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- Erratum (January 2014)
Sound preconditioning therapy inhibits ototoxic hearing loss in mice
Soumen Roy, Matthew M. Ryals, Astrid Botty Van den Bruele, Tracy S. Fitzgerald, and Lisa L. Cunningham
National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Rockville, Maryland, USA.
Address correspondence to: Lisa L. Cunningham, National Institute on Deafness and Other Communication Disorders, NIH, 5 Research Ct., Rockville, Maryland 20850, USA. Phone: 301.443.2766; Fax: 301.402.7580; E-mail: Lisa.cunningham@nih.gov.
Authorship note: Soumen Roy and Matthew M. Ryals are co–senior authors and contributed equally to this work.
Find articles by Roy, S. in: JCI | PubMed | Google Scholar
National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Rockville, Maryland, USA.
Address correspondence to: Lisa L. Cunningham, National Institute on Deafness and Other Communication Disorders, NIH, 5 Research Ct., Rockville, Maryland 20850, USA. Phone: 301.443.2766; Fax: 301.402.7580; E-mail: Lisa.cunningham@nih.gov.
Authorship note: Soumen Roy and Matthew M. Ryals are co–senior authors and contributed equally to this work.
Find articles by Ryals, M. in: JCI | PubMed | Google Scholar
National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Rockville, Maryland, USA.
Address correspondence to: Lisa L. Cunningham, National Institute on Deafness and Other Communication Disorders, NIH, 5 Research Ct., Rockville, Maryland 20850, USA. Phone: 301.443.2766; Fax: 301.402.7580; E-mail: Lisa.cunningham@nih.gov.
Authorship note: Soumen Roy and Matthew M. Ryals are co–senior authors and contributed equally to this work.
Find articles by Van den Bruele, A. in: JCI | PubMed | Google Scholar
National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Rockville, Maryland, USA.
Address correspondence to: Lisa L. Cunningham, National Institute on Deafness and Other Communication Disorders, NIH, 5 Research Ct., Rockville, Maryland 20850, USA. Phone: 301.443.2766; Fax: 301.402.7580; E-mail: Lisa.cunningham@nih.gov.
Authorship note: Soumen Roy and Matthew M. Ryals are co–senior authors and contributed equally to this work.
Find articles by Fitzgerald, T. in: JCI | PubMed | Google Scholar
National Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Rockville, Maryland, USA.
Address correspondence to: Lisa L. Cunningham, National Institute on Deafness and Other Communication Disorders, NIH, 5 Research Ct., Rockville, Maryland 20850, USA. Phone: 301.443.2766; Fax: 301.402.7580; E-mail: Lisa.cunningham@nih.gov.
Authorship note: Soumen Roy and Matthew M. Ryals are co–senior authors and contributed equally to this work.
Find articles by Cunningham, L. in: JCI | PubMed | Google Scholar
Published October 15, 2013 - More info
J Clin Invest. 2013;123(11):4945–4949. https://doi.org/10.1172/JCI71353.
© 2013 The American Society for Clinical Investigation
Received: May 31, 2013; Accepted: August 12, 2013
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Results and Discussion
We developed a sound exposure paradigm that induces HSPs in the mouse cochlea without causing permanent hearing loss. Our goal was to optimize the sound such that it causes a temporary threshold shift (TTS), an indicator that the cochlea is stressed by the sound, but does not produce a permanent threshold shift (PTS). Mice were exposed to an octave band (8–16 kHz) of sound at 90.1 ± 2.7 dB sound pressure level (SPL) for 2 hours. Hearing sensitivity was tested by auditory brainstem response (ABR) measurements before sound exposure and again 24 hours and 1 week later. Twenty-four hours after sound exposure, mice had mean threshold shifts (hearing loss) of 9 to 22 dB (Figure 1A). One week later, hearing sensitivity had recovered to preexposure levels at all frequencies (Figure 1A).
Figure 1Sound preconditioning induces HSPs without causing permanent hearing loss. Mice were exposed to sound preconditioning (8–16 kHz octave band of noise at 90 dB SPL) for 2 hours. (A) Hearing thresholds were measured by ABR. Twenty-four hours after sound exposure, mice had mean TTSs of 9 to 22 dB. Hearing sensitivity returned to pretest levels by 1 week after sound exposure. Asterisks indicate significance between the pretest and 24-hour post-test ABR thresholds (ANOVA, *P < 0.05). (B) Sound exposure did not cause any change in the amplitude of ABR wave I. (C) Cochleas from sound-treated and control mice were collected at 2, 4, 8, and 12 hours after sound exposure. Sound caused the induction of Hsp32 and Hsp70 mRNA in cochleas of sound-treated mice relative to those of untreated (control) mice. Asterisks indicate a significant increase in Hsp mRNA relative to control. (D) Hsp70 induction in response to sound was restricted to the cochlea. Tissues were collected from control and sound-exposed mice 8 hours after sound exposure. Sound exposure induced Hsp70 mRNA in cochlea but not in brain, heart, or kidney. Asterisk indicates a significant increase in Hsp70 mRNA relative to control. Data shown are the means ± SEM.
