In vivo effects of focused shock waves on tumor tissue visualized by fluorescence staining techniques

• Published in: Bioelectrochemistry (Amsterdam, Netherlands) Vol. 103; pp. 103 - 110
• Main Authors: Lukes, Petr, Zeman, Jan, Horak, Vratislav, Hoffer, Petr, Pouckova, Pavla, Holubova, Monika, Hosseini, S. Hamid R., Akiyama, Hidenori, Sunka, Pavel, Benes, Jiri
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.06.2015
• Subjects: Animals; Apoptosis; Caspase 3 - metabolism; Electric Stimulation Therapy - instrumentation; Electric Stimulation Therapy - methods; Electrical discharge; Eosine Yellowish-(YS); Equipment Design; Fluorescence; Hematoxylin; Immunohistochemistry - methods; In Situ Nick-End Labeling; Male; Necrosis; Neoplasms, Experimental - pathology; Neoplasms, Experimental - therapy; Rats, Inbred Lew; Shock waves; Tumor damage; Shock waves; Electrical discharge; Tumor damage; Necrosis; Apoptosis
• ISSN: 1567-5394; 1878-562X
• DOI: 10.1016/j.bioelechem.2014.08.019

Shock waves can cause significant cytotoxic effects in tumor cells and tissues both in vitro and in vivo. However, understanding the mechanisms of shock wave interaction with tissues is limited. We have studied in vivo effects of focused shock waves induced in the syngeneic sarcoma tumor model using the TUNEL assay, immunohistochemical detection of caspase-3 and hematoxylin–eosin staining. Shock waves were produced by a multichannel pulsed-electrohydraulic discharge generator with a cylindrical ceramic-coated electrode. In tumors treated with shock waves, a large area of damaged tissue was detected which was clearly differentiated from intact tissue. Localization and a cone-shaped region of tissue damage visualized by TUNEL reaction apparently correlated with the conical shape and direction of shock wave propagation determined by high-speed shadowgraphy. A strong TUNEL reaction of nuclei and nucleus fragments in tissue exposed to shock waves suggested apoptosis in this destroyed tumor area. However, specificity of the TUNEL technique to apoptotic cells is ambiguous and other apoptotic markers (caspase-3) that we used in our study did not confirmed this observation. Thus, the generated fragments of nuclei gave rise to a false TUNEL reaction not associated with apoptosis. Mechanical stress from high overpressure shock wave was likely the dominant pathway of tumor damage. [Display omitted] •Shock waves induced extensive but highly localized damage in tumor tissue in vivo.•Cone-shaped area of tumor damage correlated with propagation of conical shock wave.•TUNEL reaction in damaged tumor tissue showed false apoptotic indices.•Mechanical stress effects from shock waves was dominant pathway of tumor damage.