Nithya M, Ragavendran C, Natarajan D. Antibacterial and free radical scavenging activity of a medicinal plant Solanum xanthocarpum. Int J Food Prop. 2018;21(1):313-27.

https://doi.org/10.1080/10942912.2017.1409236

Tekuri SK, Pasupuleti SK, Konidala KK, Amuru SR, Bassaiahgari P, Pabbaraju N. Phytochemical and pharmacological activities of Solanum surattense Burm. f - A review. J Appl Pharm Sci. 2019;9(3):126-36.

https://doi.org/10.7324/JAPS.2019.90318

Pereira APA, Lauretti LBC, Alvarenga VO, Paulino BN, Angolini CFF, Neri-Numa IA, Orlando EA, Pallone JAL, Sant'Ana AS, Pastore GM. Evaluation of fruta-do-lobo (Solanum lycocarpum St. Hill) starch on the growth of probiotic strains. Food Res Int. 2020;133.

https://doi.org/10.1016/j.foodres.2020.109187

Jayakumar K, Murugan K. Solanum alkaloids and their pharmaceutical roles: a review. J Anal Pharm Res. 2016;3(6):397-408.

https://doi.org/10.15406/japlr.2016.03.00075

Moyo SM, Serem JC, Bester MJ, Mavumengwana V, Kayitesi E. The impact of boiling and in vitro human digestion of Solanum nigrum complex (Black nightshade) on phenolic compounds bioactivity and bioaccessibility. Food Res Int. 2020;137:109720.

https://doi.org/10.1016/j.foodres.2020.109720

Akanda RU, Mullahey JJ, Shilling DG. Environmental factors affecting germination of tropical soda apple (Solanum viarum). Weed Sci. 1996;44(3):570-4.

https://doi.org/10.1017/S0043174500094352

Mullahey JJ, Shilling DG, Mislevy P, Akanda R. Invasion of tropical soda apple (Solanum viarum) into the US: lessons learned. Weed Technol. 1998;12(4):733-6

https://doi.org/10.1017/S0890037X00044638

Al Sinani SSS, Eltayeb EA. The steroidal glycoalkaloids solamargine and solasonine in Solanum plants. South African J Bot. 2017;112:253-69.

https://doi.org/10.1016/j.sajb.2017.06.002

Mullahey J. Tropical soda apple (Solanum viarum Dunal), a biological pollutant threatening Florida. Castanea. 1996;61:255-60.

Saha M, Datta BK. Reproductive biology of Solanum viarum Dunal (Solanaceae) in Northeast India. Pleione. 2014;8(2):258-66.

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):266-77.

https://doi.org/10.1016/j.bbamem.2013.08.003

Javed M, Saleem A, Akhtar MF. Diosgenin, a steroidal sapogenin, arrests arthritis through modulation of inflammatory cytokines and oxidative stress biomarkers in Wistar rats. Inflammopharmacology. 2023;31(4):1951-66.

https://doi.org/10.1007/s10787-023-01244-7

Winkiel MJ, Chowański S, Słocińska M. Anticancer activity of glycoalkaloids from Solanum plants: A review. Front Pharmacol. 2022;13:979451.

https://doi.org/10.3389/fphar.2022.979451

Torres-Da Matta J, Kanaan S, Nery da Mata A. Changes in glycolytic metabolism during the regeneration of planarians Dugesia tigrina (Girard). Comp Biochem Physiol Part B Comp Biochem. 1989;93(2):391-6.

https://doi.org/10.1016/0305-0491(89)90097-7

Nery da Matta A, Giovanni De Simone S, Kanaan S, Torres-da Matta J. Aminotransferase activity during the regeneration of planarians Dugesia tigrina (Girard). Comp Biochem Physiol Part B Comp Biochem. 1992;101(3):323-6.

https://doi.org/10.1016/0305-0491(92)90007-E

Knakievicz T, Vieira SM, Erdtmann B, Ferreira HB. Reproductive modes and life cycles of freshwater planarians (Platyhelminthes, Tricladida, Paludicula) from southern Brazil. Invertebr Biol. 2006;125:212-21.

https://doi.org/10.1111/j.1744-7410.2006.00054.x

Tang SZ, Kerry JP, Sheehan D, Buckley DJ. Antioxidative mechanisms of tea catechins in chicken meat systems. Food Chem. 2002;76(1):45-51.

https://doi.org/10.1016/S0308-8146(01)00248-5

Oyaizu M. Studies on Products of Browning Reaction Antioxidative Activities of Products of Browning Reaction Prepared from Glucosamine. Japanese J Nutr Diet. 1986;44(6):307-15.

https://doi.org/10.5264/eiyogakuzashi.44.307

Ted E, McConnell J. A Manual of Psychological Experimentation on Planarians. 1st ed. McConnel J, editor. Ann Arbor, Michigan; 1965. 118 p.

