The role of lutein-rich purple sweet potato leaf extract on the amelioration of diabetic retinopathy in streptozotocin-induced Sprague-Dawley rats
The objective of this study is to access the effect of purple sweet potato leaf (PSPL) extract on diabetic retinopathy (DR) of streptozotocin (STZ)-induced male Sprague-Dawley (SD) rats. In this study, rats were injected intraperitoneally with a single dose of 60 mg/kg STZ, and diabetes was confirme...
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Published in | Frontiers in pharmacology Vol. 14; p. 1175907 |
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Abstract | The objective of this study is to access the effect of purple sweet potato leaf (PSPL) extract on diabetic retinopathy (DR) of streptozotocin (STZ)-induced male Sprague-Dawley (SD) rats. In this study, rats were injected intraperitoneally with a single dose of 60 mg/kg STZ, and diabetes was confirmed on day 7. Rats were further divided into a few groups, which were then orally administered with one of the following treatments: 25 mg/kg of gliclazide (D25G), 200 mg/kg of PSPL extract (DT 200), and 400 mg/kg of PSPL extract (DT 400). However, the normal control (NS) and control group for diabetic (DNS) were given normal saline (NS) for 12 weeks. The results show that the treated group demonstrated a reduction in serum oral glucose tolerance test (OGTT) levels of DT 200 and DT 400, and an increase in the serum and retinal insulin levels, and restored oxidative stress markers in serum and retina on week 12. The PSPL extract exhibited protective effects in maintaining the kidney, liver, retina, and pancreas architecture in 400 mg/kg compared to the 200 mg/kg treated group and D25G, thereby restoring fully transparent lenses in diabetes-induced rats. In conclusion, 400 mg/kg PSPL is the most effective dose for the amelioration of STZ-induced DR pathology in male SD rats. |
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AbstractList | The objective of this study is to access the effect of purple sweet potato leaf (PSPL) extract on diabetic retinopathy (DR) of streptozotocin (STZ)-induced male Sprague–Dawley (SD) rats. In this study, rats were injected intraperitoneally with a single dose of 60 mg/kg STZ, and diabetes was confirmed on day 7. Rats were further divided into a few groups, which were then orally administered with one of the following treatments: 25 mg/kg of gliclazide (D25G), 200 mg/kg of PSPL extract (DT 200), and 400 mg/kg of PSPL extract (DT 400). However, the normal control (NS) and control group for diabetic (DNS) were given normal saline (NS) for 12 weeks. The results show that the treated group demonstrated a reduction in serum oral glucose tolerance test (OGTT) levels of DT 200 and DT 400, and an increase in the serum and retinal insulin levels, and restored oxidative stress markers in serum and retina on week 12. The PSPL extract exhibited protective effects in maintaining the kidney, liver, retina, and pancreas architecture in 400 mg/kg compared to the 200 mg/kg treated group and D25G, thereby restoring fully transparent lenses in diabetes-induced rats. In conclusion, 400 mg/kg PSPL is the most effective dose for the amelioration of STZ-induced DR pathology in male SD rats. |
Author | Embong, Hashim Hussain, Mohd Khairi Othman, Fezah Ahmed, Qamar Uddin Manan, Khairul Aiman Bin Hisamuddin, Ahmad Safiyyu'd-Din Bin Zakaria, Zainul Amiruddin Ismail, Amin Jumidil, Siti Hadizah Naomi, Ruth Bahari, Hasnah |
AuthorAffiliation | 1 Borneo Research on Algesia , Inflammation and Neurodegeneration (BRAIN) Group , Faculty of Medicine and Health Sciences , Sabah Universiti Malaysia , Kota Kinabalu , Sabah , Malaysia 4 Department of Emergency Medicine , Faculty of Medicine , Universiti Kebangsaan Malaysia , Kuala Lumpur , Malaysia 5 Department of Nutrition , Faculty of Medicine and Health Sciences , Universiti Putra Malaysia , Serdang , Malaysia 6 Department of Pharmaceutical Chemistry , Kulliyah of Pharmacy , International Islamic University Malaysia , Kuantan , Pahang , Malaysia 2 Department of Biomedical Sciences , Faculty of Medicine and Health Sciences , Universiti Putra Malaysia , Serdang , Malaysia 3 Department of Human Anatomy , Faculty of Medicine and Health Sciences , Universiti Putra Malaysia , Serdang , Malaysia |
AuthorAffiliation_xml | – name: 4 Department of Emergency Medicine , Faculty of Medicine , Universiti Kebangsaan Malaysia , Kuala Lumpur , Malaysia – name: 6 Department of Pharmaceutical Chemistry , Kulliyah of Pharmacy , International Islamic University Malaysia , Kuantan , Pahang , Malaysia – name: 3 Department of Human Anatomy , Faculty of Medicine and Health Sciences , Universiti Putra Malaysia , Serdang , Malaysia – name: 1 Borneo Research on Algesia , Inflammation and Neurodegeneration (BRAIN) Group , Faculty of Medicine and Health Sciences , Sabah Universiti Malaysia , Kota Kinabalu , Sabah , Malaysia – name: 5 Department of Nutrition , Faculty of Medicine and Health Sciences , Universiti Putra Malaysia , Serdang , Malaysia – name: 2 Department of Biomedical Sciences , Faculty of Medicine and Health Sciences , Universiti Putra Malaysia , Serdang , Malaysia |
Author_xml | – sequence: 1 givenname: Ahmad Safiyyu'd-Din Bin surname: Hisamuddin fullname: Hisamuddin, Ahmad Safiyyu'd-Din Bin organization: Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 2 givenname: Ruth surname: Naomi fullname: Naomi, Ruth organization: Department of Human Anatomy, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 3 givenname: Khairul Aiman Bin surname: Manan fullname: Manan, Khairul Aiman Bin organization: Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 4 givenname: Hasnah surname: Bahari fullname: Bahari, Hasnah organization: Department of Human Anatomy, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 5 givenname: Fezah surname: Othman fullname: Othman, Fezah organization: Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 6 givenname: Hashim surname: Embong fullname: Embong, Hashim organization: Department of Emergency Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia – sequence: 7 givenname: Amin surname: Ismail fullname: Ismail, Amin organization: Department of Nutrition, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 8 givenname: Qamar Uddin surname: Ahmed fullname: Ahmed, Qamar Uddin organization: Department of Pharmaceutical Chemistry, Kulliyah of Pharmacy, International Islamic University Malaysia, Kuantan, Pahang, Malaysia – sequence: 9 givenname: Siti Hadizah surname: Jumidil fullname: Jumidil, Siti Hadizah organization: Department of Human Anatomy, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 10 givenname: Mohd Khairi surname: Hussain fullname: Hussain, Mohd Khairi organization: Department of Biomedical Sciences, Faculty of Medicine and Health Sciences, Universiti Putra Malaysia, Serdang, Malaysia – sequence: 11 givenname: Zainul Amiruddin surname: Zakaria fullname: Zakaria, Zainul Amiruddin organization: Borneo Research on Algesia, Inflammation and Neurodegeneration (BRAIN) Group, Faculty of Medicine and Health Sciences, Sabah Universiti Malaysia, Kota Kinabalu, Sabah, Malaysia |
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Keywords | cataract antioxidants diabetes purple sweet potato retinal changes plant |
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SubjectTerms | antioxidants cataract diabetes Pharmacology plant purple sweet potato retinal changes |
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Title | The role of lutein-rich purple sweet potato leaf extract on the amelioration of diabetic retinopathy in streptozotocin-induced Sprague-Dawley rats |
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