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Original Article

Effects of a triplex mixture of Peganum harmala, Rhus coriaria, and Urtica dioica aqueous extracts on metabolic and histological parameters in diabetic rats

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Pages 1104-1109 | Received 04 May 2014, Accepted 28 Aug 2014, Published online: 23 Jan 2015

Figures & data

Table 1. List of animal groups with different treatments.

Table 2. Summary of the variables and results of ANOVA.

Table 3. Multiple comparison of variables between studied groups of animals using least significance test (LSD).

Figure 1. Microscopic structure of liver of a (a) control rat (group 1) and (b) diabetic rat (group 2) showing marked portal areas, mild piecemeal necrosis, and 1–4 foci per field; (c) PH-treated diabetic rat (group 3) showing moderate portal areas, mild piecemeal necrosis, and 1–4 foci per field; (d) RC-treated diabetic rat (group 4) showing mild portal areas and 1–4 foci per field; (e) UD-treated diabetic rat (group 5) showing moderate portal areas, mild piecemeal necrosis, and 1–4 foci per field; (f) triplex mixture-treated diabetic rat (group 6) showing mild portal areas. All slides stained with hematoxylin and eosin (original magnification ×10).

Figure 1. Microscopic structure of liver of a (a) control rat (group 1) and (b) diabetic rat (group 2) showing marked portal areas, mild piecemeal necrosis, and 1–4 foci per field; (c) PH-treated diabetic rat (group 3) showing moderate portal areas, mild piecemeal necrosis, and 1–4 foci per field; (d) RC-treated diabetic rat (group 4) showing mild portal areas and 1–4 foci per field; (e) UD-treated diabetic rat (group 5) showing moderate portal areas, mild piecemeal necrosis, and 1–4 foci per field; (f) triplex mixture-treated diabetic rat (group 6) showing mild portal areas. All slides stained with hematoxylin and eosin (original magnification ×10).

Figure 2. Microscopic structure of liver of a glibencalmide-treated diabetic rat showing moderate portal areas, mild piecemeal necrosis, and 1–4 foci per field. The slide stained with hematoxylin and eosin (original magnification ×10).

Figure 2. Microscopic structure of liver of a glibencalmide-treated diabetic rat showing moderate portal areas, mild piecemeal necrosis, and 1–4 foci per field. The slide stained with hematoxylin and eosin (original magnification ×10).

Figure 3. Microscopic structure of kidney of a (a) control rat (group 1) and (b) diabetic rat (group 2) showing sever glomerular distension; (c) PH-treated diabetic rat (group 3) showing only a mild glomerular distension; (d) RC-treated diabetic rat (group 4) showing no pathological condition; (e) UD-treated diabetic rat (group 5) showing only a mild glomerular distension; (f) triplex mixture-treated diabetic rat (group 6) showing no pathological condition. All slides stained with hematoxylin and eosin (original magnification ×10).

Figure 3. Microscopic structure of kidney of a (a) control rat (group 1) and (b) diabetic rat (group 2) showing sever glomerular distension; (c) PH-treated diabetic rat (group 3) showing only a mild glomerular distension; (d) RC-treated diabetic rat (group 4) showing no pathological condition; (e) UD-treated diabetic rat (group 5) showing only a mild glomerular distension; (f) triplex mixture-treated diabetic rat (group 6) showing no pathological condition. All slides stained with hematoxylin and eosin (original magnification ×10).

Figure 4. Microscopic structure of kidney of a glibencalmide-treated diabetic rat showing only a mild glomerular distension. The slide stained with hematoxylin and eosin (original magnification ×10).

Figure 4. Microscopic structure of kidney of a glibencalmide-treated diabetic rat showing only a mild glomerular distension. The slide stained with hematoxylin and eosin (original magnification ×10).

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