Mehdi Nematbakhsh’s research while affiliated with Isfahan University of Medical Sciences and other places

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Publications (11)


Reply to Editor: Serum zinc levels in hemodialysis and peritoneal dialysis patients: A retrospective observational study
  • Article

January 2025

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2 Reads

Journal of Research in Medical Sciences

Mehdi Nematbakhsh

Gender-related diabetic nephropathy: Yes or no
  • Article
  • Full-text available

November 2024

Journal of Research in Medical Sciences

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Baseline hemodynamic data of the mean arterial pressure (MAP) and renal perfusion pressure (RPP) in 8–12-week (a, b) and 24–28-week (c, d) animals in both genders. Data were expressed as the mean ± standard error of the mean. There was no significant difference between males and females in both age categories.
Baseline hemodynamic data of the mean arterial pressure (MAP) and renal perfusion pressure (RPP) in 8–12-week (a, b) and 24–28-week (c, d) animals in both genders. Data were expressed as the mean ± standard error of the mean. There was no significant difference between males and females in both age categories.
Baseline hemodynamic data of the mean arterial pressure (MAP) and renal perfusion pressure (RPP) in 8–12-week (a, b) and 24–28-week (c, d) animals in both genders. Data were expressed as the mean ± standard error of the mean. There was no significant difference between males and females in both age categories.
Figure 3: Hemodynamic data of the mean arterial pressure (MAP) and renal perfusion pressure (RPP) before (base) and after (treat) vehicle or A779 infusion in 8-12-week (a, b) and 24-28-week (c, d) animals in both genders. Data were expressed as the mean ± standard error of the mean. .ere were no signiicant diierences between age-matched males and females receiving vehicle or A779.
Baseline hemodynamic data of the mean arterial pressure (MAP) and renal perfusion pressure (RPP) in 8–12-week (a, b) and 24–28-week (c, d) animals in both genders. Data were expressed as the mean ± standard error of the mean. There was no significant difference between males and females in both age categories.

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Age- and Gender-Related Differences in Renal Vascular Responses to Angiotensin II in Rats: The Role of the Mas Receptor

August 2023

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32 Reads

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1 Citation

Background: Renal hemodynamic is influenced by both gender difference and age. Also, the Mas receptor (MasR) as one of the depressor components of the renin-angiotensin system which has more expression in females could postpone some dysfunctions associated with age, although the association between MasR and age in renal vascular responses to angiotensin II (Ang II) in male and female rats was well undefined. Therefore, the current study examined the effects of age and sex on systemic and renal vascular responses to graded doses of Ang II in Wistar rats with or without MasR antagonists (A779). Materials and methods: Anesthetized Wistar male and female rats with two age ranges of 8-12 and 24-28 weeks were exposed to cannulate venous and arterial vessels. After stability, mean arterial pressure (MAP), renal perfusion pressure (RPP), renal vascular resistance (RVR), and renal blood flow (RBF) were measured in response to the infusion of Ang II with or without A779. Results: There were no significant differences in the base values of MAP, RPP, RBF, and RVR between the two genders in both the age ranges of 8-12 and 24-28 weeks. In addition, no significant gender difference was observed in the age ranges of the above mentioned parameters among the groups receiving vehicle or A779. Also, the infusion of vehicle or A779 could not significantly change the base values. On the other hand, the responses of RBF and RVR to Ang II revealed gender differences among 8-12-week groups (P < 0.05) but not in 24-28-week groups, while the blockade of MasR could not influence the responses in the age ranges. Conclusion: It was concluded that age could impress sex difference in RBF and RVR responses to Ang II infusion and that MasR alone could not participate in these responses. In other words, MasR is not active under normal and acutely elevated Ang II levels.


