Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:

Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5578_Библиотеки_им_академика_М_И_Перельмана

.pdf
Скачиваний:
0
Добавлен:
30.08.2026
Размер:
44 Мб
Скачать
226 Saeideh Momtaz etal.
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
Mohammed, F.I., Al-Essa, M.K., Shafagoj, Y.A. and Afifi, F.U. (2006) Investigation of the direct effects of the
alcoholic extract of Elaeagnus angustifolia L. (Elaeagnaceae) on dispersed intestinal smooth muscle cells of guinea pig. Scientia Pharmaceutica 74(1), 21–30.
Momeni, A., Maghsoodi, H., Rezapour, S., Shiravand, M. and Mardani, M. (2019) Reduction of expression
of IL-18, IL-1β genes in the articular joint by sumac fruit extract (Rhus coriaria L.). Molecular Genetics & Genomic Medicine 7(6), e664.
Momtaz, S., Navabakhsh, M., Bakouee, N., Dehnamaki, M., Rahimifard, M. etal. (2021) Cinnamaldehyde
targets TLR-4 and inflammatory mediators in acetic-acid induced ulcerative colitis model. Biologia 76(6), 1817–1827.
Motevalian, M., Shiri, M., Shiri, S., Shiri, Z. and Shiri, H. (2017) Anti-inflammatory activity of Elaeagnus
angustifolia fruit extract on rat paw edema. Journal of Basic and Clinical Physiology and Pharmacology 28(4), 377–381.
Mueller, D., Triebel, S., Rudakovski, O. and Richling, E. (2013) Influence of triterpenoids present in apple
peel on inflammatory gene expression associated with inflammatory bowel disease (IBD). Food Chemistry 139(1), 339–346.
Mureithi, P.M. (2020) Morphologic and morphometric study on anti-ulcerogenic effects of selected African
nightshades (Solanum nigrum L.) genotypes in the rat. MSc thesis, University of Nairobi, Nairobi.
Naouar, M.S., Mekki, L.Z., Charfi, L., Boubaker, J. and Filali, A. (2016) Preventive and curative effect of
Pistacia lentiscus oil in experimental colitis. Biomedicine & Pharmacotherapy 83, 577–583.
Nascimento, S. and Araruna, C.D.S. (2016) Phytochemicals of Punica granatum L. in inflammatory bowel
diseases: an update. MOL2NET 2(14), 1–x.
Nayebi, N., Khalili, N., Kamalinejad, M. and Emtiazy, M. (2017) A systematic review of the efficacy and
safety of Rosa damascena Mill. with an overview on its phytopharmacological properties. Complementary Therapies in Medicine 34, 129–140.
Nikniaz, Z., Ostadrahimi, A., Mahdavi, R., Ebrahimi, A.A. and Nikniaz, L. (2014) Effects of Elaeagnus an-
gustifolia L. supplementation on serum levels of inflammatory cytokines and matrix metalloproteinases in females with knee osteoarthritis. Complementary Therapies in Medicine 22(5), 864–869.
Pachi, V.K., Mikropoulou, E.V., Gkiouvetidis, P., Siafakas, K., Argyropoulou, A. etal. (2020) Traditional uses,
phytochemistry and pharmacology of Chios mastic gum (Pistacia lentiscus var. Chia, Anacardiaceae): a review. Journal of Ethnopharmacology 254, 112485.
Palla, A.H., Iqbal, N.T., Minhas, K. and Gilani, A.-H. (2016) Flaxseed extract exhibits mucosal protective
effect in acetic acid induced colitis in mice by modulating cytokines, antioxidant and antiinflammatory mechanisms. International Immunopharmacology 38, 153–166.
Palla, A.H., Gilani, A.-U.-H., Bashir, S. and Ur Rehman, N. (2020) Multiple mechanisms of flaxseed:
effectiveness in inflammatory bowel disease. Evidence-Based Complementary and Alternative Medicine 2020, 7974835.
Pandurangan, A.K., Mohebali, N., Norhaizan, M.E. and Looi, C.Y. (2015) Gallic acid attenuates dextran
sulfate sodium-induced experimental colitis in BALB/c mice. Drug Design, Development and Therapy 9, 3923–3934.
Papada, E., Forbes, A., Amerikanou, C., Torović, L., Kalogeropoulos, N. etal. (2018) Antioxidative efficacy
of a Pistacia lentiscus supplement and its effect on the plasma amino acid profile in inflammatory bowel disease: a randomised, double-blind, placebo-controlled trial. Nutrients 10(11), 1779.
Papada, E., Gioxari, A., Amerikanou, C., Forbes, A., Tzavara, C. etal. (2019) Regulation of faecal
biomarkers in inflammatory bowel disease patients treated with oral mastiha (Pistacia lentiscus) supplement: a double-blind and placebo-controlled randomised trial. Phytotherapy Research 33(2), 360–369.
Parisio, C., Lucarini, E., Micheli, L., Toti, A., Khatib, M. et al. (2020) Pomegranate mesocarp against
colitis-induced visceral pain in rats: effects of a decoction and its fractions. International Journal of Molecular Sciences 21(12), 4304.
