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Research Articles

Early Access

Scientific reports corroborate traditional medical applications aligned with the ‘Doctrine of Signatures' in Southeast Nigeria

DOI
https://doi.org/10.14719/pst.12461
Submitted
29 October 2025
Published
06-07-2026
Versions

Abstract

The Doctrine of Signatures (DOS) is an old tradition that was and is practised throughout the world. Even though often criticised, it describes how people came to know that certain plants have therapeutic uses and/or serve as mnemonic aids for the transfer of such information. Semi-structured questionnaires were issued to 62 informants across the study location and the data obtained were processed and analysed statistically. A total of 73 plants belonging to 34 families were reported to possess signatures that connect them to their medicinal properties. For example, the red colour of extracts from plant parts of Sorghum bicolour, Khaya senegalensis, Justicia secunda, etc., communicates the “signature” and indicates their local use as a blood tonic and for treatment of anaemia. The yellow parts and bitter principles of Morinda lucida, Sphenocentrum jollyanum and Cryptolepis sanguinolenta signify symptoms of yellow fever or malaria and are used to treat such ailments. Plants that have swollen nodes that resemble human joints were reported for the treatment of joint diseases such as rheumatic arthritis. Other examples include plants that are used to treat cancer, inflammation, neurological disorders and organ enlargement. Similarly, poisonous/harmful plants have signatures that suggest their toxicity, such as the presence of certain types of appendages and colour patterns. Most of these claims are backed by already reported scientific results. The knowledge and incorporation of the Doctrine of Signatures is highly practised among the Igbo tribe in Nigeria and could form a reliably informed method for future medicinal plant exploration, communication and development.

References

  1. 1. Nwafor FI, Inya-Agha SI. Ethnobotanical study of indigenous peoples' medicinal plants. In: Egbuna C, Kumar S, Ifemeje JC, Kurhekar JV, editors. Phytochemistry. Vol. 2: Pharmacognosy, nanomedicine and contemporary issues. Canada & USA: Apple Academic Press; 2019. p. 43–68. https://doi.org/10.1201/9780429426193-3
  2. 2. Taylor L. Plant-based drugs and medicines. Carson City (NV): Raintree Nutrition Inc.; 2000.
  3. 3. Singh PG, Farrukhabad UP. Doctrine of Signatures. J East Sci. 2021;14(1):75–95.
  4. 4. Efferth T, Greten HJ. Doctrine of Signatures - mystic heritage or outdated relic from middle aged phytotherapy. J Med Aromat Plant Sci. 2016;5(4):2–3. https://doi.org/10.4172/2167-0412.1000e177
  5. 5. Bradley CB. Doctrine of signatures: An explanation of medicinal plant discovery or dissemination of knowledge. Econ Bot. 2007;61(3):246–55. https://doi.org/10.1663/0013-0001(2007)61[246:DOSAEO]2.0.CO;2
  6. 6. Pearce JM. The doctrine of signatures. Eur Neurol. 2008;15(2):51–52. https://doi.org/10.1159/000131714
  7. 7. Decpu P, Anu P, Shanu P. Is the “doctrine of signatures” signature sequence designed by God? Int J Sci Res Publ. 2016;6(11):568–72.
  8. 8. Bennett BC, Baker MA, Gomez P. Ethnobotany of the Shuar of Eastern Ecuador. Adv Econ Bot. 2002;14:1–299.
  9. 9. Efraim L. Doctrine of signatures in the Medieval and Ottoman Levant. Vesalius. 2002;8(1):13–22.
  10. 10. Dafni A, Efraim L. The doctrine of signatures in present day Israel. Econ Bot. 2002;56(4):328–34. https://doi.org/10.1663/00130001(2002)056[0328:TDOSIP]2.0.CO;2
  11. 11. Aworinde DO, Erinoso SM, Ogundele AA, Teniola OA, Ojo SO. The Doctrine of Signature in herbal prescription in communities of Ondo State, Nigeria. J Med Plants Res. 2018;12(18):222–27. https://doi.org/10.5897/JMPR2018.6576
  12. 12. Nwafor FI, Tchimene MK, Onyekere PF, Nweze NO, Orabueze CI. Ethnobiological study of traditional medicine practices for the treatment of chronic leg ulcer in Southeastern Nigeria. Indian J Tradit Knowl. 2018;17(1):34–42.
  13. 13. Mahomoodally MF, Ramjuttun P. A quantitative ethnobotanical survey of phytocosmetics used in the tropical island of Mauritius. J Ethnopharmacol. 2016;193:45–59. https://doi.org/10.1016/j.jep.2016.07.039
  14. 14. Zhigila DA, Cleophas AB, Sawa FBJ, Abdul SD, Chidiebere C. Plant species diversity, abundance and distribution in communities of Zamfara State, Nigeria: Implications for conservation. Proc NTBA/NSCB Joint B. 2016.
  15. 15. Adaeze J, Dishan E, Tella I. Plant species diversity along River Benue Bank under the influence of siltation and solid waste effluents, Adamawa State, Nigeria. Open Acc Libr J. 2017;4:1–13. https://doi.org/10.4236/oalib.1104125
  16. 16. Kwon-Ndung EH, Akomolafe GF, Goler EE, Terna TP, Ittah MA, Umar ID, et al. Diversity complex of plant species spread in Nasarawa State, Nigeria. Int J Biodivers Conserv. 2016;8(12):334–50.
