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Rezaei, Heresh, Jamshidzadeh, Akram, Arjmand, Abdollah, Abdoli, Narges, Najibi, Asma, Khodaei, Forouzan, Alidaee, Sepideh, Azarpira, Negar, Ommati, Mohammad Mehdi, Heidari, Reza. (1402). Zoledronic Acid-Induced Insulitis in Rats. سامانه مدیریت نشریات علمی, 9(2), 159-168. doi: 10.30476/tips.2023.97995.1181
Heresh Rezaei; Akram Jamshidzadeh; Abdollah Arjmand; Narges Abdoli; Asma Najibi; Forouzan Khodaei; Sepideh Alidaee; Negar Azarpira; Mohammad Mehdi Ommati; Reza Heidari. "Zoledronic Acid-Induced Insulitis in Rats". سامانه مدیریت نشریات علمی, 9, 2, 1402, 159-168. doi: 10.30476/tips.2023.97995.1181
Rezaei, Heresh, Jamshidzadeh, Akram, Arjmand, Abdollah, Abdoli, Narges, Najibi, Asma, Khodaei, Forouzan, Alidaee, Sepideh, Azarpira, Negar, Ommati, Mohammad Mehdi, Heidari, Reza. (1402). 'Zoledronic Acid-Induced Insulitis in Rats', سامانه مدیریت نشریات علمی, 9(2), pp. 159-168. doi: 10.30476/tips.2023.97995.1181
Rezaei, Heresh, Jamshidzadeh, Akram, Arjmand, Abdollah, Abdoli, Narges, Najibi, Asma, Khodaei, Forouzan, Alidaee, Sepideh, Azarpira, Negar, Ommati, Mohammad Mehdi, Heidari, Reza. Zoledronic Acid-Induced Insulitis in Rats. سامانه مدیریت نشریات علمی, 1402; 9(2): 159-168. doi: 10.30476/tips.2023.97995.1181

Zoledronic Acid-Induced Insulitis in Rats

Trends in Pharmaceutical Sciences
مقاله 7، دوره 9، شماره 2، شهریور 2023، صفحه 159-168    اصل مقاله (686.48 K)
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.30476/tips.2023.97995.1181
نویسندگان
Heresh Rezaei1، 2؛ Akram Jamshidzadeh1، 2؛ Abdollah Arjmand3؛ Narges Abdoli4؛ Asma Najibi1، 2؛ Forouzan Khodaei1؛ Sepideh Alidaee1؛ Negar Azarpira5؛ Mohammad Mehdi Ommati1، 6، 7؛ Reza Heidari* 1
1Pharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
2Department of Toxicology and Pharmacology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
3Department of Toxicology and Pharmacology, Faculty of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
4Food and Drug Administration, Iran Ministry of Health and Medical Education, Tehran, Iran.
5Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
6Henan Key Laboratory of Environmental and Animal Product Safety, College of Animal Science and Technology, Henan University of Science and Technology, Luoyang 471000, Henan, China.
7College of Life Sciences, Shanxi Agricultural Sciences, Taigu, Shanxi, China.
چکیده
Insulitis is the inflammation of beta cells of the Langerhans islets. It is well-known that insulitis is a prevalent complication of diabetes. A series of xenobiotics, including drugs, could also induce insulitis. The current study evaluated the effect of zoledronic acid (ZLD) on the pancreas in an animal model. Actually, in an attempt to evaluate the adverse effects of ZLD on the kidney, we noticed severe morphological alterations in the pancreas. Therefore, the effects of ZLD on the pancreas tissue were further investigated. Rats received ZLD (10 and 15 mg/kg, single dose, i.p) and pancreas weight index, serum biomarkers of pancreas injury, the level of pro-inflammatory cytokines (TNF-α, IL-6, and IL-1β), oxidative stress biomarkers in this organ, and pancreas histopathological alterations were assessed. A significant increase in pancreas weight index was detected in ZLD-treated animals. ZLD also significantly increased serum amylase and lipase levels. No significant changes in serum glucose were detected in this study. A significant increase in reactive oxygen species, lipid peroxidation, decreased glutathione levels, and antioxidant capacity was also evident in the pancreas of ZLD-treated rats. Histopathological findings indicate the insulitis lesions of the islets of Langerhans at both doses of 10 and 15 mg/kg of ZLD. The data obtained from this study revealed insulitis as a serious adverse effect associated with high doses of ZLD. Clearly, further studies are warranted to evaluate the effects of other doses and/or patterns of administration of ZLD on pancreas tissue and, finally, the clinical significance of these data.

تازه های تحقیق

Heresh Rezaei (Google Scholar)

Reza Heidari (Google Scholar)

 

کلیدواژه‌ها
Diabetes؛ Glucose metabolism؛ Inflammation؛ Insulitic lesion؛ Oxidative stress
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