Pastrelo, M.M., Dias Ribeiro, C.C., Duarte, J.W., Bioago Gollücke, A.P., Artigiani-Neto, R. etal. (2017) Effect
of concentrated apple extract on experimental colitis induced by acetic acid. International Journal of Molecular and Cellular Medicine 6(1), 38–49.
Patlevic, P., Vašková, J., Švorc, P., Vaško, L. and Švorc, P. (2016) Reactive oxygen species and antioxidant
defense in human gastrointestinal diseases. Integrative Medicine Research 5(4), 250–258.
Persic, M., Mikulic-Petkovsek, M., Slatnar, A. and Veberic, R. (2017) Chemical composition of apple fruit,
juice and pomace and the correlation between phenolic content, enzymatic activity and browning. LWT-Food Science and Technology 82, 23–31.
Evidence-Based Review of Medicinal Plant 227
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
Pithadia, A.B. and Jain, S. (2011) Treatment of inflammatory bowel disease (IBD). Pharmacological Reports
63(3), 629–642.
Pituch-Zdanowska, A., Banaszkiewicz, A. and Albrecht, P. (2015) The role of dietary fibre in inflammatory
bowel disease. Przeglad Gastroenterologiczny 10(3), 135–141.
Prachayasittikul, V., Prachayasittikul, S., Ruchirawat, S. and Prachayasittikul, V. (2018) Coriander (Corian-
drum sativum): a promising functional food toward the well-being. Food Research International 105, 305–323.
Putnik, P., Gabric, D., Roohinejad, S., Barba, F.J., Granato, D. etal. (2019) An overview of organosulfur
compounds from Allium spp.: from processing and preservation to evaluation of their bioavailability, antimicrobial, and anti-inflammatory properties. Food Chemistry 276, 680–691.
Qadir, M.I., Ali, M., Saleem, M. and Hanif, M. (2014) Hepatoprotective activity of aqueous methanolic extract
of Viola odorata against paracetamol-induced liver injury in mice. Bangladesh Journal of Pharmacology 9(2), 198–202.
Raeeszadeh, M., Mortazavi, P. and Atashin-Sadafi, R. (2021) The antioxidant, anti-inflammatory, pathological,
and behavioural effects of Medicago sativa L. (alfalfa) extract on brain injury caused by nicotine in male rats. Evidence-Based Complementary and Alternative Medicine 2021, 6694629.
Rafieian-Kopaei, M., Shakiba, A., Sedighi, M. and Bahmani, M. (2017) The analgesic and anti-inflammatory
activity of Linum usitatissimum in Balb/c mice. Journal of Evidence-Based Complementary & Alternative Medicine 22(4), 892–896.
Rahimi, R., Shams-Ardekani, M.R. and Abdollahi, M. (2010) A review of the efficacy of traditional Iranian
medicine for inflammatory bowel disease. World Journal of Gastroenterology 16(36), 4504–4514.
Rahimi, R., Baghaei, A., Baeeri, M., Amin, G., Shams-Ardekani, M.R. etal. (2013) Promising effect of
Magliasa, a traditional Iranian formula, on experimental colitis on the basis of biochemical and cellular findings. World Journal of Gastroenterology 19(12), 1901–1911.
Rai, N., Yadav, S., Verma, A., Tiwari, L. and Sharma, R.K. (2012) A monographic profile on quality specifications
for a herbal drug and spice of commerce – Cuminum cyminum L. International Journal of Advanced Herbal Science and Technology 1(1), 1–12.
Rashidian, A., Akbarzadeh, D., Asgarpanah, J. and Dehpour, A. (2021) Bunium persicum essential oil
reduced acetic acid-induced rat colitis through suppression of NF-κB pathway. Avicenna Journal of Phytomedicine 11(5), 505–514.
Reddy, K.V.K., Maheswaraiah, A. and Naidu, K.A. (2014) Rice bran oil and n-3 fatty acid-rich garden cress
(Lepidium sativum) seed oil attenuate murine model of ulcerative colitis. International Journal of Colorectal Disease 29(2), 267–269.
Riaz, A., Khan, R.A., Afroz, S. and Mallick, N. (2017) Prophylactic and therapeutic effect of Punica granatum
in trinitrobenzene sulfonic acid induced inflammation in rats. Pakistan Journal of Pharmaceutical Sciences 30(1), 155–162.
Rodríguez-Cabezas, M.E., Galvez, J., Lorente, M.D., Concha, A., Camuesco, D. etal. (2002) Dietary fiber
down-regulates colonic tumor necrosis factor α and nitric oxide production in trinitrobenzenesulfonic acid-induced colitic rats. The Journal of Nutrition 132(11), 3263–3271.
Rodríguez-Cabezas, M., Galvez, J., Camuesco, D., Lorente, M., Concha, A. et al. (2003) Intestinal
anti-inflammatory activity of dietary fiber (Plantago ovata seeds) in HLA-B27 transgenic rats. Clinical Nutrition 22(5), 463–471.
Rosenthal, R., Luettig, J., Hering, N., Krug, S., Albrecht, U. etal. (2017) Myrrh exerts barrier-stabilising and
-protective effects in HT-29/B6 and Caco-2 intestinal epithelial cells. International Journal of Colorectal Disease 32(5), 623–634.
