Artemisia vulgaris Extract as a Novel Therapeutic Approach for Reversing Diabetic Cardiomyopathy in a Rat Model

被引:0
|
作者
Hussain, Ghulam [1 ]
Malik, Abdul [2 ]
Akhtar, Suhail [3 ]
Anwar, Haseeb [1 ]
机构
[1] Govt Coll Univ, Fac Life Sci, Dept Physiol, Faisalabad 38000, Pakistan
[2] King Saud Univ, Coll Pharm, Dept Pharmaceut, Riyadh 11564, Saudi Arabia
[3] AT Still Univ Hlth Sci, Dept Biochem, Kirksville, MO 63501 USA
关键词
Artemisia vulgaris; diabetes; diabetic cardiomyopathy; ECG; P-COUMARIC ACID; HEPATOPROTECTIVE ACTIVITY; BIOLOGICAL-ACTIVITIES; CHLOROGENIC ACID; HYPERTROPHY;
D O I
10.3390/ph17081046
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diabetic cardiomyopathy, a severe diabetic complication, impairs heart function, leading to heart failure. Treatment that effectively addresses this condition without causing side effects is urgently needed. Current anti-hyperglycemic therapies are expensive, has side effects and do not effectively prevent cardiac remodeling. Therefore, it is important to explore natural products that may have the potential to reverse cardiac remodeling. That is why the aim of the current study was to determine the left ventricular remodeling potential of the methanolic extract of Artemisia vulgaris in a diabetic cardiomyopathy rat model. Following the initial comprehensive phytochemical evaluation of plant phenolic and flavonoid content, which showed strong anti-hyperglycemic and antioxidant activities, an extract of Artemisia vulgaris was administered in an in vivo experiment. Diabetic cardiomyopathy was induced in Wistar albino rats according to previously described protocols in the literature, and the effect of treatment was checked by serum and histopathological analysis after 45 days. Artemisia vulgaris treatment significantly (p <= 0.05) reduced fasting blood glucose (108.5 +/- 1.75 mg/dL), glycated hemoglobin (4.03 +/- 0.12 %), serum glucose (116.66 +/- 3.28 mg/dL), insulin (15.66 +/- 0.66 ng/mL), total oxidant status (54.66 +/- 3.22 mu mol H(2)O(2)Equiv.L-1), Malondialdehyde (0.20 +/- 0.01 mmol/L), total cholesterol (91.16 +/- 3.35 mg/dL), triglycerides (130.66 +/- 3.15 mg/dL), low-density lipids (36.57 +/- 1.02 mg/dL), sodium (140 +/- 3.21 mmol/L), calcium (10.44 +/- 0.24 mmol/L), creatine kinase MB (1227.5 +/- 17.89 IU/L), lactate dehydrogenase (1300 +/- 34.64 IU/L), C-reactive protein (30 +/- 0.57 pg/mL), tumor necrosis factor-alpha (58.66 +/- 1.76 pg/mL), atrial natriuretic peptide (2.53 +/- 0.04 pg/mL), B-type natriuretic peptide (10.66 +/- 0.44 pg/mL), aspartate aminotransferase (86.5 +/- 4.99 U/L), Alanine Transaminase (55.33 +/- 2.90 U/L), urea (25.33 +/- 1.15 mg/dL) and creatinine (0.64 +/- 0.02 mg/dL) but significantly increased (p <= 0.05) total antioxidant capacity (1.73 +/- 0.07 mmol Trolox Equil./L), high-density lipids (40 +/- 1.59 mg/dL) and potassium (3.82 +/- 0.04 mmol/L) levels. ECG and histopathology confirmed the significant improvement in remodeling and the reversal of structural changes in the heart and pancreas. In conclusion, Artemisia vulgaris possesses significant left ventricular remodeling potential in course of diabetes-induced cardiomyopathy.
