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Monoaminergic mediation of masculine and feminine copulatory behavior in female rats.

Ovariectomized rats treated with testosterone propionate (TP; 100 mug/kg X 6 days) and para-chlorophenylalanine (pCPA; 100 mg/kg X 3 days), a serotonin synthesis inhibitor, showed more masculine copulatory behavior (including the ejaculatory pattern) than did females receiving either TP or pCPA alone. The facilitatory effect of pCPA on the masculine copulatory behavior in females was not potentiated by pargyline (50 or 100 mg/kg), a monoamine oxidase inhibitor; instead, pargyline antagonized the effect of pCPA. Apomorphine (100 mug/kg), a dopamine receptor stimulant, did not increase masculine copulatory behavior in TP treated females. Adopaminergic facilitatory effect was therefore not demonstrated. These results suggest a serotonin-mediated inhibition of masculine copulatory behavior in female rats. When feminine copulatory behavior was tested, females receiving TP plus pCPA plus pargyline, TP plus pargyline, or TP plus apomorphine displayed lordosis in response to mounting by male rats. Lordosis did not occur after administration of TP, PCPA, or pargyline, individually or in any other combination. The responses in pargyline groups are consistent with the hypothesis of a noradrenergic facilitatory system for lordotic behavior. The responses in the apomorphine group are discussed in terms of a possible role for low level dopaminergic stimulation in facilitating lordosis.

Adrenal Glands↗

Delta-9-Tetrahydrocannabinol stimulates receptive and proceptive sexual behaviors in female hamsters.

This experiment studied the effects of delta-9-tetrahydrocannabinol (THC) on lordosis responses and ultrasonic communication (measures of sexual receptivity and proceptivity, respectively) in female hamsters. Specifically, lordosis durations and rates of ultrasound production by estradiol-primed ovariectomized hamsters were observed following acute treatment with 1.5 mg/kg of THC, 500 micrograms of progesterone, or the injection vehicle. The results showed that THC can facilitate both lordosis and ultrasound production. Together with results from other laboratories, these data indicate that THC can stimulate female sexual behavior and suggest that this effect reflects a direct, nonhormonal, effect of THC on brain mechanisms for behavior.

Animals↗

Influence of estrogen and progesterone on behavioral effects of apomorphine and amphetamine.

A study was made of the influence of apomorphine. D- and L-amphetamine on the effects of different hormonal treatments used to induce copulatory behavior in female rats. Female copulatory behavior, (lordosis response), which has been shown to be inhibited by increased DA and 5-HT neuronal activity, was depressed by apomorphine, D- and L-amphetamine in ovariectomized rats treated with estrogen + progesterone. When lordosis behavior was activated by estrogen alone the inhibitory action of the drugs, especially that of apomorphine was considerably less pronounced. However, the effect of D-amphetamine on stereotype activity was not greater after treatment with estrogen + progesterone than after administration of estrogen alone. Estrogen had a slight stimulatory effect on stereotype activity in non-drug-treated rats, while progesterone had an inhibitory effect. Possible mechanisms underlying the observed interactive effect of progesterone and monoamines on lordosis behavior, such as a progesterone-induced alteration of monoaminergic transmission, are discussed.

Amphetamine↗

The role of endogenous opioids in the blockade of reproductive function in the rat following exposure to acute stress.

