| Literature DB >> 32537102 |
Sara Dehyadegari1, Mohammad Mehdi Oloumi2, Shahrzad Azizi3.
Abstract
This study was performed to evaluate the role of electroacupuncture on kidney 1 (Ki1) acupoint to prevent the heart and brain injury following ischemia/reperfusion of both kidneys. 24 Sprague Dawley rats were randomly assigned into four equal groups. In the treatment 1 group, following anesthesia, acupuncture needles were inserted on Ki1 on the palm of both hindlimbs and connected to electroacupuncture unit for a 3.00 Hz direct current, 1 hr before surgery until the end of surgery. In treatment two groups, the electroacupuncture was also performed 48 and 24 hr before the operation, with the same protocol as treatment 1. Control 1 and control 2 groups had the same procedures like the treatment ones, except for acupuncture. Immediately after reperfusion, the samples of brains and hearts were taken and prepared for microscopic examination. Histopathological study of the heart in the control and treatment groups showed the breakage of myofibrils, hyaline necrosis, edema and disorganization of myocytes. The severity of cardiac lesions was decreased in both treatment groups in comparison with the controls. Brain in control and treatment groups showed ischemic necrosis, disorganization of the neurons in the hippocampus, and edema. The severity of lesions was reduced in the treatment groups and showed a significant difference between the control and treatment 1. It could be concluded that electroacupuncture on the Ki1 point could reduce the severity of damages induced by renal ischemia/reperfusion in the remote organs of the heart and brain.Entities:
Keywords: Brain; Electroacupuncture; Heart; Ischemia/reperfusion injury; Kidney
Year: 2020 PMID: 32537102 PMCID: PMC7282218 DOI: 10.30466/vrf.2018.86965.2126
Source DB: PubMed Journal: Vet Res Forum ISSN: 2008-8140 Impact factor: 1.054
Fig. 1A) Normal group: Regular arrangement of cardiomuscular fibers with vesicular nuclei in their center. B) Control 1: Disorganization of cardiac fibers. Interstitial edema and increase in space between the cardiomyocytes, breaking in myofibers, hyaline necrosis (pyknotic nuclei and eosinophilic cytoplasm) (arrow). C) Control 1: Severe hyaline necrosis of cardiac fibers (infarction) (asterisk), normal myocytes with bright pink cytoplasm and vesicular nuclei (arrows). D) Treatment 1: Hyaline necrosis of cells (thin arrows), intercellular edema, and the gap among the myofibers, normal myocytes with clear pink cytoplasm and vesicular nuclei (bold arrows) E) Control 2: Hyaline necrosis of myofibrils on the left side of the figure. F) Treatment 2: Mild necrosis of myocytes, hyalinization of damaged cells (arrows), intercellular edema, and fracture of myofibers (H & E; Figs. 1A, 1B, 1C, 1D, and 1E: Scale bar = 10.00 µm, Fig. 1F: Scale bar = 100 µm)
Evaluation of the average of lesions in different areas of the hippocampus. Data are presented as mean ± SE
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| 135.75 ± 14.23* | 59.00 ± 21.69 | 64.50 ± 7.23* | 259.25 ± 30.59 | 0.03* |
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| 73.33 ± 18.37* | 37.00 ± 18.33 | 20.16 ± 11.58* | 130.50 ± 38.71 | |
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| 119.33 ± 55.47 | 14.00 ± 9.50 | 76.00 ± 30.43 | 209.33 ± 85.69 | 0.29 |
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| 66.40 ± 29.96 | 10.40 ± 5.67 | 46.80 ± 12.59 | 123.60 ± 31.33 | |
* Asterisk indicates a significant difference at p ≤ 0.05.
Fig. 2A) Normal group: The neurons were regular in the hippocampus and had a round, bright, and vesicular nucleus. B) Control 1: Cerebral cortex. Neuronal necrosis with a pyknotic nucleus, and enhanced eosinophilic cytoplasm (arrows). C) Control 1: Severe necrosis of the neurons in the hippocampus and increase the distance between the cells. D) Treatment 1: Neuronal shrinkage with a pyknotic nucleus in the CA1, CA2 and CA3 regions of the hippocampus. E) Control 2: Neuron necrosis in the CA3 region of the hippocampus. F) Treatment 2: Mild necrosis of neurons with pyknotic nuclei and eosinophilic cytoplasm (arrowhead), normal neurons with bright, vesicular nuclei (arrow), (H&E, Figs. 2A, 2C and 2F Scale bar = 10.00 µm, Figs. 2B, 2D and 2E Scale bar = 100µm)