkaloids Derived from Solanum tuberosum. Chem. Res. Toxicol. 1996, 9 (2), 426–433. DOI: 10.1021/TX950091R
51. Mun, A. M.; Barden, E. S.; Wilson, J. M.; Hogan, J. M. Teratogenic Effects in Early Chick Embryos of Solanine and Glycoalkaloids from Potatoes Infected with Late-blight, Phytophthora infestans. Teratology 1975, 11 (1), 73–77. DOI: 10.1002/tera.1420110109
52. Jelínek, R.; Kyzlink, V.; Blattný, C. An Evaluation of the Embryotoxic Effects of Blighted Potatoes on Chicken Embryos. Teratology 1976, 14 (3), 335–342. DOI: 10.1002/TERA.1420140309
53. Rayburn, J. R.; Friedman, M.; Bantle, J. A. Synergistic Interaction of Glycoalkaloids α-Chaconine and α-Solanine on Developmental Toxicity in Xenopus Embryos. Food Chem. Toxicol. 1995, 33 (12), 1013–1019. DOI: 10.1016/0278-6915(95)00081-X
54. Crawford, L.; Kocan, R. M. Steroidal Alkaloid Toxicity to Fish Embryos. Toxicol. Lett. 1993, 66 (2), 175–181. DOI: 10.1016/0378-4274(93)90092-C
55. Lin, T.; Oqani, R. K.; Lee, J. E.; Kang, J. W.; Kim, S. Y.; Cho, E. S.; Jeong, Y. D.; Baek, J. J.; Jin, D. Il. α-Solanine Impairs Oocyte Maturation and Quality by Inducing Autophagy and Apoptosis and Changing Histone Modifications in a Pig Model. Reprod. Toxicol. 2018, 75, 96–109. DOI: 10.1016/J.REPROTOX.2017.12.005
56. Allen, J. R.; Marlar, R. J.; Chesney, C. F.; Helgeson, J. P.; Kelman, A.; Weckel, K. G.; Traisman, E.; White, J. W. Teratogenicity Studies on Late Blighted Potatoes in Nonhuman Primates (Macaca mulatta and Saguinus labiatus). Teratology 1977, 15 (1), 17–23. DOI: 10.1002/TERA.1420150103
57. Ventrella, E.; Adamski, Z.; Chudzińska, E.; Miądowicz-Kobielska, M.; Marciniak, P.; Büyükgüzel, E.; Büyükgüzel, K.; Erdem, M.; Falabella, P.; Scrano, L.; Bufo, S. A. Solanum tuberosum and Lycopersicon esculentum Leaf Extracts and Single Metabolites Affect Development and Reproduction of Drosophila melanogaster. PLoS One 2016, 11 (5), Art. No: e0155958. DOI: 10.1371/JOURNAL.PONE.0155958
58. Rahaman, M. M.; , Hossain, R.; Herrera‐Bravo, J.; Islam, M. T.; Atolani, O.; Adeyemi, O. S.; Owolodun, O. A.; Kambizi, L.; Daştan, S. D.; Calina, D.; Sharifi‐Rad, J. Natural antioxidants from some fruits, seeds, foods, natural products, and associated health benefits: An update. Food Sci. Nutr. 2023, 11 (4), 1657–1670. DOI: 10.1002/FSN3.3217
59. Arslan, A. K. K.; Yerer, M. B. α-Chaconine and α-Solanine Inhibit RL95-2 Endometrium Cancer Cell Proliferation by Reducing Expression of Akt (Ser473) and ERα (Ser167). Nutrients 2018, 10 (6), Art. No: 672. DOI: 10.3390/NU10060672
60. Mohsenikia, M.; Alizadeh, A. M.; Khodayari, S.; Khodayari, H.; Kouhpayeh, S. A.; Karimi, A.; Zamani, M.; Azizian, S.; Mohagheghi, M. A. The Protective and Therapeutic Effects of Alpha-Solanine on Mice Breast Cancer. Eur. J. Pharmacol. 2013, 718 (1–3), 1–9. DOI: 10.1016/J.EJPHAR.2013.09.015
