Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2019 Nov 10;24(22):4069.
doi: 10.3390/molecules24224069.

Effects of Orally Consumed Rosa damascena Mill. Hydrosol on Hematology, Clinical Chemistry, Lens Enzymatic Activity, and Lens Pathology in Streptozotocin-Induced Diabetic Rats

Affiliations

Effects of Orally Consumed Rosa damascena Mill. Hydrosol on Hematology, Clinical Chemistry, Lens Enzymatic Activity, and Lens Pathology in Streptozotocin-Induced Diabetic Rats

İlker Demirbolat et al. Molecules. .

Abstract

Diabetes mellitus is a multisystemic metabolic disorder that may affect the eyes, kidneys, vessels, and heart. Chronic hyperglycemia causes non-enzymatic glycation of proteins and elevation of the polyol pathway resulting in oxidative stress that damages organs. The current study aimed to investigate the dose-dependent effects of orally consumed Rosa damascena Mill. hydrosol on hematology, clinical biochemistry, lens enzymatic activity, and lens pathology in streptozotocin (STZ)-induced diabetic rats. Diabetes was induced into male Sprague-Dawley rats by intraperitoneal administration of STZ (40 mg/kg body weight). Rose hydrosols containing 1515 mg/L and 500 mg/L total volatiles (expressed as citronellol) were introduced to rats orally for 45 days. Consumption of 1515 mg/L volatile containing rose hydrosol successfully ameliorated hematologic, hepatic, and renal functions. Hydrosols also attenuated hyperglycemia and decreased the advanced glycation end-product formation in a dose-dependent manner. Rose hydrosol components significantly increased the lens enzymatic activities of glutathione peroxidase and decreased the activity of aldose reductase to prevent cataractogenesis. Histopathological examinations of rat lenses also indicated that increasing the dose of rose hydrosol had a protective effect on lenses in diabetic conditions. Additionally, in silico modeling of aldose reductase inhibition with rose hydrosol volatiles was carried out for extrapolating the current study to humans. The present results suggest that rose hydrosol exerts significant protective properties in diabetes mellitus and has no toxic effect on all studied systems in healthy test groups.

Keywords: Rosa damascena; aldose reductase; cataract; clinical chemistry; diabetes; hematology; lens pathology; rose hydrosol.

PubMed Disclaimer

Conflict of interest statement

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Figures

Figure 1
Figure 1
Total ion chromatogram of rose hydrosol. 1: 1,8-cineole (internal standard), 2: linalool, 3: 4-terpineol, 4: alpha terpineol, 5: citronellol, 6: nerol, 7: geraniol, 8: 2-phenlyethanol, 9: methyl eugenol, 10: eugenol.
Figure 2
Figure 2
Average water intakes for 45 days.
Figure 3
Figure 3
Microphotographs of lens sections stained with hematoxylin and eosin (HEX100). Panels (1) and (2) indicate the normal lenticular histology of the GR1 and GR2 rats. Panel (3) indicates the slight vacuole formation of the GR4 rats. Panel (4) demonstrates the progressively increasing appearance of vacuoles and homogenized areas in the GR5 rats. Panel (5) shows the loss of the lens capsule and anterior epithelium in the GR3 rats. The scale bar represents 50 µm.
Figure 4
Figure 4
(a) Superposition of human (4QXI) and rat (3O3R) aldose reductase (orange and blue, respectively). (b) Binding positions of NADP+ (black), epalrestat (yellow), citronellol (red), geraniol (green), nerol (orange), linalool (pink), and eugenol (blue) in human aldose reductase.

Similar articles

Cited by

References

    1. American Diabetes Association Diagnosis and classification of diabetes mellitus. Diabetes Care. 2010;33:S62–S69. doi: 10.2337/dc10-S062. - DOI - PMC - PubMed
    1. Pollreisz A., Schmidt-Erfurth U. Diabetic cataract—pathogenesis, epidemiology and treatment. J. Ophthalmol. 2010:2010. doi: 10.1155/2010/608751. - DOI - PMC - PubMed
    1. Nishikawa T., Edelstein D., Du X.L., Yamagishi S., Matsumura T., Kaneda Y., Yorek M.A., Beebe D., Oates P.J., Hammes H.-P. Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage. Nature. 2000;404:787. doi: 10.1038/35008121. - DOI - PubMed
    1. Wolff S.P., Dean R. Glucose autoxidation and protein modification. The potential role of ‘autoxidative glycosylation’in diabetes. Biochem. J. 1987;245:243–250. doi: 10.1042/bj2450243. - DOI - PMC - PubMed
    1. Mullarkey C.J., Edelstein D., Brownlee M. Free radical generation by early glycation products: A mechanism for accelerated atherogenesis in diabetes. Biochem. Biophys. Res. Commun. 1990;173:932–939. doi: 10.1016/S0006-291X(05)80875-7. - DOI - PubMed

MeSH terms

LinkOut - more resources