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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 28, No 6, November/December 2017

392

AFRICA

the MI group (Fig. 2E) had statistically significantly reduced

irisin immunoreactivity (

p

<

0.05). Relative to the MI group, MI

+

ILO (Fig. 2F), MI

+

SIL (Fig. 2G) and MI

+

ILO

+

SIL (Fig.

2H) all showed elevated irisin immunoreactivity, similar to that

of the control group.

Irisin immunoreactivity (black arrow) was also observed

in the hepatocytes of the liver tissue in all groups. Irisin

immunoreactivity was similar in the control (Fig. 3A), ILO

(Fig. 3B), SIL (Fig. 3C) and ILO

+

SIL (Fig. 3D) groups.

However, relative to the control group, the MI group had

statistically significantly reduced irisin immunoreactivity (

p

<

0.05), while the MI

+

ILO (Fig. 3F), MI

+

SIL (Fig. 3G) and MI

+

ILO

+

SIL (Fig. 3H) groups had significantly increased irisin

immunoreactivity, similar to that in the control group.

Examination

under

the

light

microscope

of

immunohistochemical staining to detect irisin immunoreactivity

showed that the tubule cells in the renal cortex of the kidney

of all groups had irisin immunoreactivity (black arrow). Irisin

immunoreactivity was similar in the control (Fig 4A), ILO

(Fig. 4B), SIL (Fig. 4C) and ILO

+

SIL (Fig. 4D) groups. In

comparison with the control group, the MI (Fig. 4E) group had

a statistically significant decrease in irisin immunoreactivity

(

p

<

0.05). However, the MI

+

ILO (Fig. 4F), MI

+

SIL (Fig.

4G), MI

+

ILO

+

SIL (Fig. 4H) had a significantly higher irisin

immunoreactivity. Table 2 summarises the histological scores of

irisin immunoreactivity in all tissues and groups.

When serum irisin levels in the ischaemic group were

compared to those of the control group, they were found to be

significantly lower than the controls. However, the groups to

which ILO and SIL were administered, either individually or in

combination, had elevated serum irisin levels. Serum irisin levels

of the control group and the groups administered ILO and SIL

before MI induction were statistically similar.

Table 1. Histological scores in the heart tissue of rats

with induced cardiac ischaemia

Inflamma-

tory cells Congestion Fibrosis Oedema

Tissue

integrity Necrosis

Control

0 ± 00

0 ± 00 0 ± 00 0 ± 00

0 ± 00 0 ± 00

MI

2.33 ± 0.51

a

2.50 ± 0.83

a

0 ± 00 3.16 ± 0.40

a

2.83 ± 0.98

a

0 ± 00

MI: myocardial ischaemia–reperfusion;

a

In comparison with the control group,

p

<

0.05.

Fig. 3.

Irisin immunoreactivity after iloprost (ILO) and sildenafil (SIL) administration to hepatic tissues with cardiac ischaemia.

Control (A), ILO (B), SIL (C), ILO

+

SIL (D), MI

+

ILO (F), MI

+

SIL (G), MI

+

ILO

+

SIL (H) and negative control; no irisin

immunoreactivity (I).

A

D

G

B

E

H

C

F

I