  17. 17. Odoh UE, Uzor PF, Eze CL, Akunne TC, Onyegbulam CM, Osadebe PO. Medicinal plants used by the people of Nsukka Local Government Area, South-eastern Nigeria for the treatment of malaria: An ethnobotanical survey. J Ethnopharmacol. 2018;218:1–15. https://doi.org/10.1016/j.jep.2018.02.034
  18. 18. Evbuomwan IO, Adeyemi O, Oluba OM. Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: An ethnobotanical study. BMC Complement Med Ther. 2023;23(1):324. https://doi.org/10.1186/s12906-023-04131-4
  19. 19. Kassa Z, Asfaw Z, Demissew S. An ethnobotanical study of medicinal plants in Sheka zone of Southern Nations, Nationalities and Peoples' Regional State, Ethiopia. J Ethnobiol Ethnomed. 2020;16:7. https://doi.org/10.1186/s13002-020-0358-4
  20. 20. Corlett RT. Plant diversity in a changing world: Status, trends and conservation needs. Plant Divers. 2016;38(1):10–16. https://doi.org/10.1016/j.pld.2016.01.001
  21. 21. Chen G, Sun W. The role of botanical gardens in scientific research, conservation and citizen science. Plant Divers. 2018;40(4):181–18. https://doi.org/10.1016/j.pld.2018.07.006
  22. 22. Iwara AI, Gani BS, Njar GN, Deekor TN. Influence of soil physico-chemical properties on the distribution of woody tree/shrub species in South-Southern Nigeria. J Agric Sci. 2011;2(2):69–75. https://doi.org/10.1080/09766898.2011.11884669
  23. 23. Ihenyen J, Mensah JK, Osunde W, Efosa O. Checklist of the tree/shrub species of Edo South, Nigeria. J Appl Environ Biol Sci. 2011;1:276–82.
  24. 24. Bukar SM, Abba HM. Vegetation structure and diversity in Northern Yobe, Nigeria. Asian J Plant Biol. 2022;4(1):36–42. https://doi.org/10.54987/ajpb.v4i1.702
  25. 25. Singh VV, Jain J, Mishra AK. Evaluation of anticonvulsant and antioxidant activity of Senna occidentalis seed extracts. J Drug Deliv Ther. 2019;9(2):183–87. https://doi.org/10.22270/jddt.v9i2.2400
  26. 26. Adebayo AH, John-Africa LB, Agbafor AG, Omotosho OE, Mosaku TO. Anti-nociceptive and anti-inflammatory activities of the extract of Anchomanes difformis in rats. Pak J Pharm Sci. 2014;27(2):265–70.
  27. 27. Agyare C, Boakye YD, Apenteng JA, Dapaah SO, Appiah T, Adow A. Antimicrobial and anti-inflammatory properties of Anchomanes difformis and Colocasia esculenta. Biochem Pharmacol (Los Angel). 2015;5(1):201. https://doi.org/10.4172/2167-0501.1000201
  28. 28. Alabi TD, Chegou NN, Brooks NL, Oguntibeju OO. Effects of Anchomanes difformis on inflammation, apoptosis and organ toxicity in STZ-induced diabetic cardiomyopathy. Biomedicines. 2020;8(2):29. https://doi.org/10.3390/biomedicines8020029
  29. 29. Afolayan FID, Sulaiman KA, Okunade WT. Ethnobotanical survey of plants used in cancer therapy in Iwo and Ibadan, South-Western Nigeria. J Pharm Pharmacogn Res. 2020;8(5):346–67. https://doi.org/10.56499/jppres20.798_8.5.346
  30. 30. Alawode TT, Lajide L, Olaleye MT, Owolabi BJ. Preliminary cytotoxicity studies on some Nigerian medicinal plants used as traditional anticancer remedies. Sci World J. 2021;16(2):94–97.
  31. 31. Asongalem EA, Foyet HS, Ekobo S, Théophile D, Kamtchouing P. Antiinflammatory, lack of central analgesia and antipyretic properties of Acanthus montanus (Ness) T. Anderson. J Ethnopharmacol. 2004;95:63. https://doi.org/10.1016/j.jep.2004.06.014
  32. 32. Okoli CO, Akah PA, Onuoha NJ, Okoye TC, Nwoye AC, Nworu CS. Acanthus montanus: An experimental evaluation of the antimicrobial, anti-inflammatory and immunological properties of a traditional remedy for furuncles. BMC Complement Altern Med. 2008;8:27. https://doi.org/10.1186/1472-6882-8-27
  33. 33. Schippers RR, Bosch CH. Hibiscus asper Hook.f. In: Grubben GJH, Denton OA, editors. PROTA. Wageningen (Netherlands); 2004. http://www.prota4u.org/search.asp
  34. 34. Sri Sainadh N, Nagarathna PKM, Vasantha Kumar C, Kulkarni SC. Evaluation of anti-cancer activity of Kigelia africana on EAC induced breast tumours. J Pharm Pharm Sci. 2013;2(3):78–84.
  35. 35. Dandawate PR, Subramaniam D, Padhaye SB, Anant S. Bitter melon: A panacea for inflammation and cancer. Chin J Nat Med. 2016;14(2):81–100. https://doi.org/10.1016/S1875-5364(16)60002-X
  36. 36. Bortolotti M, Mercatelli D, Polito L. Momordica charantia, a nutraceutical approach for inflammatory-related diseases. Front Pharmacol. 2019;10:486. https://doi.org/10.3389/fphar.2019.00486
  37. 37. Oboh I, Onwukaeme DN. Analgesic, anti-inflammatory and anti-ulcer activities of Sida acuta in mice and rats. Niger J Nat Prod Med. 2005;9:1. https://doi.org/10.4314/njnpm.v9i1.11827
  38. 38. Pieme CA, Penlap VN, Ngogang J, Costache M. In vitro cytotoxicity and antioxidant activities of five medicinal plants of the Malvaceae family from Cameroon. Environ Toxicol Pharmacol. 2010;29:223–28. https://doi.org/10.1016/j.etap.2010.01.003
  39. 39. Mallikarjuna G. Anticancer activity of Sida acuta Burm. f. against nitrosodiethylamine and CCl4-induced hepatocellular carcinoma. Indo Am J Pharm Res. 2013;3(9):74–78.