Raffa RB, Valdez JM. Cocaine withdrawal in Planaria. Eur J Pharmacol. 2001;430(1):143-5.

https://doi.org/10.1016/S0014-2999(01)01358-9

Kemp A, Van Heijningen AJ. A colorimetric micro-method for the determination of glycogen in tissues. Biochem J. 1954;56(4):646-8.

https://doi.org/10.1042/bj0560646

Kono Y. Generation of superoxide radical during autoxidation of hydroxylamine and an assay for superoxide dismutase. Arch Biochem Biophys. 1978;186(1):189-95.

https://doi.org/10.1016/0003-9861(78)90479-4

Aebi H. Catalase in vitro. Methods Enzymol. 1984;105:121-6.

https://doi.org/10.1016/S0076-6879(84)05016-3

Ellman GL, Courtney KD, Andres V, Featherstone RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol. 1961;7(2):88-95.

https://doi.org/10.1016/0006-2952(61)90145-9

Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem. 1976;72:248-54.

https://doi.org/10.1016/0003-2697(76)90527-3

Finney DJ. Probit Analysis. J Pharm Sci. 1971;60(9):1432.

https://doi.org/10.1002/jps.2600600940

Rodríguez-Arce E, Saldías M. Antioxidant properties of flavonoid metal complexes and their potential inclusion in the development of novel strategies for the treatment against neurodegenerative diseases. Biomed Pharmacother. 2021;143:112236.

https://doi.org/10.1016/j.biopha.2021.112236

Braguini WL, Pires NV, Alves BB. Phytochemical analysis, antioxidant properties and Brine Shrimp lethality of unripe fruits of Solanum viarum. J Young Pharm. 2018;10(2):159-63.

https://doi.org/10.5530/jyp.2018.10.36

Sarnat HB. Book Review: The First Brain: The Neuroscience of Planarians. J Child Neurol. 2015;30(9):1230-1.

https://doi.org/10.1177/0883073814542952

da Matta AN, Kanaan S, Silva CB, Santos DO, Côrte-Real S, Simone G De, Torres-da-Matta J. Changes in energetic substrates during the regeneration of planarians Dugesia tigrina (Girard). Comp Biochem Physiol Part A Physiol. 1993;105(2):341-5.

https://doi.org/10.1016/0300-9629(93)90218-S

Adeva-Andany MM, González-Lucán M, Donapetry-García C, Fernández-Fernández C, Ameneiros-Rodríguez E. Glycogen metabolism in humans. BBA Clin. 2016;5:85-100.

https://doi.org/10.1016/j.bbacli.2016.02.001

Tokarnia C, Canella C, Döbereiner J. Experimental poisoning by the fruits of Solanum aculeatissimum in cattle. Pesq Agropec Bras. 1973;8:35-9.

Winterbourn CC. Reconciling the chemistry and biology of reactive oxygen species. Nat Chem Biol. 2008;4(5):278-86.

https://doi.org/10.1038/nchembio.85

Halliwell B, Gutteridge JMC. Free Radicals in Biology and Medicine. 5th ed. Oxfor: Oxford Academic Press; 2015.

https://doi.org/10.1093/acprof:oso/9780198717478.001.0001

Chance B, Sies H, Boveris A. Hydroperoxide metabolism in mammalian organs. Physiol Rev. 1979;59(3):527-605.

https://doi.org/10.1152/physrev.1979.59.3.527

Kehrer JP. The Haber-Weiss reaction and mechanisms of toxicity. Toxicology. 2000;149(1):43-50.

https://doi.org/10.1016/S0300-483X(00)00231-6

Valko M, Morris H, Cronin M. Metals, toxicity and oxidative stress. Curr Med Chem. 2005;12(10):1161-208.

https://doi.org/10.2174/0929867053764635

Wang J, Zhang H, Zhang T, Zhang R, Liu R, Chen Y. Molecular mechanism on cadmium-induced activity changes of catalase and superoxide dismutase. Int J Biol Macromol. 2015;77:59-67.

https://doi.org/10.1016/j.ijbiomac.2015.02.037

Wang Y, Branicky R, Noë A, Hekimi S. Superoxide dismutases: Dual roles in controlling ROS damage and regulating ROS signaling. J Cell Biol. 2018;217(6):1915.

https://doi.org/10.1083/jcb.201708007