Sadar, S.S., Vyawahare, N.S. and Bodhankar, S.L. (2016) Ferulic acid ameliorates TNBS-induced ulcera-
tive colitis through modulation of cytokines, oxidative stress, iNOs, COX-2, and apoptosis in laboratory rats. EXCLI Journal 15, 482–499.
Sajadimajd, S., Bahramsoltani, R., Iranpanah, A., Patra, J.K., Das, G. etal. (2020) Advances on natural
polyphenols as anticancer agents for skin cancer. Pharmacological Research 151, 104584.
Samoila, I., Dinescu, S. and Costache, M. (2020) Interplay between cellular and molecular mechanisms
underlying inflammatory bowel diseases development – a focus on ulcerative colitis. Cells 9(7), 1647.
Sanches-Silva, A., Testai, L., Nabavi, S.F., Battino, M., Devi, K.P. etal. (2020) Therapeutic potential of poly-
phenols in cardiovascular diseases: regulation of mTOR signaling pathway. Pharmacological Research 152, 104626.
Sanei-Dehkordi, A., Vatandoost, H., Abaei, M.R., Davari, B. and Sedaghat, M.M. (2016) Chemical compos-
ition and larvicidal activity of Bunium persicum essential oil against two important mosquitoes vectors. Journal of Essential Oil Bearing Plants 19(2), 349–357.
228 Saeideh Momtaz etal.
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
Sarfraz, R.M., Khan, H., Maheen, S., Afzal, S., Akram, M.R., etal. (2017) Plantago ovata: a comprehensive
review on cultivation, biochemical, pharmaceutical and pharmacological aspects. Acta Poloniae Pharmaceutica 74(3), 739–746.
Sari, D.P., Bellatasie, R. and Ifora, I. (2021) Anti-inflammatory properties of Coriandrum sativum L.: a
review. Research Journal of Pharmacy and Medical Sciences 4(2), 34–38.
Schmidt, C., Grunert, P.C. and Stallmach, A. (2021) An update for pharmacologists on new treatment
options for inflammatory bowel disease: the clinicians’ perspective. Frontiers in Pharmacology 12, 491.
Sendker, J., Böker, I., Lengers, I., Brandt, S., Jose, J. etal. (2017) Phytochemical characterization of low
molecular weight constituents from marshmallow roots (Althaea officinalis) and inhibiting effects of the aqueous extract on human hyaluronidase-1. Journal of Natural Products 80(2), 290–297.
Shah, T.A., Parikh, M., Patel, K.V., Patel, K.G., Joshi, C.G. etal. (2016) Evaluation of the effect of Punica
granatum juice and punicalagin on NFκB modulation in inflammatory bowel disease. Molecular and Cellular Biochemistry 419(1), 65–74.
Shalaby, M.A. and Hammouda, A.A.-E. (2014) Analgesic, anti-inflammatory and anti-hyperlipidemic activities of
Commiphora molmol extract (myrrh). Journal of Intercultural Ethnopharmacology 3(2), 56–62.
Silva, B.M., Andrade, P.B., Ferreres, F., Seabra, R.M., Beatriz, M. etal. (2005) Composition of quince (Cydonia
oblonga Miller) seeds: phenolics, organic acids and free amino acids. Natural Product Research 19(3), 275–281.
Silva, F.G.D. (2016) Antioxidant capacity of protein hydrolysates and phenolic compounds of flaxseed
(Linum usitatissimum L.) and its modulatory effects on experimental colitis. PhD thesis, State University of Campinas, Campinas, Brazil.
Sindhu, G., Ratheesh, M., Shyni, G.L., Nambisan, B. and Helen, A. (2012) Anti-inflammatory and antioxida-
tive effects of mucilage of Trigonella foenum graecum (fenugreek) on adjuvant induced arthritic rats. International Immunopharmacology 12(1), 205–211.
Singh, K., Jaggi, A.S. and Singh, N. (2009) Exploring the ameliorative potential of Punica granatum in dextran
sulfate sodium induced ulcerative colitis in mice. Phytotherapy Research 23(11), 1565–1574.
Singh, S., Kaur, R. and Sharma, S. (2013) Antinociceptive, antiinflammatory and antipyretic activities of
Rumex hastatus D. Don stem and roots. Der Pharmacia Sinica 4(3), 95–102.
Sisay, M. and Gashaw, T. (2017) Ethnobotanical, ethnopharmacological, and phytochemical studies of
Myrtus communis Linn: a popular herb in Unani system of medicine. Journal of Evidence-Based Complementary & Alternative Medicine 22(4), 1035–1043.
Skyberg, J.A., Robison, A., Golden, S., Rollins, M.F., Callis, G. etal. (2011) Apple polyphenols require T
cells to ameliorate dextran sulfate sodium-induced colitis and dampen proinflammatory cytokine expres­sion. Journal of Leukocyte Biology 90(6), 1043–1054.
Solanki, R.P., Gandhi, T.R. and Patel, K.V. (2011) Evaluation of the effect of Quercus infectoria Olivier
(Fagaceae) in experimentally induced inflammatory bowel disease in rats. Research Journal of Pharmacy and Technology 4(5), 782–786.