  40. 40. Cloete L. Diabetes mellitus: An overview of the types, symptoms, complications and management. Nurs Stand. 2022;37(1):61–66. https://doi.org/10.7748/ns.2021.e11709
  41. 41. Tan SY, Wong JL, Sim YJ, Wong SS, Elhassan SA, Tan SH, et al. Type 1 and 2 diabetes mellitus: A review on current treatment approaches and gene therapy as potential intervention. Diabetes Metab Syndr. 2019;13(1):364–72. https://doi.org/10.1016/j.dsx.2018.10.008
  42. 42. Sohanang Nodem FS, Ymele D, Fadimatou M, Fodouop SP. Malaria and typhoid fever coinfection among febrile patients in Ngaoundéré (Adamawa, Cameroon): A cross-sectional study. J Parasitol Res. 2023;2023:5334813. https://doi.org/10.1155/2023/5334813
  43. 43. Happy II, Ezejindu DN, Emmanuel NE. A comparative study on the effect of Vernonia amygdalina (bitter leaf) and glibenclamide in the treatment of diabetes in alloxan-induced diabetic albino Wistar rats.
  44. 44. Ya Nkono BLN, Rouamba A, Duceac IA, Verestiuc L. Antihyperglycemic effect of Vernonia amygdalina and in vitro evaluation of its antiproliferative activity on human osteosarcoma MG-63. Pan Afr Med J. 2022;42:222. https://doi.org/10.11604/pamj.2022.42.222.33149
  45. 45. Michael UA, David BU, Theophine CO, Philip FU, Ogochukwu AM, Benson VA. Antidiabetic effect of combined aqueous leaf extract of Vernonia amygdalina and metformin in rats. J Basic Clin Pharm. 2010;1(3):197–202.
  46. 46. Kazeem MI, Adamson JO, Ogunwande IA. Modes of inhibition of α-amylase and α-glucosidase by aqueous extract of Morinda lucida Benth leaf. Biomed Res Int. 2013;2013:527570. https://doi.org/10.1155/2013/527570
  47. 47. Oladeji OS, Oluyori AP, Dada AO. Antiplasmodial activity of Morinda lucida Benth. leaf and bark extracts against Plasmodium berghei infected mice. Saudi J Biol Sci. 2022;29(4):2475–82. https://doi.org/10.1016/j.sjbs.2021.12.017
  48. 48. Iwu MM, Igboko OA, Okunji CO, Tempesta MS. Antidiabetic and aldose reductase activities of biflavanones of Garcinia kola. J Pharm Pharmacol. 1990;42:290–92. https://doi.org/10.1111/j.2042-7158.1990.tb05412.x
  49. 49. Ogbonna J, Inya-Agha S, Kenechukwu F, Chime S, Attama A, Momoh M. Evaluation of six herbal plants used in the treatment of malaria in South Eastern Nigeria. Int J Pharm Res Biosci. 2013;2(1):148–67.
  50. 50. Teugwa CM, Mejiato PC, Zofou D, Tchinda BT, Boyom FF. Antioxidant and antidiabetic profiles of two African medicinal plants: Picralima nitida (Apocynaceae) and Sonchus oleraceus (Asteraceae). BMC Complement Altern Med. 2013;13:175. https://doi.org/10.1186/1472-6882-13-175
  51. 51. Yessoufou A, Gbenou J, Grissa O, Hichami A, Simonin AM, Tabka Z, et al. Anti-hyperglycemic effects of three medicinal plants in diabetic pregnancy: Modulation of T cell proliferation. BMC Complement Altern Med. 2013;13:77. https://doi.org/10.1186/1472-6882-13-77
  52. 52. François G, Assi LA, Holenz J, Bringmann G. Constituents of Picralima nitida display pronounced inhibitory activities against asexual erythrocytic forms of Plasmodium falciparum in vitro. J Ethnopharmacol. 1996;54:113–17. https://doi.org/10.1016/S0378-8741(96)01456-0
  53. 53. Iwu MM. African medicinal plant in the search for new drugs based on ethnobotanical leads. In: Chadwick DJ, Marsh J, editors. Ethnobotany: Search for new drugs. Ciba Foundation Symposium. Chichester: Wiley; 1994. p. 116–29. https://doi.org/10.1002/9780470514634.ch9
  54. 54. Erharuyi O, Eze AO, Imieje VO, Aghahowa S, Falodun A. Antioxidant and antimalarial activities of methanol extract of Picralima nitida root bark. J Appl Sci Environ Manag. 2023;27(4):727–32. https://doi.org/10.4314/jasem.v27i4.12
  55. 55. Orabueze CI, Adesegun SA, Nwafor FI, Coker HAB. Ethnobotanical survey of medicinal plants and herbal formulations used in the management of malaria in Nsukka, Southeast Nigeria. Niger J Nat Prod Med. 2017;21:66–81.
