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. 2016 May 7;20:1389–1401. doi: 10.1007/s00784-016-1828-x

Table 1.

Overview of studies involving animal models investigating the role of the tensor veli palatine muscle in Eustachian tube opening

Authors Year Aim(s) of the study Subjects Characteristics age/weight (range) Results Conclusion(s)
Honjo et al. [22] 1979 Identify muscle responsible for tubal opening using EMG and electrical muscle stimulation. 12 dogs NR/NR Stimulation of TVP resulted in drop of pressure in middle ear space, whereas LVP stimulation did not affect pressure. (1) TVP is the only active tubal dilator in dogs
(2) LVP has no effect in ET dilation
Cantekin et al. [23] 1979 Verify results of previous studies showing the TVP as only tubal dilator. 5 juvenile macaque monkeys NR/2.5–4 kg (1) Stimulation of mandibular nerve produced a pressure-flow drop in ET similar as recorded during swallowinga.
(2) Pressure-flow drops were no longer observed following TVP transection.
(1) TVP is the only active tubal dilator in rhesus monkeys.
(2) Mandibular nerve innervates the TVP
Honjo et al. [24] 1980 Examining (1) synergistic action between TVP and LVP and (2) ET opening process using contrast fluid and cineradiographic analysis while stimulating the muscles. 4 macaque monkeys NR/4–10.5 kg (1) TVP stimulation resulted in drop of tympanal pressure, while LVP stimulation did not affect pressure.
(2) LVP stimulation caused inward movement of the torus tubarius and thus widening of the pharyngeal orifice. TVP stimulation opened the proximal part of the ET through outward displacement of the lateral tubal wall.
(1) TVP is the sole ET opener.
(2) LVP dilates the ET only at its pharyngeal orifice, while the TVP opens the ET by pulling the lateral wall outwards.
Cantekinet al. [25] 1980 Examining the effects of surgical TVP procedures (excision, transection, transposition) on ET function and ME status. 22 juvenile and adult macaque monkeys NR/2–6 kg (1) TVP excision caused chronic OME and complete tubal dysfunction.
(2) TVP transection lead to abnormal ME pressure, effusion, or both with a transient, recurrent or chronic character. The ET was initially dysfunctional, however slowly regained function. (3) TVP transposition had initially similar effects as transection, though ME pathology and ET function improved more rapidly.
Surgical manipulations of the TVP created a functional ET obstruction; the severity of ET dysfunction depended on the performed surgical procedure with excision being the most harmful.
Casselbrant et al. [26] 1988 Investigate the effects of TVP paralysis (using botulinum toxin Ab) on ET function and ME status. 8 adult macaque monkeys NR/5–9 kg 10/12 examined ears develop flat tympanograms within 8–30 days indicating middle ear effusion (confirmed in 7 ears by tympanoscentesis). Tympanograms required 13–32 days to normalize. Injecting botulinum toxin A into the TVP creates reversible functional ET obstruction which became evident as high-negative pressure followed by middle ear effusion.
Ghadiali et al. [27] 2003 Investigate the effects of TVP paralysis (using botulinum toxin Ab) on ET tissue dynamics. 12 macaque monkeys NR/2–4 kg Loss of TVP muscle tone and stiffness resulted in significant decrease of ET opening pressure, increased ET compliance and reduced ET viscoelasticity. Paralysis of TVP by botulinum toxin results in decreased function due to alterations of ET mechanical properties.

ET Eustachian tube, EMG electromyography, TVP tensor veli palatini muscle, LVP levator veli palatini muscle, ME middle ear, OME otitis media with effusion, NR not reported

aSwallowing was induced by pharyngeal stimulation

bBotulinum toxin A is known for its paralyzing effects by working on acetylcholine release at the neuromuscular junctions