Sosa, S., Tubaro, A., Della Loggia, R. and Bombardelli, E. (1993) Anti-inflammatory activity of Commiphora
mukul extracts. Pharmacological Research 27, 89–90.
Tabarsa, M., You, S., Yelithao, K., Palanisamy, S., Prabhu, N.M. etal. (2020) Isolation, structural elucidation
and immuno-stimulatory properties of polysaccharides from Cuminum cyminum. Carbohydrate Polymers 230, 115636.
Tafazoli, V., Taherifard, E., Nimrouzi, M. and Pasalar, M. (2022) Therapeutic effect of Plantago major on
active severe pancolitis: a case report. Advances in Integrative Medicine 9, 90–93.
Tafti, L.D., Shariatpanahi, S.M., Damghani, M.M. and Javadi, B. (2017) Traditional Persian topical medica-
tions for gastrointestinal diseases. Iranian Journal of Basic Medical Sciences 20(3), 222–241.
Tang, Y., Li, J., Li, F., Hu, C.-A.A., Liao, P. etal. (2015) Autophagy protects intestinal epithelial cells against
deoxynivalenol toxicity by alleviating oxidative stress via IKK signaling pathway. Free Radical Biology and Medicine 89, 944–951.
Tanideh, N., Afaridi, E., Mehrabani, D., Azarpira, N., Hosseinzadeh, M. etal. (2014) The healing effect of
Berberis vulgaris in acetic acid-induced ulcerative colitis in rat. Middle-East Journal of Scientific Research 21(8), 1288–94.
Tavakoli, A., Shirzad, M., Taghavi, A., Fattahi, M., Ahmadian-Attari, M. etal. (2019) Efficacy of rose oil soft
capsules on clinical outcomes in ulcerative colitis: A pilot randomized, double-blinded, placebo­controlled clinical trial. Galen Medical Journal 8, e1307.
Teimouri, H., Rezaei, M., Abbaszadeh, S. and Azadpour, M. (2019) The effects of aqueous extracts of Cuminum
cyminum L. and Pimpinella anisum L. seeds on the improvement of irritable bowel syndrome compared with loperamide in rats. International Journal of Biology and Chemistry 12(1), 41–47.
Evidence-Based Review of Medicinal Plant 229
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
Wang, Y., Guo, T., Li, J.Y., Zhou, S.Z., Zhao, P. etal. (2013) Four flavonoid glycosides from the pulps of
Elaeagnus angustifolia and their antioxidant activities. Advanced Materials Research 756–759, 16–20.
Weber, L., Kuck, K., Jürgenliemk, G., Heilmann, J., Lipowicz, B. etal. (2020) Anti-inflammatory and barri-
er-stabilising effects of myrrh, coffee charcoal and chamomile flower extract in a co-culture cell model of the intestinal mucosa. Biomolecules 10(7), 1033.
Wei, J., Zhang, X., Bi, Y., Miao, R., Zhang, Z. etal. (2015) Anti-inflammatory effects of cumin essential oil by
blocking JNK, ERK, and NF-κB signaling pathways in LPS-stimulated RAW 264.7 cells. Evidence-Based Complementary and Alternative Medicine 2015, 474509.
Wu, H., Luo, T., Li, Y., Gao, Z., Zhang, K. etal. (2018) Granny Smith apple procyanidin extract upregulates
tight junction protein expression and modulates oxidative stress and inflammation in lipopolysaccha­ride-induced Caco-2 cells. Food & Function 9(6), 3321–3329.
Wu, T.T., Tsai, C.W., Yao, H.T., Lii, C.K., Chen, H.W. etal. (2010) Suppressive effects of extracts from the
aerial part of Coriandrum sativum L. on LPS-induced inflammatory responses in murine RAW 264.7 macrophages. Journal of the Science of Food and Agriculture 90(11), 1846–1854.
Xie, Y., Wang, L., Sun, H., Wang, Y., Yang, Z. et al. (2019) Immunomodulatory, antioxidant and intestinal
morphology-regulating activities of alfalfa polysaccharides in mice. International Journal of Biological Macromolecules 133, 1107–1114.
Yang, K., Zhang, L., Liao, P., Xiao, Z., Zhang, F., Sindaye, D., etal. (2020) Impact of gallic acid on gut health:
Focus on the gut microbiome, immune response, and mechanisms of action. Frontiers in Immunology 16(11), 580208.
Yeganeh, P.R., Leahy, J., Spahis, S., Patey, N., Desjardins, Y. etal. (2018) Apple peel polyphenols reduce
mitochondrial dysfunction in mice with DSS-induced ulcerative colitis. The Journal of Nutritional Biochemistry 57, 56–66.
Yoshioka, Y., Akiyama, H., Nakano, M., Shoji, T., Kanda, T. etal. (2008) Orally administered apple procyanidins
protect against experimental inflammatory bowel disease in mice. International Immunopharmacology 8(13–14), 1802–1807.