  56. 56. Atanu FO, Idih FM, Nwonuma CO, Hetta HF, Alamery S, El-Saber Batiha G. Evaluation of antimalarial potential of extracts from Alstonia boonei and Carica papaya in Plasmodium berghei-infected mice. Evid Based Complement Alternat Med. 2021;2021:2599191. https://doi.org/10.1155/2021/2599191
  57. 57. Tudu CK, Bandyopadhyay A, Kumar M. Unravelling the pharmacological properties of cryptolepine and its derivatives: A mini-review insight. Naunyn Schmiedebergs Arch Pharmacol. 2023;396:229–38. https://doi.org/10.1007/s00210-022-02302-7
  58. 58. Ajani EO, Ibrahim LB. Toxicological evaluations of combined administration of ethanolic stem bark extract of Enantia chlorantha and lisinopril in experimental type 2 diabetes. Clin Phytosci. 2020;6:29. https://doi.org/10.1186/s40816-020-00174-z
  59. 59. Burkill HM. Useful plants of West tropical Africa. 2nd ed. Vol. 4 (Families M-R). Kew (England): Royal Botanic Gardens; 1997.
  60. 60. Akanji OC, Cyril-Olutayo CM, Elufioye OT, Ogunsusi OO. The antimalarial effect of Momordica charantia L. and Mirabilis jalapa leaf extracts using an animal model. J Med Plants Res. 2016;10(24):344–50. https://doi.org/10.5897/JMPR2016.6046
  61. 61. Alaribe C, Oladipupo A, Nani M, Ijeoma I, Olanipekun B, Coker H. Suppressive and curative antiplasmodial properties of Nauclea latifolia root extract and fractions against erythrocytic stage of mice-infective chloroquine-sensitive Plasmodium berghei NK-65. J Med Plants Econ Dev. 2020;4(1):6. https://doi.org/10.4102/jomped.v4i1.72
  62. 62. Nkoua Badzi C, Tano Konan D, Dable Marius T. Antiplasmodial activity and acute oral toxicity of Rauvolfia vomitoria leaves extracts. Int J Pharmacol Res. 2018;8(7):56–62.
  63. 63. Olorunnisola OS, Afolayan AJ. In vivo anti-malaria activity of methanolic leaf and root extracts of Sphenocentrum jollyanum Pierre. Afr J Pharm Pharmacol. 2011;5(14):1669–73. https://doi.org/10.5897/AJPP11.117
  64. 64. Goodman CD, Hoang AT, Diallo D, Malterud KE, McFadden GI, Wangensteen H. Anti-plasmodial effects of Zanthoxylum zanthoxyloides. Planta Med. 2019;85(13):1073–79. https://doi.org/10.1055/a-0973-0067
  65. 65. Bolia R. Approach to “upset stomach”. Indian J Pediatr. 2017;84(12):915–21. https://doi.org/10.1007/s12098-017-2376-3
  66. 66. Dicks LMT. How does quorum sensing of intestinal bacteria affect our health and mental status? Microorganisms. 2022;10(10):1969. https://doi.org/10.3390/microorganisms10101969
  67. 67. Henry L, Boue A, Janssen G, Bartlett A. Delayed caecal perforation from amoebic dysentery. ANZ J Surg. 2022;92(6):1522–23. https://doi.org/10.1111/ans.17309
  68. 68. Abdi S, Ataei S, Abroon M, Majma Sanaye P, Abbasinazari M, Farrokhian A. A comprehensive review of the role of complementary and dietary medicines in eradicating Helicobacter pylori. Iran J Pharm Res. 2022;21(1):e127030. https://doi.org/10.5812/ijpr-127030
  69. 69. García MT, Garcia-Vargas JM, Fernández LAG, Cuevas P, Gracia I. Garlic extracts: Effect of pH on inhibition of Helicobacter pylori. Life. 2023;13(7):1434. https://doi.org/10.3390/life13071434
  70. 70. Cellini L, Di Campli E, Masulli M, Di Bartolomeo S, Allocati N. Inhibition of Helicobacter pylori by garlic extract (Allium sativum). FEMS Immunol Med Microbiol. 1996;13(4):273–77. https://doi.org/10.1111/j.1574-695X.1996.tb00251.x
  71. 71. Ross ZM, O'Gara EA, Hill DJ, Sleightholme HV, Maslin DJ. Antimicrobial properties of garlic oil against human enteric bacteria: Evaluation of methodologies and comparisons with garlic oil sulfides and garlic powder. Appl Environ Microbiol. 2001;67:475–80. https://doi.org/10.1128/AEM.67.1.475-480.2001
  72. 72. Cutler R, Wilson P. Antibacterial activity of a new, stable, aqueous extract of allicin against methicillin-resistant Staphylococcus aureus. Br. J Biomed Sci. 2004;61:71–74. https://doi.org/10.1080/09674845.2004.11732646
  73. 73. El-Saber Batiha G, Magdy Beshbishy AG, Wasef L, Elewa YHA, Al-Sagan A, Abd El-Hack ME, et al. Chemical constituents and pharmacological activities of garlic (Allium sativum L.): A review. Nutrients. 2020;12(3):872. https://doi.org/10.3390/nu12030872
  74. 74. Kuete V, Efferth T. Cameroonian medicinal plants: Pharmacology and derived natural products. Front Pharmacol. 2010;1:123. https://doi.org/10.3389/fphar.2010.00123
  75. 75. Iteku JB, Bongo GN, Mbiya JN, Wambale JM, Mutwale PK, Inkoto CL, et al. Phytochemical analysis and evaluation of bioactivities of Cola acuminata extracts. J Biomed Life Sci. 2021;1(1):51–65.https://doi.org/10.31586/jbls.2021.166
  76. 76. Ibu DO, Ibeshi OM, Okpara E. Further identification of the nature of stimulation of gastric acid secretion by Cola nitida using cimetidine and ranitidine. Med Plants Nigeria. 1986;1:7-8.