61. Yan, X.; Li, M.; Chen, L.; Peng, X.; Que, Z. J.; An, H. M.; Shen, K. P.; Hu, B. α-Solanine Inhibits Growth and Metastatic Potential of Human Colorectal Cancer Cells. Oncol. Rep. 2020, 43 (5), 1387–1396. DOI: 10.3892/OR.2020.7519
62. Zou, T.; Gu, L.; Yang, L.; Wei, J.; Zhao, Y.; Shen, J.; Li, M.; Wu, X.; Du, F.; Chen, Y.; Ye, Y.; Xiao, Z.; Wu, Z. Alpha-Solanine Anti-Tumor Effects in Non-Small Cell Lung Cancer Through Regulating the Energy Metabolism Pathway. Recent Pat. Anticancer Drug Discov. 2022, 17 (4), 396–409. DOI: 10.2174/1574892817666220113144635
63. Shen, K. H.; Liao, A. C. H.; Hung, J. H.; Lee, W. J.; Hu, K. C.; Lin, P. T.; Liao, R. F.; Chen, P. S. α-Solanine Inhibits Invasion of Human Prostate Cancer Cell by Suppressing Epithelial-Mesenchymal Transition and MMPs Expression. Molecules 2014, 19 (8), 11896–11914. DOI: 10.3390/MOLECULES190811896
64. El-Daly, S. M.; Gouhar, S. A.; Gamal-Eldeen, A. M.; Abdel Hamid, F. F.; Ashour, M. N.; Hassan, N. S. Synergistic Effect of α-Solanine and Cisplatin Induces Apoptosis and Enhances Cell Cycle Arrest in Human Hepatocellular Carcinoma Cells. Anticancer Agents Med. Chem. 2019, 19 (18), 2197–2210. DOI: 10.2174/1871520619666190930123520
65. Pan, B.; Zhong, W.; Deng, Z.; Lai, C.; Chu, J.; Jiao, G.; Liu, J.; Zhou, Q. Inhibition of Prostate Cancer Growth by Solanine Requires the Suppression of Cell Cycle Proteins and the Activation of ROS/P38 Signaling Pathway. Cancer Med. 2016, 5 (11), Art. No: 3214. DOI: 10.1002/CAM4.916
66. Prasad, P.; Jaber, M.; Alahmadi, T. A.; Almoallim, H. S.; Ramu, A. K. Solanine Inhibits Proliferation and Angiogenesis and Induces Apoptosis through Modulation of EGFR Signaling in KB-ChR-8-5 Multidrug-Resistant Oral Cancer Cells. J. Clin. Med. 2024, 13 (15), Art. No: 4493. DOI: 10.3390/JCM13154493
67. Ma, X.; Li, Y.; Liang, D.; Jiang, F.; Zhang, L.; Song, W.; Wan, B.; Xia, C.; Lu, Q. Solanine Induces Ferroptosis in Colorectal Cancer Cells through ALOX12B/ADCY4 Molecular Axis. J. Pharm. Pharmacol. 2024, 76 (3), 224–235. DOI: 10.1093/JPP/RGAD122
68. Gao, J.; Ying, Y.; Wang, J.; Cui, Y. Solanine Inhibits Immune Escape Mediated by Hepatoma Treg Cells via the TGFβ/Smad Signaling Pathway. Biomed. Res. Int. 2020, 2020, Art. No: 9749631. DOI: 10.1155/2020/9749631
69. Lv, C.; Kong, H.; Dong, G.; Liu, L.; Tong, K.; Sun, H.; Chen, B.; Zhang, C.; Zhou, M. Antitumor Efficacy of α-Solanine against Pancreatic Cancer In Vitro and In Vivo. PLoS One 2014, 9 (2), Art. No: e87868. DOI: 10.1371/JOURNAL.PONE.0087868
70. Yang, J.; Hao, T.; Sun, J.; Wei, P.; Zhang, H. Long Noncoding RNA GAS5 Modulates α-Solanine-Induced Radiosensitivity by Negatively Regulating miR-18a in Human Prostate Cancer Cells. Biomed. Pharmacother. 2019, 112, Art No: 108656. DOI: 10.1016/J.BIOPHA.2019.108656
71. Wang, Y.; Wu, J.; Guo, W.; Sun, Q.; Chen, X.; Zang, W.; Dong, Z.; Zhao, G. α-Solanine Modulates the Radiosensitivity of Esophageal Cancer Cells by Inducing MicroRNA 138 Expression. Cell. Physiol. Biochem. 2016, 39 (3), 996–1010. DOI: 10.1159/000447807