Zaghlool, S.S., Shehata, B.A., Abo-Seif, A.A. and Abd El-Latif, H.A. (2015) Protective effects of ginger and
marshmallow extracts on indomethacin-induced peptic ulcer in rats. Journal of Natural Science, Biology, and Medicine 6(2), 421–428.
Zaghlool, S.S., Abo-Seif, A.A., Rabeh, M.A., Abdelmohsen, U.R. and Messiha, B.A. (2019) Gastro-protective
and anti-oxidant potential of Althaea officinalis and Solanum nigrum on pyloric ligation/indomethacin- induced ulceration in rats. Antioxidants 8(11), 512.
Zahouani, Y., Rhouma, K.B., Kacem, K., Sebai, H. and Sakly, M. (2020) Aqueous leaf extract of Pistacia
lentiscus improves acute acetic acid-induced colitis in rats by reducing inflammation and oxidative stress. Journal of Medicinal Food 24(7), 697–708.
Zhang, J.-H., Shangguan, Z.-S., Chen, C., Zhang, H.-J. and Lin, Y. (2016) Anti-inflammatory effects of gug-
gulsterone on murine macrophage by inhibiting LPS-induced inflammatory cytokines in NF-κB signaling pathway. Drug Design, Development and Therapy 10, 1829–1835.
Zhang, Y.-Z. and Li, Y.-Y. (2014) Inflammatory bowel disease: pathogenesis. World Journal of Gastroenter-
ology 20(1), 91–99.
Zhou, H. and Mineshita, S. (2000) The effect of berberine chloride on experimental colitis in rats in vivo and
in vitro. Journal of Pharmacology and Experimental Therapeutics 294(3), 822–829.
Zhou, Q., Ma, L., Zhao, W., Zhao, W., Han, X. etal. (2020) Flaxseed oil alleviates dextran sulphate sodium-
induced ulcerative colitis in rats. Journal of Functional Foods 64, 103602.
Zhu, L., Gu, P. and Shen, H. (2019) Gallic acid improved inflammation via NF-κB pathway in TNBS-induced
ulcerative colitis. International Immunopharmacology 67, 129–137.
Zubair, M., Widén, C., Renvert, S. and Rumpunen, K. (2019) Water and ethanol extracts of Plantago major
leaves show anti-inflammatory activity on oral epithelial cells. Journal of Traditional and Complementary Medicine 9(3), 169–171.
6 Herbal Medicine for Cardiovascular
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
Disease in View of Avicenna
1
Zahra Taghipour1* and Mamak Hashemi Habib Abadi
Department of Traditional Pharmacy, School of Persian Medicine,Tehran University
2
of Medical Sciences,Tehran, Iran; 2Department of Persian Medicine, School of
Medicine, Hamadan University of Medical Sciences, Hamadan, Iran
Abstract
Cardiovascular disease (CVD) is a spectrum of diseases aecting the heart and blood vessels and is the rst cause of death worldwide. e epidemiology of CVD demonstrates a transition, driven by industri alization, urbanization, and associated lifestyle changes, and is taking place in every part of the world among all races, ethnic groups, and cultures. In the present stage, coronary heart disease (CHD), stroke, congestive heart failure, and peripheral vascular disease are the most common CVDs. However, CVDs have historically occurred in the form of rheumatic heart disease and cardiomyopathies due to infection and malnutrition. Avicenna made a great contribution to the eld of cardiology and many of the current well-known concepts can be traced back to his views. He was the rst scientist who established cardi­ology in the early Middle Ages, thus initiating the enormous progress of cardiological sciences up to the present day. Besides nutritional recommendations and specic manipulations (e.g., venesection, hijmat, laxation) to prevent and manage heart diseases, a lot of cardioactive drugs of herbal, animal, and min eral origins are explained by Avicenna to treat dierent heart diseases. In addition, he specically men­tioned 83 simple cardioactive drugs of which 50 are medicinal herbs. In this chapter the medicinal plants used by Avicenna to treat CVDs and new related research studies are presented.
-
-
Cardiovascular disease (CVD) is a spectrum of diseases involving the heart and blood vessels and is the first cause of death glo­bally (Mendis et al., 2015). In 2015, CVDs accounted for ~17.9 million deaths world­wide (32% of total). The epidemiology of CVD demonstrates a transition, driven by industrialization, urbanization, and associ­ated lifestyle changes, and is taking place in every part of the world among all races,
*Email: z_taghipour@ymail.com
230
Introduction
ethnic groups, and cultures. In the present stage, coronary heart disease (CHD), stroke, congestive heart failure, and peripheral vas cular disease are the most common CVDs. However, CVDs have historically occurred in the form of rheumatic heart disease and car­diomyopathies due to infection and malnu­trition (Kasper etal., 2018).