  77. 77. Abalaka M. Investigation into the medicinal values of Cola species - Cola nitida and Cola acuminata. Sci Agric Bohem. 2015;10(1):31–34. https://doi.org/10.15192/PSCP.SA.2015.10.1.3134
  78. 78. Okudu HO, Asumugha VU, Umoh EJ. Evaluation of the nutrients and phytochemical composition of two varieties of monkey kola membrane (Cola pachycarpa and Cola lepidota). Direct Res J. 2016;4:320–25.
  79. 79. Tona L, Kanbu K, Nigimbi N, Cimanga K, Vietinck AJ. Antiamoebic and phytochemical screening of some Congolese medicinal plants. J Ethnopharmacol. 1999;61(1):57–65. https://doi.org/10.1016/S0378-8741(98)00015-4
  80. 80. Esuoso KO, Odetoun SM. Proximate chemical composition and possible industrial utilisation of Blighia sapida seed and oils. Phytother Res. 2005;72(7):311–13.
  81. 81. Erhirhie EO, Moke GE. Xylopia aethiopica: A review of its ethnomedicinal, chemical and pharmacological properties. Am J PharmTech Res. 2014;4:22–37.
  82. 82. John-Dewole OO, Agunbiade SO, Alao OO, Arojojoye OA. Phytochemical and antimicrobial studies of the extract of the fruit of Xylopia aethiopica for medicinal importance. J Biotechnol Pharm Res. 2012;3(6):118–22.
  83. 83. Mogbojuri OM, Adedapo AA, Abatan MO. Phytochemical screening, safety evaluation, anti-inflammatory and analgesic studies of the leaf extracts of Sterculia tragacantha. J Complement Integr Med. 2016;13(3):221–28. https://doi.org/10.1515/jcim-2015-0114
  84. 84. Udia PM, Braide VP, Owu DU. Antispasmodic and spasmolytic effects of methanolic extract from seeds of Garcinia kola on isolated rat small intestine. Niger J Physiol Sci. 2015;24(2):111–16. https://doi.org/10.4314/njps.v24i2.52912
  85. 85. Gallagher PG. Anaemia in the pediatric patient. Blood. 2022;140(6):571–93. https://doi.org/10.1182/blood.2020006479
  86. 86. Brandow AM, Liem RI. Advances in the diagnosis and treatment of sickle cell disease. J Hematol Oncol. 2022;15(1):20. https://doi.org/10.1186/s13045-022-01237-z
  87. 87. Hoppe C, Neumayr L. Sickle cell disease: Monitoring, current treatment and therapeutics under development. Hematol Oncol Clin North Am. 2019;33(3):355–71. https://doi.org/10.1016/j.hoc.2019.01.014
  88. 88. Verma H. Phytochemical characterisation of twelve medicinal plants used for sickle cell disease management in Chhattisgarh. Int J Pharm Biol Sci. 2015;6:1062–70.
  89. 89. Ekeke G, Shode F. The reversion of sickled cells by Cajanus cajan. Planta Med. 1985;51(6):504–07. https://doi.org/10.1055/s-2007-969576
  90. 90. Kone W, Koffi A, Bomisso E, TraBi F. Ethnomedical study and iron content of anaemia. Afr J Tradit Complement Altern Med. 2011;9:81–87. https://doi.org/10.4314/ajtcam.v9i1.12
  91. 91. Yuan-gang Z, Xiao-lei Y, NanWu Y, Michael W. Chemical composition of the SFE-CO2 extracts from Cajanus cajan (L.) Huth and their antimicrobial activity in vitro and in vivo. Phytomedicine. 2010;17:1095–101. https://doi.org/10.1016/j.phymed.2010.04.005
  92. 92. Khalid MKE, Nora NB, Salma HMAA, Tasbih Elhadi MA, Weam MHA, Wegdan IA, et al. The effect of Cajanus cajan seeds extraction on some haematological parameters among haemorrhagic anaemic rats in Khartoum, Sudan. Biomed J Sci Tech Res. 2020;25(4):ID004220. https://doi.org/10.26717/BJSTR.2020.25.004220
  93. 93. Senou M, Atchadé PT, Dougnon V, Agossadou A, Assogba M, Kinsiclounon E, et al. Efficiency of Sorghum bicolor extract in the treatment of induced anaemia in Wistar rats. Int J Biosci. 2016;8(4):62–71. https://doi.org/10.12692/ijb/8.4.62-71
  94. 94. Ayuba G, Jensen GS, Benson KF, Ademola M, Okubena BA, Okubena O. Clinical efficacy of West African Sorghum bicolour-based traditional herbal preparation Jobelyn shows increased haemoglobin and CD4+ T-lymphocyte counts in HIV+ patients. J Altern Complement Med. 2013;19(25):1–4. https://doi.org/10.1089/acm.2013.0125
  95. 95. Tayo AO, Dosunmu AO, Akinola OI, Adewunmi A, Oloyede OA, Akinbami AA, et al. An open-label randomised parallel-group comparative study of the efficacy of Sorghum bicolour extract in preoperative anaemia. Nutrition. 2016. https://doi.org/10.1016/j.nut.2016.05.005
  96. 96. Hoppe M, Brün B, Larsson MP, Moraeus L, Hulthén L. Heme iron-based dietary intervention for improvement of iron status in young women. Nutrition. 2013;29:89–95. https://doi.org/10.1016/j.nut.2012.04.013
  97. 97. Onyeabo C, Achi NK, Ekeleme-Egedigwe CA, Ebere CU, Okoro CK. Haematological and biochemical studies on Justicia carnea leaves extract in phenylhydrazine-induced anaemia in albino rats. Acta Sci Pol Technol Aliment. 2017;16(2):217–30. https://doi.org/10.17306/J.AFS.2017.0492
  98. 98. Kumar S, Singh P, Mishra G, Srivastav S, Jha K, Khosa RL. Phytopharmacological review of Alternanthera brasiliana (Amaranthaceae). Asian J Plant Sci Res. 2011;1(1):41–47.