Sound exposure that does not result in PTS may still cause damage to the inner ear, including loss of afferent nerve terminals (7). This subtle damage is reflected in the ABR as a reduction in the amplitude of ABR wave I (7). We measured wave I amplitudes in mice that had undergone sound exposure 5 times over 12 days (see Methods). Wave I amplitudes were measured prior to the first sound exposure and again 3 weeks after the final sound exposure. There was no change in wave I amplitude between the pretest and post-test ABRs at any frequency (Figure 1B), suggesting that sound exposure resulted in no detectable damage to the auditory system.
We next examined the induction of Hsp mRNA in response to sound exposure. Preconditioning sound induced both Hsp32 (also called heme oxygenase 1, HMOX1, or HO-1) and Hsp70 mRNA expression (Figure 1C). Sound-induced Hsp70 mRNA induction was restricted to the cochlea and was not observed in other organs in sound-exposed mice (Figure 1D).
Studies of cisplatin ototoxicity have been hindered by the lack of suitable mouse models of cisplatin-induced hearing loss (8). Previous models relied on a single injection of high-dose cisplatin, resulting in high toxicity and little reduction in hearing sensitivity (8–10). We developed a new mouse model of cisplatin ototoxicity that approximates the pattern of multiple cycles of cisplatin administration in humans (11–13). We evaluated two cisplatin administration protocols. In the “4×4 protocol,” mice received cisplatin (4 mg/kg) each day for 4 days. The 4-day cisplatin administration period was followed by 10 days of recovery. This protocol was repeated two additional times for a total of three cycles of cisplatin administration (4 days) followed by recovery (10 days). The “8×2 protocol” was similar except that the mice received 8 mg/kg of cisplatin each day for 2 days per cycle for the same cumulative cisplatin dose. Mice underwent hearing testing prior to the onset of cisplatin administration and again 15 days after the final cisplatin injection. Each protocol caused significant hearing loss (Figure 2A). Cisplatin also caused a severe reduction in distortion-product otoacoustic emissions (DPOAEs), a measure of outer hair cell function (Figure 2B). Since the 4×4 protocol caused significantly less weight loss than the 8×2 protocol (data not shown), this protocol was selected for subsequent experiments.
Figure 2Sound preconditioning protects against cisplatin ototoxicity. (A) Mouse model of cisplatin ototoxicity. Mice underwent three cycles of cisplatin administration consisting of 4 mg/kg/day for 4 days (4×4 protocol) or 8 mg/kg/day for 2 days (8×2 protocol) followed by 10 days of recovery. Hearing was tested by ABR before cisplatin administration and 15 days after the final cycle. Cisplatin caused significant permanent threshold shifts across frequencies (ANOVA, *P < 0.05, asterisks indicate significance relative to saline-treated mice. Shown are the means ± SD). (B) Outer hair cell (OHCs) function was examined using DPOAEs. Cisplatin reduced DPOAE amplitudes (ANOVA, *P < 0.05, asterisk denotes significance relative to the saline-treated mice. Shown are the means ± SD). (C) Timeline of cisplatin administration and sound exposures. (D) Mice that received cisplatin alone had significant hearing loss at all frequencies relative to mice that received sound alone or saline alone. Sound preconditioning significantly inhibited cisplatin-induced hearing loss (ANOVA, *P < 0.05, asterisk indicates significance between cisplatin and cisplatin plus sound). (E and F) Cisplatin caused significant loss of OHCs in the upper middle cochlear turn (1.5 mm from the apex) and near-total loss of OHCs in the middle and basal cochlear turns (2.0–3.2 mm from the apex). Sound preconditioning significantly improved OHC survival in the middle and the upper basal turns (ANOVA, *P < 0.05). Scale bar: 20 μm. IHCs, inner hair cells.
To determine whether sound protects against cisplatin-induced hearing loss, mice were treated with the 4×4 cisplatin protocol with or without sound preconditioning. The cisplatin administration and sound exposure procedures are schematized in Figure 2C. Mice that received sound in addition to cisplatin were exposed to sound on days 1, 3, 10, 14, 16, 23, and 28. Mice that received cisplatin without preconditioning sound had moderately severe threshold shifts across frequencies (Figure 2D). Preconditioning sound resulted in significant protection against cisplatin-induced hearing loss (Figure 2D). The protective effect was greatest at 16 kHz, a frequency that was included in the octave sound band, suggesting that the protective effect of sound may be mediated by local effects within the tonotopic (place-frequency) organization of the cochlea.