Avicenna made a great contribution to the field of cardiology and many of the cur­rent well-known concepts can be traced back to his views. He was the first scientist who
© CAB International 2023. Medicinal Plants Used in Traditional Persian Medicine
(eds. H. Schulz, Seyed Ahmad Emami and Farsad Nadjafi)
DOI: 10.1079/9781800621671.0006
-
Herbal Medicine for Cardiovascular Disease 231
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
founded cardiology in the Early Middle Ages, thus initiating the enormous progress of cardiological sciences up to the present day (Zarshenas and Zargaran, 2015). He dis­cussed various heart problems in the third book of his comprehensive textbook entitled The Canon of Medicine (Al-Qanun fi’l-Tibb) (Ibn Sinā, 2002; Sobhani et al., 2017) as well as in another specific book named The Trea- tise on Cardiac Drugs (Al-Adwiyah al-Qalbiyah) (Ibn Sinā, 2009). According to the era when Avicenna wrote his books, CHD was not the most common CVD, so as we see, he re­ported heart diseases similar to myocarditis and some disorders of rhythm and myocar­dial infarction.
Besides nutritional recommendations and specific manipulations (e.g., venesection, hijmat, laxation) to prevent and manage heart diseases, a lot of cardioactive drugs of herbal, animal, and mineral origins are explained by Avicenna to treat different heart diseases. In addition, he specifically mentioned 83 simple cardioactive drugs of which 50 are medicinal herbs (Sobhani etal., 2017).
Cardiovascular Diseases
and Treatments in View of Avicenna
cold cardiac dystemperament is treated
with warm-temperament foods, moder­ate exercise, wine, oral complex drugs (maʿajoon), and topical warming liquid and semiliquid drugs on the chest;
dry cardiac dystemperament is treated
by drinking cool water, decreasing activ­ity, taking a bath afterward eating, therapeutic sitz baths, and moisturizing foods and drugs; and
wet cardiac dystemperament is treated
with frequent exercises, taking a bath before eating, and administering laxa­tive and diuretics.
It seems that heart dystemperaments are some kinds of myocarditis from the conven­tional medicine point of view.
Heart warm inflammation (waram har )
This can be a fatal disease that manifests with severe palpitation (khafaqān) plus symptoms of heat and inflammation in the heart. In most cases venesection is necessary and lifesaving, then local administration of herbal lotions and continued drinking of cool liquid drugs. This condition resembles acute infectious myocarditis.
According to the concepts of Traditional Per­sian Medicine (TPM), the heart is the origin of the “innate body heat” and so the factors affecting “innate body heat” may lead to car­diac weakness and diseases. Excess in exer­cise and sexual activity, emotional stress, and insomnia are the most important men­tioned factors.
Heart dystemperaments
In accordance with humoral medicine, treat­ments for cardiac disorders that can lead to various clinical symptoms are divided into the following four types:
warm cardiac dystemperament is treat-
ed with specic fruit sauces like apple
and quince and topical cooling liquid
and semiliquid drugs on the chest;
Syncope (al-ghashi)
Syncope may be caused by suppression of body motor functions due to heart weakness. Weakness in other headship organs like the brain and liver, or in related organs such as the stomach, can also lead to heart weakness and finally cause fainting (al-ghashi). Multiple fac­tors are listed as its etiology such as obstruc­tion, inflammations, enormous discharges, severe pains, and emotional disasters.
Sudden force decrease
(soqut-al-qowah)
This condition is similar to al-ghashi but dif­ferent in etiology and intensity. In this condi­tion patients do not drop and can move even with excessive effort. Hence soqūt-al-qowah
232 Zahra Taghipour and Mamak Hashemi Habib Abadi
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
may lead to al-ghashi (syncope) if it intensi­fies. The cause is excessive dense humors.
Palpitation (khafaqan)
Palpitation (khafaqān) is considered fascicula­tion (abnormal movement) triggered in the heart. Its etiology is any factor that disturbs the heart or pericardium, either a somatic fac­tor or a psychological one, such as severe anx­iety. It is an irregular pulse, characterized by changeable intensity, frequency, and speed.
Myocardial infarction (mawt e faj’ah)
The increase in blood viscosity and appear­ance of clots may lead to arterial obstruction in the heart and cause myocardial infarction (mawt e fajʼah). Regarding the basics of TPM, Avicenna explained that yellow bile is needed to restore permeability in the capillaries and arteries. In the case of a decrease in yellow bile, he emphasized, blood viscosity could lead to arterial obstruction and myocardial infarction.
automaticity, and triggered activity are pro­posed mechanism for arrhythmia (Lévy and Olshansky, 2021).
Treatment
Some rhythm disturbances, such as rapid rates in atrial fibrillation, or sustained ven­tricular tachycardia, require urgent atten­tion. Others, such as ectopic atrial and ven­tricular beats, may cause concern but do not need immediate management. Depending on the individual patient’s situation, antiar­rhythmic drugs, pacemakers, implantable cardioverter-defibrillators (ICDs), and biven­tricular devices may be prescribed (Lévy and Olshansky, 2021).
Shock
Shock is defined as a state of cellular and tis­sue hypoxia that can be due to intracardiac causes of cardiac pump failure that result in reduced cardiac output (CO). Myocardial in­farction, atrial and ventricular tachyar­rhythmias, and bradyarrhythmias as well as mechanical disturbance can lead to shock (Gaieski and Mikkelsen, 2021).