Sodium hydrogen sulfide may not protect the kidney against ischemia/reperfusion damage in male and female rats

March 2023

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9 Reads

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2 Citations

Research in Pharmaceutical Sciences

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Mehdi Nematbakhsh

Background and purpose: Renal ischemia/reperfusion (IR) injury is a pathologic phenomenon that caused to increase risk of mortality. The main objective of this study was to investigate the effect of sodium hydrogen sulfide (NaHS) on renal IR injury in male and female rats. Experimental approach: Fifty-eight male and female rats were randomized into 4 groups of control, sham, IR, and IR + NaHS. The IR was performed by 45 min of ischemia by vessel clamping followed by 24 h reperfusion. The NaHS (100 µmol/kg) treatment was applied 10 min prior to IR. Finally, after 24 h of reperfusion, the measurements were performed. Findings/results: The serum levels of blood urea nitrogen, creatinine, tissue level of malondialdehyde, and kidney tissue damage score (KTDS) were increased by IR. Urine volume, creatinine, and urea clearances decreased by IR. NaHS administration improved some parameters in males but exacerbated KTDS and serum markers related to renal function. Conclusions and implications: Our data demonstrated that NaHS didn't protect female rats against renal IR injury. In males, it has null effects or just a few protective effects via antioxidant activity.






Angiotensin 1-7 Administration Increases Renal Blood Flow in the Absence of Bradykinin B2 Receptor in Ovariectomized Estradiol Treated Rats: The Role of Mas Receptor

March 2019

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5 Reads

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5 Citations

Acta medica Iranica

Renin angiotensin (RAS), kallikrein kinin (KKS), and sex hormonal systems demonstrate a complex contribution in kidney circulation. This study was designed to investigate the role of angiotensin 1-7 (Ang 1-7) receptor (MasR) and of bradykinin B2 receptor (B2R) in renal blood flow (RBF) response to Ang 1-7 infusion in ovariectomized estradiol treated rats. The ovariectomized rats received intramuscular vehicle (group 1, OV) or estradiol valerate (500 µg/Kg/week) (group 2, OVE) for two weeks. Then each group was divided into two subgroups subjected to receive B2R antagonist (HOE-140, subgroup A), or MasR antagonist (A779) plus HOE-140 (subgroup B). RBF and renal vascular resistance (RVR) responses to graded Ang 1-7 infusion were determined. In condition of B2R alone blocking, RBF response to Ang 1-7 in OVE group was significantly greater than that of OV group (P=0.05), however this response difference was failed by co-blockades of MasR and B2R. Estradiol could promote RBF response to graded Ang 1-7 infusion in the absence of B2R alone, however when both receptors (MasR and B2R) were blocked the role of estradiol was limited. © 2019 Tehran University of Medical Sciences. All rights reserved.



Citations (3)


... In addition, flavonoids also inhibit cyclooxygenase, lipooxygenase, monooxygenase, microsomes, glutathione S-transferase, and NADH oxidase enzymes, all of which are involved in the formation of ROS. When free radicals can be suppressed, oxidative stress does not occur so that plasma MDA levels do not increase, and SOD and CAT enzyme activities do not decrease (21,47). Notably, CPE has an antioxidative role and scavenges doxorubicin-induced oxygen radicals implying one of the main mechanisms in which CPE could protect renal tubular cells against doxorubicin nephrotoxicity. ...

Reference:

The protective effect of hydroalcoholic Citrus aurantifolia peel extract against doxorubicin-induced nephrotoxicity
Sodium hydrogen sulfide may not protect the kidney against ischemia/reperfusion damage in male and female rats
  • Citing Article
  • March 2023

Research in Pharmaceutical Sciences

... The animals anesthetized with urethane (1.7 g/kg dissolved in saline, intraperitoneally) [6] were underwent tracheostomy. After that, the carotid and femoral arteries were isolated. ...

Age- and Gender-Related Differences in Renal Vascular Responses to Angiotensin II in Rats: The Role of the Mas Receptor

... Ang 1-7 is produced from Ang II via angiotensin-converting enzyme 2 (ACE2), the ACE homologue, and binds to a G proteincoupled receptor called MasR [8]. Ang 1-7 contributes to renal physiology and pathology [28,29]. In previous works, we reported the role of this heptapeptide in renal injury and fibrosis [30]. ...

Angiotensin 1-7 Administration Increases Renal Blood Flow in the Absence of Bradykinin B2 Receptor in Ovariectomized Estradiol Treated Rats: The Role of Mas Receptor
  • Citing Article
  • March 2019

Acta medica Iranica