Sensory response following knee joint damage in rabbits

Sensory information from mechanoreceptors in peri-articular tissues play a crucial role in proprioception, motor control and dynamic joint stability [1]. Altered sensory information arising from damaged knee joint structures has been hypothesized as a contributing factor to persistent dysfunction following injury such as altered proprioception, force production and coordination [2, 3]. In the knee joint, afferent information arises from nerves that innervate muscles crossing that joint. Innervation to the knee joint capsule has been characterized in animal and human anatomic experiments and includes projections from the obturator, saphenous and femoral nerves [4]. Therefore, sensory information from pain, pressure and stretch receptors such as free nerve endings, pacinian corpuscles and ruffini endings would be conveyed along these nerve projections resulting in a composite afferent signal conveyed to the central nervous system. The sensory effects of knee joint injury have been reported in humans indirectly as the underlying cause of arthrogenic muscle inhibition (AMI) [3, 5]. In theory, altered sensory information arising from mechanoreceptors within damaged knee joint structures results in an ongoing reflexive response causing a reduction in spinal reflex excitability [6]. Therefore, characterization of a composite afferent signal following knee joint injury or surgery would help develop a better understanding the sensory response to joint injury and possibly explain potential underlying causes of AMI.

Recent investigations have shown the femoral nerve composite sensory signal changes following MCL disruption in rats [7, 8]. However, Rabbits have also been used in models of knee injury, muscle weakness and osteoarthritis. The large mammalian nervous system and knee joint anatomy of rabbits provide an adequate model for studying the effects of intra-articular knee ligament injury or reconstructive surgery. Rabbit models of knee injury, osteoarthritis and muscle dysfunction have been described [2, 9–14]. For example, quadriceps muscle weakness [11] and atrophy [10] were observed in rabbits with transected anterior cruciate ligaments (ACL) suggesting the role of posttraumatic quadriceps dysfunction in the onset and progression of osteoarthritis. Further, muscle weakness induced by botox injections caused increased cartilage degeneration in rabbits [13]. However, a model to study composite afferent signals arising from the femoral nerve in the presence of ACL injury or reconstruction has not been developed.

Therefore the purpose of this study was to compare femoral nerve afferent signal using a whole nerve recording technique in rabbits 2-weeks following knee joint trauma. We hypothesized that the damage caused by injury and surgery would cause an increase in afferent activity from sensory endings located in tissues within and surrounding the knee joint thereby increasing composite signal measured from the femoral nerve in rabbits with knee joint injury and reconstruction surgery compared to controls due to increase afferent activity from sensory endings.

This study was reviewed and approved by the Institutional Animal Care and Use Committee at the University of Virginia. Twenty-four adult, male New Zealand White rabbits were randomized into one of 3 intervention groups. Eight of the rabbits received unilateral ACL transection, 8 of the rabbits received an ACL reconstruction and the remaining 8 were control rabbits who received no intervention. The side receiving the surgical intervention was randomly allocated.

The primary finding in this study is that composite sensory information measured on the femoral nerve was higher in animals with knee joint injury compared to controls. The differences in side-side ratios were only present in animals in the ACL-R group. The surgical groups were intended to model a scenario of ACL injury with instability versus ACL injury with stability restored through autograft patellar tendon reconstruction. The findings of higher side-side ratios in the ACL-R group suggest that the additional damage created in the knee joint due to the reconstruction procedures resulted in changed sensory information detected in the femoral nerve. Reconstructed knees underwent partial removal of the patellar tendon, potential damage to the joint structures due to tunnel drilling, graft passage and fixation and a more extensive arthrotomy and longer surgical time compared to the ACL transection group. Therefore, these findings suggest that the extent of damage caused by the surgical intervention may explain the observed group differences.

In clinical research, poorer outcomes have been reported in patients with more severe knee joint injuries. For example, higher magnitude quadriceps arthrogenic muscle inhibition has been reported in patients with more severe or extensive joint structure damage [6, 16, 17]. In addition, patients with recurrent knee injuries such as a failed graft following ACL reconstruction surgery have exhibited poorer self-reported outcomes [18]. Finally, greater impairments in knee joint proprioception was reported in patients with ACL deficient knees reporting instability [19]. Therefore, it is possible that the side-side differences in nerve signal observed in the ACL reconstruction group was due to the addition knee joint damage due to the reconstruction procedures.