Brief Review on Some Types of
Cardiovascular Diseases and Their
Treatments in Modern Medicine
An arrhythmia is any rhythm that is not a normal sinus rhythm with normal atrioven­tricular (AV) conduction, of which palpita­tion is its most common presentation. This disorder can occur as bradycardias, ventricu­lar tachycardia, atrial fibrillation, AV block, etc. Palpitation, which is defined as an un­pleasant awareness of the forceful, rapid, or irregular beating of the heart, is one of the disorders induced by arrhythmia. Abnormal impulse formation can arise from abnormal automaticity or triggered activity originating from the sinoatrial (SA) node or other sites. Hypoxia, ischemia, or excess catecholamine activity could lead to abnormal automati­city. Ion channels and currents, enhanced
Arrhythmia
Treatment
Ventilatory support followed by hemo­dynamic support with/without norepineph­rine, dopamine, and nitroglycerin, etc. can be prescribed depending on the patient’s condition (Gaieski and Mikkelsen, 2021).
Scientifc Evaluation of Medicinal
Plants Mentioned for the Management
of Cardiovascular Diseases
in Avicenna’s Canon
The medicinal herbs mentioned in the Canon of Medicine for the management of CVDs
and some scientific evidence supporting their efficacy are described individually in this section. In addition, the traditional ap­plication of some plants is also reported. All collected results are presented in Tables 6.1,
6.2, 6.3, and 6.4.
Table 6.1. Medicinal plants mentioned in Canon of Medicine for treatment of CVD.
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
Common English
No. Scientific name(s) Synonym(s) Arabic name(s)
1 Anchusa azurea Mill.
Echium amoenum Fisch. & C.A. Mey. 2 Doronicum grandiflorum Lam. Doronicum scorpioides Lam. Dorunaj Asteraceae 3 Zingiber zerumbet (L.) Sm. Amomum zerumbet L. Zurunbad Bitter ginger Zingiberaceae 4 Crocus sativus L. Crocus officinalis (L.) Honck. Zaʿ afaran Saffron Iridaceae 5 Curcuma zedoaria (Christm.) Roscoe Costus nigricans Blanco Jadwar White turmeric Zingiberaceae 6 Centaurea behen L. Centaurea alata Lam. Bahman abyad White behen Asteraceae 7 Limonium vulgare Mill. Statice limonium L. Bahman ahmar Sea lavender Plumbaginaceae 8 Syzygium aromaticum (L.) Merr. & L.M.
Perry
9 Melissa officinalis L. Melissa hirsuta Hornem. Badranjbuyah,
10 Ocimum basilicum L. Ocimum album L. Badruj Basil Lamiaceae (Labiatae) 11 Tanacetum balsamita L. Balsamita major Desf. Shahesfaram Balsam weed Asteraceae 12 Amomum subulatum Roxb. Cardamomum subulatum (Roxb.) Kuntze Qaqolah, Hil aswad Black cardamom Zingiberaceae 13 Piper cubeba L. Cubeba officinalis Rafin. Kababah Cubeb Piperaceae 14 Clinopodium acinos (L.) Kuntze Calamintha acinos (L.) Clairv. Falanjmeshk Basil thyme Lamiaceae (Labiatae) 15 Citrus medica L. Citrus × aurantium var. medica (L.)
16 Cinnamomum citriodorum Thwaites Camphora citriodora (Thwaites) Lukman. Sadaj hendi Malabar cinnamon Lauraceae 17 Inula helenium L. Aster helenium Scop. Rasan Elecampane Asteraceae 18 Cinnamomum camphora (L.) J. Presl. Camphora camphora (L.) H. Karst. Kafur Camphor Lauraceae 19 Pterocarpus santalinus L. Lingoum santalinum (L.f.) Kuntze Sandal ahmar Red sandalwood Fabaceae (Leguminosae) 20 Santalum album L. Sirium myrtifolium L. Sandal abyad White sandalwood Fabaceae (Leguminosae) 21 Rosa × damascena Mill. Rosa belgica Mill. Ward juri Damask rose Rosaceae 22 Bambusa bambos (L.) Voss B
23 Malus domestica Borkh. Pyrus malus L. To f fa h Apple Rosaceae 24 Coriandrum sativum L. Coriandrum majus Gouan Kozbarah Coriander Apiaceae (Umbelliferae) 25 Raphanus sativus L. Raphanus candidus Vorosch. Fojl Radish Brassicaceae (Cruciferae) 26 Citrullus colocynthis (L.) Schrad. Cucumis colocynthis L. Hanzal Bitter apple Cucurbitaceae
Echium orientale C.A. Mey. Anchusa italica Retz.
Caryophyllus aromaticus L. Qaranful Clove Myrtaceae
Wight & Arn.
ambusa arundinacea (Retz.) Willde.