引用
收藏
页数:20
相关论文
共 50 条
  • [11] Preventive Effect of Artemisia capillaris extract on Bone Loss in Ovariectomized Rat Model
    Jang, Hae-Dong
    Lee, Sang-Hyun
    Kim, Young-Ho
    FASEB JOURNAL, 2013, 27
  • [12] Chlorella vulgaris extract and Imiquimod as new therapeutic targets for leishmaniasis: An immunological approach
    de Melo, Maria Gabriella Nunes
    Reino, Isabelle Barreto da Silva Moreira
    Vaitkevicius-Antao, Victor
    da Silva, Jady Moreira
    da Silva Junior, Jose Noe
    de Andrade, Alexsandra Frazao
    Bezerra, Raquel Pedrosa
    Marques, Daniela de Araujo Viana
    da Silva, Silvana de Fatima Ferreira
    de Araujo, Paulo Sergio Ramos
    de Lorena, Virginia Maria Barros
    de Morais, Rayana Carla Silva
    de Paiva-Cavalcanti, Milena
    IMMUNOBIOLOGY, 2024, 229 (01)
  • [13] An Insight into the Pathogenesis of Diabetic Cardiomyopathy Along with the Novel Potential Therapeutic Approaches
    Vig, Himangi
    Ravinandan, A. P.
    Vishwas, Hunsur Nagendra
    Tyagi, Sachin
    Rathore, Shruti
    Wal, Ankita
    Wal, Pranay
    CURRENT DIABETES REVIEWS, 2024, 20 (01)
  • [14] Thioredoxin-Interacting Protein: A Novel Therapeutic Target for Diabetic Cardiomyopathy
    Chen, Junqin
    Cha-Molstad, Hyunjoo
    Shalev, Anath
    DIABETES, 2009, 58 : A208 - A208
  • [15] Diabetes and Chronic Heart Failure: From Diabetic Cardiomyopathy to Therapeutic Approach
    Dei Cas, A.
    Spigoni, V.
    Ridolfi, V.
    Metra, M.
    ENDOCRINE METABOLIC & IMMUNE DISORDERS-DRUG TARGETS, 2013, 13 (01) : 38 - 50
  • [16] Attenuation of diabetic cardiomyopathy by relying on kirenol to suppress inflammation in a diabetic rat model
    Wu, Bin
    Huang, Xue-Yuan
    Li, Le
    Fan, Xiao-Hang
    Li, Peng-Cheng
    Huang, Chuan-Qi
    Xiao, Juan
    Gui, Rong
    Wang, Shun
    JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2019, 23 (11) : 7651 - 7663
  • [17] Diabetic cardiomyopathy: effects of fenofibrate and metformin in an experimental model – the Zucker diabetic rat
    Fabien Forcheron
    Alexandra Basset
    Pauline Abdallah
    Peggy Del Carmine
    Nicolas Gadot
    Michel Beylot
    Cardiovascular Diabetology, 8
  • [18] Diabetic cardiomyopathy: effects of fenofibrate and metformin in an experimental model - the Zucker diabetic rat
    Forcheron, Fabien
    Basset, Alexandra
    Abdallah, Pauline
    Del Carmine, Peggy
    Gadot, Nicolas
    Beylot, Michel
    CARDIOVASCULAR DIABETOLOGY, 2009, 8
  • [19] The role of fibromodulin in myocardial fibrosis in a diabetic cardiomyopathy rat model
    Dai, Xiyan
    Yang, Fan
    Chen, Dongping
    Yang, Lu
    Dong, Zhihui
    Chen, Can
    Xiao, Jianmin
    FEBS OPEN BIO, 2025, 15 (03): : 436 - 446
  • [20] A Novel Bathing Therapeutic Approach for Diabetic Foot Ulcers
    Tappia, Paramjit S.
    Hiebert, Brett
    Sanjanwala, Rohan
    Komenda, Paul
    Sathianathan, Chris
    Arneja, Amarjit S.
    Ramjiawan, Bram
    APPLIED SCIENCES-BASEL, 2021, 11 (18):