In the current study, we observed higher magnitude composite afferent signal in knees that underwent ACL reconstruction compared to control animals. The signal measured from the femoral nerve may include several sources of afferent information. For example, articular structures within and around the knee joint contain nerve receptors such as free nerve endings, pacinian corpuscles and ruffini endings [20, 21]. These receptors are innervated by articular branches from the femoral, saphenous, obturator, tibial, common peroneal, and recurrent peroneal nerves [22]. In feline models, it has been reported that the anterior and posterior knee joint capsule is densely innervated with Ruffini endings [23] which are slowly adapting mechanorecptors that respond to capsular stretching [24]. The innervation of the knee joint is dispersed among the various nerve branches. Knee joint innervation has been previously divided into anterior (articular branches from the femoral, common peroneal and saphenous nerve) and posterior (articular branches from the tibial and obturator nerves) [4]. The exact articular distribution is unknown in rabbits, but in other mammalian systems, components of the anterior group of nerve fibers, including the femoral and saphenous nerve articular branches, terminate on structures around the anterior, medial and lateral aspects of the joint capsule and anterior cruciate ligament [4]. Posterior group afferents terminate on posterior structures and the posterior cruciate ligament. Interestingly, branches from the saphenous nerve and the obturator nerve have been reported to form a nerve plexus innervating the posterior capsular structures. In the current study, we certainly did not capture all of the sensory information because we did not record from obturator, tibial or common peroneal nerves. The composite information recorded in the current study likely included information from the femoral nerve and its sensory branch, the saphenous nerve. Therefore femoral nerve signal measured in the current study is most likely attributed to afferent signal arising from articular structures innervated by the femoral and saphenous nerves.

In the current study, we observed higher magnitude composite signal from the femoral nerve in the reconstructed group only. This finding highlights the fact that the anterior cruciate ligament may play an important role in conveying sensory information [4]. Mechanoreceptors such as pacinian corpuscles, golgi tendon organs, and ruffini endings are heavily clustered at the proximal and distal poles of the anterior cruciate ligament [22, 25–27] giving rise to afferent proprioceptive information. During an ACL reconstruction, it is likely that terminal branches of sensory nerves are severed as a natural consequence of the surgical procedure so its not clear what sources play a role in conveying sensory information following ACL injury and reconstruction. In the post-amputee literature ectopic afferent, nociceptive signaling has been hypothesized to arise from nerve sprouting from severed nerves [28]. In the current study there may be potential relationship between the loss of tissue and afferent input. For example, reconstruction techniques where the ACL remnants are preserved [29–31] have been described as having good outcomes [32]; attributed to improved improved vascularization and re-innervation due to the ACL remnant [33, 34]. The presence of a remnant in the ACL-T group is one differentiating factor that may partially explain why this group did not have increased composite afferent signal. The role of tissue preservation and sensory input is an area for future research.

Joint damage often leads to arthrogenic muscle inhibition in the quadriceps musculature [35]. Arthrogenic muscle inhibition is a unique phenomenon because it exists despite no injury or pathology to the efferent nerve or target muscle. In theory, arthrogenic muscle inhibition is a reflexive response to aberrant sensory information arising from damaged joint structures resulting in a failure to voluntarily activate motor units. The response of Ruffini endings to capsular stretching due to laxity or joint effusion has been implicated in reflexive muscular inhibition that is commonly seen in patients with extensive knee injuries [3, 5]. In humans, this manifests as persistent muscle weakness, altered gait patterns and joint degeneration [36]. While this may be a protective response in the acutely injured knee, the long term outcome in persistently inhibited musculature can result in dysfunction. Therefore, if arthrogenic muscle inhibition is persistent following joint injury, recovery may be impeded. In clinical populations, the quadriceps [16] muscle is commonly affected by arthrogenic muscle inhibition which often leads to impaired movement during walking gait [37]. Increased afferent information is currently hypothesized to contribute to post-traumatic muscle inhibition. The findings from the current study may be the basis of future investigations into the potential relationships among increased afferent information and quadriceps muscle dysfunction and osteoarthritis in the post-traumatic knee.

There are some limitations to the study due to the possiblity that other factors associated with knee joint injury, such as inflammation and associated chemical mediators, sensitize afferent nociceptive neurons, which may also contribute to altered sensory information in the post-traumatic knee [38]. However, we feel that the potential influence of chronic inflammation was minimal because upon examining the medical records, none of the rabbits were showing any outward signs of inflammation at the time of follow up evaluations nor any changes in behavior that would indicate the animals were in pain. All were active and healthy at the time of terminal measurements therefore our conclusions are made based on measurements recorded when rabbits were in good health and recovered from their knee joint surgery. Another limitation is the lack of comparison to baseline measurement. Unfortunately, due to the terminal nature of the measurement technique, baseline measurements were not able to be recorded prior to surgery.

We observed higher side-to-side ratios of peak, composite afferent signal measured directly from the femoral nerve during passive knee extension in rabbits, 2 weeks following ACL reconstruction. This difference suggests higher magnitude sensory information from damaged knee joint structures. This increase in sensory afference may play a role in reflex quadriceps muscle inhibition that is commonly observed in the post traumatic knee.