We analyzed the effect of sound exposure on cisplatin-induced hair cell death. Cisplatin caused extensive loss of outer hair cells in the middle and basal turns (Figure 2, E and F), regions that correspond to the mid- to high-frequency threshold shifts observed by ABR (Figure 2D). Sound inhibited outer hair cell loss in the middle turn, but not in the basal turn (Figure 2, E and F). Together, these data indicate that sound preconditioning protects against hearing loss and outer hair cell death caused by cisplatin.
We next examined whether sound protects against hearing loss caused by the other major class of ototoxic drugs, the aminoglycoside antibiotics. Mice were treated with kanamycin (750 mg/kg s.c.) twice daily for 17 days and then allowed to recover for an additional 3 weeks (2, 4, 14). During the kanamycin administration period, mice were treated with sound every 2.5 days (Figure 3A). Kanamycin caused moderate-to-severe hearing loss (Figure 3B). Sound exposure resulted in partial protection against kanamycin-induced hearing loss (Figure 3B). Sound also inhibited kanamycin-induced hair cell death (Figure 3C). These data indicate that sound provided modest but significant protection against kanamycin ototoxicity.
Figure 3Sound preconditioning protects against aminoglycoside-induced hearing loss and cochlear hair cell death. (A) Schematic diagram illustrating the timeline of kanamycin administration and sound exposures. (B) Mice that received kanamycin had mean PTSs of 10 to 51 dB. Sound preconditioning reduced kanamycin-induced hearing loss, an effect that was significant at 32 kHz (ANOVA, *P < 0.05). (C) Hair cell counts show that sound preconditioning protected hair cells against kanamycin-induced death in the mid-base (3.2 mm from the apex) portion of the cochlea (ANOVA, *P < 0.05).
Our data indicate that sound preconditioning inhibits hearing loss caused by both major classes of ototoxic drugs, and they suggest that sound therapy holds promise as a strategy for protecting the hearing of patients receiving these drugs. Sound therapy has advantages over other potential protective therapies. First, sound therapy is noninvasive. Second, unlike therapies that use systemic administration of otoprotective drugs, the effects of sound therapy are likely to be restricted to the ear. A major requirement of any therapy aimed at inhibiting ototoxic drug–induced hearing loss is that the proposed therapy must not alter the therapeutic efficacy of the primary drug (i.e., the antineoplastic activity of cisplatin or the antimicrobial activity of the aminoglycosides). Some proposed therapies use systemic antioxidants to protect the inner ear. However, the use of supplemental antioxidants in patients undergoing cancer treatment is controversial (15, 16). Because the effects of sound therapy are likely to be restricted to the ear, it is less likely to inhibit the therapeutic efficacy of cisplatin.
Preconditioning sound is also protective against both noise trauma and age-related hearing loss (17–19). The protective effect of conditioning sound is a robust response that has been demonstrated in several species (17, 19, 20), including humans (21). Previous studies have suggested roles for both glucocorticoid receptors (22, 23) and HSPs (19, 24) as mediators of the protective effect of sound conditioning. Adrenalectomy abolishes the protective effect of sound conditioning, and treatment with corticosterone partially restores protection (22, 23). Sound conditioning maintains the activity and nuclear localization of the glucocorticoid receptor (22). HSPs play major roles in the glucocorticoid response by regulating the maturation, nuclear localization, and degradation of the glucocorticoid receptor (25). Thus, sound preconditioning may induce a generalized stress response in which a cohort of protective molecules are induced, possibly including glucocorticoids (22), HSPs (19, 24), and/or antioxidants (26).
While the current study does not directly address the mechanism(s) underlying the protective effect of sound therapy, our previous data on the protective effects of HSPs created a framework for the rational design of the sound exposure paradigm. Sound resulted in the induction of Hsp32 and Hsp70, each of which is protective against ototoxicity in mice (2–5). The mouse genome contains three cytoplasmic inducible Hsp70 genes, two of which are ubiquitously expressed (Hspa1a and Hspa1b). These two Hsp70 genes are 99% identical, and their functions appear to be redundant (27). Since our previous data show that HSP32 is also protective (4), a direct test of whether HSPs are required for the protective effect of sound conditioning will require triple-knockout mice (Hspa1a, Hspa1b, and Hmox1). Since these same HSPs are also important safeguards against nephrotoxicity caused by aminoglycosides and cisplatin (28, 29), a conditional (ear-specific) triple knockout will be necessary to determine whether HSPs are required for sound-induced protection.
Our data indicate that sound preconditioning inhibits hearing loss caused by both major classes of ototoxic drugs. Given the potential advantages of sound therapy, these data suggest that sound preconditioning holds potential to protect the hearing of patients receiving these drugs.
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