  99. 99. Adejumo OE, Owa-Agbanah IS, Kolapo AL, Ayoola MD. Phytochemical and antisickling activities of Entandrophragma utile, Chenopodium ambrosioides and Petiveria alliacea. J Med Plants Res. 2011;5(9):1531–35.
  100. 100. Okokon JE, Antia BS, Udoh AE, Akpan MM. Antianemic and antimicrobial activity of Eremomastax speciosa. J Pharmacol Toxicol. 2007;2(2):196–99. https://doi.org/10.3923/jpt.2007.196.199
  101. 101. Mpiana P, Bokota M, Ndjele M. Antisickling activity of three species of Justicia from Kisangani (D.R. Congo): Justicia tenella, Justicia gendarussa and Justicia insularis. Int J Biol Chem Sci. 2010;4(6):1953–61. https://doi.org/10.4314/ijbcs.v4i6.64984
  102. 102. Oyedapo OA, Cyril-Olutayo CM, Agbedahunsi JM, Adenegan-Alakinde TA, Baderinwa-Adejumo AO. A comparative evaluation of the antisickling, elemental and proximate analysis of the leaves of three Khaya species found in Nigeria. Eur J Med Plants. 2024;35(6):139–49. https://doi.org/10.9734/ejmp/2024/v35i61214
  103. 103. Egunyomi A, Moody JO, Eletu OM. Antisickling activities of two ethnomedicinal plant recipes used for the management of sickle cell anaemia in Ibadan, Nigeria. Afr J Biotechnol. 2009;8(1):20–25.
  104. 104. Ikechukwu EL, Okafor PN, Egba SI. In vitro assessment of the anti-sickling properties of Buchholzia coriacea and Mucuna pruriens seed extracts. In vitro Cell Dev Biol Anim. 2020. https://doi.org/10.1007/s11626-020-00512-y
  105. 105. Roozbeh N, Amirian A, Abdi F, Haghdoost S. A systematic review on the use of medicinal plants for male infertility treatment. J Family Reprod Health. 2021;15(2):74–81. https://doi.org/10.18502/jfrh.v15i2.6447
  106. 106. Akbaribazm M, Goodarzi N, Rahimi M. Female infertility and herbal medicine: An overview of the new findings. Food Sci Nutr. 2021;9(10):5869–82. https://doi.org/10.1002/fsn3.2523
  107. 107. Zhang J, Onakpoya IJ, Posadzki P, Eddouks M. The safety of herbal medicine: From prejudice to evidence. Evid Based Complement Alternat Med. 2015;2015:316706. https://doi.org/10.1155/2015/316706
  108. 108. Sharma A, Jayasena CN, Dhillo WS. Regulation of the hypothalamic-pituitary-testicular axis: Pathophysiology of hypogonadism. Endocrinol Metab Clin North Am. 2022;51(1):29–45. https://doi.org/10.1016/j.ecl.2021.11.010
  109. 109. Okwute P, Oluwatunase G, Mofolorunso A, Asafa O, Ogunbiyi O, Olalekan S. Evaluation of Abrus precatorius on reproductive function of male Wistar rat. Anat J Afr. 2023;12:2384–92. https://doi.org/10.4314/aja.v12i2.6
  110. 110. Hoddinott P, Tappin D, Wright C. Breast feeding. BMJ. 2008;336(7649):881–87. https://doi.org/10.1136/bmj.39521.566296.BE
  111. 111. Dadalto ECV, Rosa EM. Knowledge about the benefits of breastfeeding and the disadvantages of the pacifier related to the mother's practice with preterm infants. Rev Paul Pediatr. 2017;35(4):399–406. https://doi.org/10.1590/1984-0462/;2017;35;4;00005
  112. 112. Penagos TF, Bedoya JJV, Ruiz-Cortes ZT. Pharmacological overview of galactogogues. Vet Med Int. 2014;2014:602894. https://doi.org/10.1155/2014/602894
  113. 113. Bazzano AN, Hofer R, Thibeau S, Gillispie V, Jacobs M, Theall KP. A review of herbal and pharmaceutical galactagogues for breastfeeding. Ochsner J. 2016;16(4):511–24.
  114. 114. Kankara SS, Ibrahim MH, Mustafa M, Go R. Ethnobotanical survey of medicinal plants used for traditional maternal healthcare in Katsina State, Nigeria. S Afr J Bot. 2015;97:165–75. https://doi.org/10.1016/j.sajb.2015.01.007
  115. 115. Omoniwa BP, Longdet IY, Okpatu GC, Oladele KG. Assessment of Gardenia erubescens aqueous root crude extract on male sexual function-related biochemical parameters in clonidine-induced sexual dysfunction Wistar rats. Sci World J. 2022;17(1):83–97.