72. Ukwubile, C. A.; Ikpefan, E. O.; Famurewa, A. C. Role of Chitosan-Loaded Solanine Glycoalkaloid from Solanum scabrum Mill. Leaf Extract as Anti-Inflammatory and In Vitro Anticancer Agents. Turk. J. Pharm. Sci. 2023, 20 (4), 240–252. DOI: 10.4274/TJPS.GALENOS.2022.03837
73. Asgaritarghi, G.; Farsani, S. S. M.; Sadeghizadeh, D.; Najafi, F.; Sadeghizadeh, M. Anti-Cancer Role of Dendrosomal Nano Solanine in Chronic Myelogenous Leukemia Cell Line through Attenuation of PI3K/AKT/MTOR Signaling Pathway and Inhibition of HTERT Expression. Curr. Mol. Pharmacol. 2023, 16 (5), 592-608. DOI: 10.2174/1874467215666220516143155
74. Shin, J. S.; Lee, K. G.; Lee, H. H.; Lee, H. J.; An, H. J.; Nam, J. H.; Jang, D. S.; Lee, K. T. α-Solanine Isolated From Solanum tuberosum L. Cv Jayoung Abrogates LPS-Induced Inflammatory Responses via NF-κB Inactivation in RAW 264.7 Macrophages and Endotoxin-Induced Shock Model in Mice. J. Cell. Biochem. 2016, 117 (10), 2327–2339. DOI: 10.1002/JCB.25530
75. Zhao, L.; Wang, L.; Di, S.-N.; Xu, Q.; Ren, Q.-C.; Chen, S.-Z.; Huang, N.; Jia, D.; Shen, X.-F. Steroidal Alkaloid Solanine A from Solanum nigrum Linn. Exhibits Anti-Inflammatory Activity in Lipopolysaccharide/Interferon γ-Activated Murine Macrophages and Animal Models of Inflammation. Biomed. Pharmacother. 2018, 105, 606–615. DOI: 10.1016/J.BIOPHA.2018.06.019
76. Piana, M.; Camponogara, C.; Boligon, A. A.; Oliveira, S. M. Solanum paranense Extracts and Solanine Present Anti-Inflammatory Activity in an Acute Skin Inflammation Model in Mice. Evid. Based Complement. Alternat. Med. 2017, 2017, Art. No: 4295680. DOI: 10.1155/2017/4295680
77. Zhou, J.; Wu, J.; Fu, F.; Yao, S.; Zheng, W.; Du, W.; Luo, H.; Jin, H.; Tong, P.; Wu, C.; Ruan, H. α-Solanine Attenuates Chondrocyte Pyroptosis to Improve Osteoarthritis via Suppressing NF-κB Pathway. J. Cell. Mol. Med. 2024, 28 (4), Art. No: e18132. DOI: 10.1111/JCMM.18132
78. Ordóñez-Vásquez, A.; Jaramillo-Gómez, L.; Duran-Correa, C.; Escamilla-García, E.; Garza-Ramos, M. A. D. la; Suárez-Obando, F. A Reliable and Reproducible Model for Assessing the Effect of Different Concentrations of α-Solanine on Rat Bone Marrow Mesenchymal Stem Cells. Bone Marrow Res. 2017, 2017, Art. No: 2170306. DOI: 10.1155/2017/2170306
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No additional restrictions — You may not apply legal terms or technological measures that legally restrict others from doing anything the license permits.
Notices:
You do not have to comply with the license for elements of the material in the public domain or where your use is permitted by an applicable exception or limitation.
No warranties are given. The license may not give you all of the permissions necessary for your intended use. For example, other rights such as publicity, privacy, or moral rights may limit how you use the material.