Gavzaban Bugloss
Toranjan
Otroj Citron Rutaceae
Kheizaran, Tabashir Giant thorny
name Family
Boraginaceae
Sea bugloss
Lemon balm Lamiaceae (Labiatae)
Poaceae (Gramineae)
bamboo
Continued
Herbal Medicine for Cardiovascular Disease 233
Common English
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
No. Scientific name(s) Synonym(s) Arabic name(s) name Family
27 Laricifomes officinalis (Vill.)
Kotl. & Pouzar 28 Cuscuta epithymum Murray Cuscuta acutiflora Rota Aftimoon Dodder Convolvulaceae 29 Cydonia oblonga Mill. Safarjal Quince Rosaceae 30 Pyrus communis L. Komathara Common pear Rosaceae 31 Origanum majorana L. Majorana hortensis Moench Marzanjosh Sweet marjoram Lamiaceae (Labiatae) 32 Moringa oleifera Lam. Hyperanthera moringa (L.) Vahl . Ban Ben Moringaceae 33 Hordeum vulgare L. Hordeum sativum Pers. Shaʿir Common barley Poaceae (Gramineae) 34 Punica granatum L. Punica nana L. Romman (jolnar) Pomegranate Lythraceae 35 Amaranthus blitum L. Amaranthus alius K. Krause Baqlah yamaniah Blite Amaranthaceae 36 Salix sp. Khalaf Willow Salicaceae 37 Citrus limon (L.) Burm.f. Laymun Lemon Rutaceae 38 Rheum palmatum L. Rheum potaninii Losinsk. Rawand Rhubarb Polygonaceae 39 Lens culinaris Medik. Ervum lens Wall. Aʿdas Lentil Fabaceae (Leguminosae) 40 Aquilaria agallocha Roxb. Uʿd Eaglewood Thymelaeaceae 41 Alhagi maurorum Medik. Alhagi camelorum Fisch. Taranjebin, Aʿqul Manna of
42 Lactuca sativa L. Lactuca palmata Willd. Khas Lettuce Asteraceae 43 Cichorium intybus L.
Cichorium endivia L.
44 Portulaca oleracea L. Portulaca fosbergii Poelln. Baqlat al hamqa Common purslane Portulacaceae 45 Atropa belladonna L. Atropa lethalis Salisb. Lifah Belladonna Solanaceae 46 Papaver somniferum L. Al’afiun Opium poppy Papaveraceae 47 Operculina turpethum (L.) Silva Manso Ipomoea turpethum (L.) R. Br. Torbod Turbith Convolvulaceae 48 Commiphora mukul (Hook. ex Stocks)
Engl. 49 Terminalia chebula Willd. ex Flem. Terminalia gangetica Roxb. Ihlilaj kabuli Chebulic
50 Cicer arietinum L. Cicer album Hort. Himmas Chickpea Fabaceae (Leguminosae) 51 Cucumis sativus L. Cucumis esculentus Salisb. Khiar Cucumber Cucurbitaceae 52 Boswellia sacra Flueck. Boswellia carteri Birdw. Kondor Frankincense Burseraceae 53 Myrtus communis L. Myrtus acuta Mill. As Myrtle Myrtaceae
Fomitopsis officinalis (Vill.) Fr.
Bond. & Sing.
Cichorium commune Pall. Cichorium ambiguum Schult.
Balsamodendrum mukul Hook.
ex Stocks
Gharighun Ghariqun Fomitopsidaceae
Fabaceae (Leguminosae)
hedysarum
Hindiba’ Chicory Asteraceae
Endive
Muqil Guggul Burseraceae
Combretaceae
myrobalan
234 Zahra Taghipour and Mamak Hashemi Habib Abadi
54 Paeonia officinalis L. Moutan officinalis (L.) Lindl. & Paxton Fawania Common peony Paeoniaceae
Downloaded from https://cabidigitallibrary.org by Ivanov Ivan, on 11/04/24.
Subject to the CABI Digital Library Terms & Conditions, available at https://cabidigitallibrary.org/terms-and-conditions
https://t.me/med1917
55 Hyssopus officinalis L. Thymus hyssopus E.H.L. Krause Zufa Hyssop Lamiaceae (Labiatae) 56 Nardostachys jatamansi (D. Don) DC. Nardostachys grandiflora DC. Naridin, Sonbol
Hindi
57 Sinapis alba L. Brassica hirta Moench Khardal abyad White mustard Brassicaceae 58 Brassica nigra (L.) K. Koch Sinapis nigra L. Khardal aswad Black mustard Brassicaceae 59 Anacyclus pyrethrum (L.) Lag. Anthemis pyrethrum L. Aʿqraqarha Pellitory Asteraceae 60 Pistacia lentiscus L. Lentiscus vulgaris Fourr. Mistakiu Mastic Anacardiaceae 61 Lilium candidum L. Lilium album Houtt. Susan azad Madonna lily Liliaceae 62 Commiphora myrrha (Nees) Engl. Balsamodendrum myrrha T. Nees Mor Myrrh Burseraceae
Commiphora habessinica
(O. Berg) Engl.
Commiphora schimperi
(O. Bergman) Engl. 63 Convolvulus scammonia L. Saqmunia Scammony Convolvulaceae 64 Olea europaea subsp. cuspidata
(Wall. & G. Don) Cif.
Olea europaea L. Olea pallida Salisb.
65 Prunus amygdalus Stokes Lawz Almond Rosaceae
Commiphora abyssinica (Engl.) Engl.
Balsamea schimperi Engl.
Olea africana Mill. Zaytun Olive Oleaceae
Nard Caprifoliaceae
Herbal Medicine for Cardiovascular Disease 235