  116. 116. Maroyi A. Gardenia ternifolia Schum. & Thonn. (Rubiaceae): Review of medicinal uses, phytochemistry and biological activities. Int J Res Pharm Sci. 2020;11(4):5876–85. https://doi.org/10.26452/ijrps.v11i4.3238
  117. 117. Watcho P, Zelefack F, Nguelefack TB, Ngouela S, Telefo PB, Kamtchouing P, et al. Effects of the aqueous and hexane extracts of Mondia whitei on the sexual behaviour and some fertility parameters of sexually inexperienced male rats. Afr J Tradit Complement Altern Med. 2007;4:37–46. https://doi.org/10.4314/ajtcam.v4i1.31190
  118. 118. Martey ONK, He X. Possible mode of action of Mondia whitei: An aphrodisiac used in the management of erectile dysfunction. J Pharmacol Toxicol. 2010;5:460–68. https://doi.org/10.3923/jpt.2010.460.468
  119. 119. Yakubu MT, Oyeyipo TO, Quadri AL, Akanji MA. Effects of aqueous extract of Musa paradisiaca root on testicular function parameters of male rats. J Basic Clin Physiol Pharmacol. 2013;24(2):151–57. https://doi.org/10.1515/jbcpp-2012-0059
  120. 120. Bindu HM, Guddeti V, Praveen TK, Surekha LS, Gayathri M, Allam PV. Evaluation of anti-inflammatory activity of Musa paradisiaca (Linn.)leaves extract in rats. Int J Pharm Chem Biol Sci. 2014;4:753–57.
  121. 121. Onyeto CA, Onwuka AM, Peter IE, Nworu CS, Akah PA. Effect of aqueous extract of unripe Musa paradisiaca Linn. on parameters affecting reproduction in rats. J Evid Based Integr Med. 2024;29:2515690X241249534. https://doi.org/10.1177/2515690X241249534
  122. 122. Raji Y, Fadare OO, Adisa RA, Salami SA. Comprehensive assessment of the effect of Sphenocentrum jollyanum root extract on male reproductive activity in albino rats. Reprod Med Biol. 2006;5:283–92.
  123. 123. Patterson JL, Carapetian SA, Hageman JR, Kelley KR. Febrile seizures. Pediatr Ann. 2013;42(12):249-54. https://doi.org/10.3928/00904481-20131122-09
  124. 124. Manford M. Recent advances in epilepsy. J Neurol. 2017;264(8):1811–24. https://doi.org/10.1007/s00415-017-8394-2
  125. 125. David CV, MacAllister WS. Fine motor impairment in children with epilepsy: Relations with seizure severity and lateralizing value. Epilepsy Behav. 2022;127:108518. https://doi.org/10.1016/j.yebeh.2021.108518
  126. 126. Fine A, Wirrell EC. Seizures in children. Pediatr Rev. 2020;41(7):321–47. https://doi.org/10.1542/pir.2019-0134
  127. 127. Rajapakse T, Buchhalter J. The borderland of migraine and epilepsy in children. Headache. 2016;56(6):1071–80. https://doi.org/10.1111/head.12827
  128. 128. Adjei P, Nkromah K, Akpalu A, Laryea R, Osei Poku F, Ohene S, et al. A cross-sectional comparative study of perceived stigma between patients with epilepsy and patients living with HIV/AIDS in Accra, Ghana. Epilepsy Behav. 2018;89:1–7. https://doi.org/10.1016/j.yebeh.2018.10.015
  129. 129. Al-Snafi A. Therapeutic properties of medicinal plants: A review of medicinal plants with central nervous effects (part 1). Int J Pharmacol Toxicol. 2015;5:177–92.
  130. 130. Fatoba PO, Adeyemi SB, Adewole AA, Fatoba MT. Medicinal plants used in the treatment of infant diseases in Southwestern Nigeria. Niger J Basic Appl Sci. 2018;26(1):14–22. https://doi.org/10.4314/njbas.v26i1.2
  131. 131. Pitchaiah GV, AnilKumar Y, Sravani K. Anxiolytic and anticonvulsant activity of methanolic extract of Allium cepa L. (onion) bulbs in Swiss albino mice. J Pharmacogn Phytochem. 2015;4:131–35.
  132. 132. Advani U, Ansari A, Menghani E. Anticonvulsant potentials of Sesamum indicum and Allium sativum oil alone and in combination in animal models. Int J Pharm Pharm Sci. 2011;3:154–58.
  133. 133. Heryani H, Lestari L. Case study of implementation compresses (Allium cepa L.) to reduce fever in toddlers post DPT immunisation. Genius J. 2023;4(1):207–11. https://doi.org/10.56359/gj.v4i1.85
  134. 134. Yu Y, Yang Z, Jin B, Qin X, Zhu X, Sun J, et al. Cannabidiol inhibits febrile seizures by modulating AMPA receptor kinetics through its interaction with the N-terminal domain of GluA1/GluA2. Pharmacol Res. 2020;161:105128. https://doi.org/10.1016/j.phrs.2020.105128
  135. 135. Ali S, Scheffer IE, Sadleir LG. Efficacy of cannabinoids in paediatric epilepsy. Dev Med Child Neurol. 2019;61(1):13–18. https://doi.org/10.1111/dmcn.14087
  136. 136. Samanta D. Cannabidiol: A review of clinical efficacy and safety in epilepsy. Pediatr Neurol. 2019;96:24–29. https://doi.org/10.1016/j.pediatrneurol.2019.03.014
  137. 137. Elsani M. Evaluation of anti-epileptic activity of ethanolic extract of Lantana camara Linn. in MES and PTZ induced convulsions in rats. Int J Pharm Res Biomed Anal. 2013;2:1–8.
  138. 138. Kazmi I, Gupta G, Afzal M, Anwar F. Anticonvulsant and depressant-like activity of ursolic acid stearoyl glucoside isolated from Lantana camara L. (Verbenaceae). Asian Pac J Trop Dis. 2012;2:S453–S456. https://doi.org/10.1016/S2222-1808(12)60202-3
  139. 139. Worku LA, Bachheti RK, Bisht SS, Bachheti A, Alemu WK. Exploring the medicinal potential of Hyptis suaveolens (Lamiaceae): A comprehensive review of phytochemicals, pharmacological properties and drug development prospects. Nat Prod Commun. 2024;19(11). https://doi.org/10.1177/1934578X241298919
  140. 140. Aderibigbe OA, Iwalewa OA, Adesina KS, Agboola IO. Anxiolytic effect of aridanin isolated from Tetrapleura tetraptera in mice. Int J Pharm Chem Biol Sci. 2010;4(5):1390–96. https://doi.org/10.4314/ijbcs.v4i5.65523
  141. 141. Teitelbaum SL, Bullough PG. The pathophysiology of bone and joint disease. Am J Pathol. 1979;96(1):282–354.
  142. 142. Havelin J, King T. Mechanisms underlying bone and joint pain. Curr Osteoporos Rep. 2018;16(6):763–71. https://doi.org/10.1007/s11914-018-0493-1
  143. 143. Rahmati M, Mobasheri A, Mozafari M. Inflammatory mediators in osteoarthritis: A critical review of the state-of-the-art, current prospects and future challenges. Bone. 2016;85:81–90. https://doi.org/10.1016/j.bone.2016.01.019
  144. 144. Liao Y, Ren Y, Luo X, Mirando AJ, Long JT, Leinroth A, et al. Interleukin-6 signalling mediates cartilage degradation and pain in posttraumatic osteoarthritis in a sex-specific manner. Sci Signal. 2022;15(744):eabn7082. https://doi.org/10.1126/scisignal.abn7082
  145. 145. Cooper MS. Glucocorticoids in bone and joint disease: The good, the bad and the uncertain. Clin Med (Lond). 2012;12(3):261–65. https://doi.org/10.7861/clinmedicine.12-3-261
  146. 146. Anyasor GN, Onajobi F, Osilesi O, Adebawo O, Oboutor EM. Anti-inflammatory and antioxidant activities of Costus afer Ker Gawl. hexane leaf fraction in arthritic rat models. J Ethnopharmacol. 2014;155(1):543–51. https://doi.org/10.1016/j.jep.2014.05.057
  147. 147. Boakye-Gyasi E, Kasanga EA, Biney RP, Abotsi WKM, Mensah KB, Woode E. Ameliorative effects of ethanolic leaf extract of Palisota hirsuta K. Schum (Commelinaceae) on vincristine-induced neuropathic pain in rats. J Appl Pharm Sci. 2014;4(11):35–41.
  148. 148. Sarpong F, Armah F, Amponsah I, Atchoglo P. Antinociceptive ecdysteroids and other constituents of Palisota hirsuta K. Schum (Commelinaceae). J Appl Pharm Sci. 2016;6:147–53. https://doi.org/10.7324/JAPS.2016.601020
  149. 149. Kala C, Ali SS, Abid M, Sharma US, Khan NA. Evaluation of in vivo antiarthritic potential of methanolic extract of Costus speciosus rhizome. J Appl Pharm Sci. 2015;5(8):46–53. https://doi.org/10.7324/JAPS.2015.50808
  150. 150. Irie-N'guessan AG, Kouakou-Siransy NG, Leblais V, Champy P, Kablan BJ. Effet antispasmodique induit par les fractions chromatographiques de trois plantes antiasthmatiques de Côte d'Ivoire. J Pharm Biol Sci. 2010;11:13–20.
  151. 151. Kiki GA, Pop RM, Sabin O, Bocsan IC, Chedea VS, Socaci SA, et al. Polyphenols from Dichrostachys cinerea fruits have anti-inflammatory, analgesic and antioxidant capacity in Freund's adjuvant-induced arthritic rat model. Molecules. 2022;27(17):5445. https://doi.org/10.3390/molecules27175445
  152. 152. Aderibigbe AO, Adeyemi IO, Agboola OI. Central nervous system depressant properties of Treculia africana Decne. Ethnobot Leaflets. 2010;14:108.
  153. 153. Ojimelukwe PC, Ugwuona FU. The traditional and medicinal use of African breadfruit (Treculia africana Decne): An underutilised ethnic food of the Ibo tribe of South East Nigeria. J Ethn Foods. 2021;8:21. https://doi.org/10.1186/s42779-021-00097-1
  154. 154. Dolan LC, Matulka RA, Burdock GA. Naturally occurring food toxins. Toxins. 2010;2(9):2289–332. https://doi.org/10.3390/toxins2092289
  155. 155. Karioti A, Bilia AR. Hypericins as potential leads for new therapeutics. Int J Mol Sci. 2010;11(2):562–94. https://doi.org/10.3390/ijms11020562
  156. 156. Sinmisola A, Oluwasesan BM, Chukwuemeka AP. Blighia sapida K.D. Koenig: A review on its phytochemistry, pharmacological and nutritional properties. J Ethnopharmacol. 2019;235:446–59. https://doi.org/10.1016/j.jep.2019.01.017
  157. 157. Karthikeyan A, Amalnath SD. Abrus precatorius poisoning: A retrospective study of 112 patients. Indian J Crit Care Med. 2017;21(4):224–25. https://doi.org/10.4103/ijccm.IJCCM_320_16
  158. 158. Chandra J, Sandhya S, Ravindran V. Plant toxins: Useful and harmful effects. Hygeia J D Med. 2012;4(4):79–90.

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