The present experiments investigated the involvement of endogenous opioids in the preovulatory disruption of luteinizing hormone release and ovulation following exposure to an acute stressor. The effect of exposure to an acute stressor and/or treatment with naloxone hydrochloride on the proestrus/estrus display of lordosis behavior is also reported. Electric shocks (2 mA) delivered at 10-min intervals for three hours during the period of the preovulatory luteinizing hormone surge in adult cyclic female rats resulted in the blockage of luteinizing hormone release, decreased lordosis behavior, and inhibition of ovulation. The anti-luteinizing hormone and anti-ovulatory actions were antagonized by the administration of naloxone hydrochloride shortly prior to the application of the stressor, which suggests that the observed blockage of ovulation is mediated by endogenous opioids known to be elevated in response to a stressor. It is argued that the most likely mechanism by which endogenous opioids inhibit luteinizing hormone release and ovulation is by inhibiting luteinizing hormone releasing hormone release, and/or decreasing its production in the hypothalamus. In contrast, naloxone only partially antagonizes the anti-lordotic actions of electric shock. It is therefore further argued that the inhibition of luteinizing hormone release alone is not sufficient to explain the dramatic decrease in lordosis behavior observed following exposure to an acute stressor. Adrenal progesterone released in response to adrenocorticotropic hormone release following exposure to an acute stressor, in association with inhibited luteinizing hormone releasing hormone release is hypothesized to be responsible for the observed decrease in lordotic behavior, and the inhibition of luteinizing hormone release.

Animals↗

Administration of gonadotropin-releasing hormone to pregnant rats inhibits postpartum sexual behavior.

Administration of gonadotropin-releasing hormone (GnRH) can both facilitate sexual behavior in estrogen-primed, ovariectomized rats and induce numerous antifertility effects in pregnant rats. The present study was undertaken to determine the effect of GnRH treatment on 1) sexual behavior of rats during late pregnancy and at postpartum and 2) plasma levels of dihydrotestosterone (DHT) and progesterone (P), two hormones implicated in the regulation of sexual behavior during pregnancy. Rats were given either 4 micrograms or 12 micrograms GnRH or no treatment on day 18 of pregnancy. On days 18 (4 hr posttreatment) and 19 of pregnancy, the day of parturition and the day following parturition, each rat was tested for lordosis response to male mounts and subsequently bled from the jugular vein for determination of plasma DHT and P levels by radioimmunoassay. Both doses of GnRH significantly inhibited lordosis at postpartum estrus and failed to induce lordosis on days 18 and 19 of pregnancy and the day following parturition. DHT was suppressed on day 19 and at postpartum; P was elevated on the day following parturition. Our data demonstrate that as little as 4 micrograms GnRH can induce postpartum "behavioral antifertility" effects without apparent detriment to the pregnancy.

Animals↗

Development of steroid-receptor systems in guinea pig brain. I. Cytoplasmic estrogen receptors.

The development of the cytoplasmic estrogen receptor (CER) system in male and female guinea pigs was examined to determine whether attainment of sensitivity to estrogen action related to lordosis behavior is correlated with increases in brain CER concentrations. Ovariectomized neonatal (7 days old) guinea pigs failed to display lordosis after priming with 10 micrograms estradiol benzoate (EB) and 0.5 mg progesterone (P). The percentage of ovariectomized steroid-treated females displaying lordosis increased at 29-33 days of age. At 50-65 days of age this percentage increased even further. Plasma levels of estrogen in 4-6 day old animals at 4, 8 and 12 h after 10 micrograms EB were at least equal to those seen in 50-65 day old animals. Neither the concentration nor the affinity of CER in hypothalamus (HYPO), preoptic area (POA), amygdala (AMYG) and cortex ( CORT ) were different in 4-6 day olds vs 50-65 day olds. The rank order for concentrations of CER in brain regions was: POA greater than HYPO greater than AMYG greater than CORT . A sex difference in CER was found in HYPO (females greater than males), but not POA, AMYG or CORT of 4-6 day olds.

Animals↗

Gamma aminobutyric acid mediates ventromedial hypothalamic mechanisms controlling the execution of lordotic responses in the female rat.

To study the participation of gamma-aminobutyric acid (GABA) in the control of sexual behavior in the female rat, the effect of GABA and picrotoxin injections in the ventromedial hypothalamic nucleus (VMN) upon lordosis frequency and multiunit spike activity (MUSA) was determined. Infusion of 100 micrograms GABA into conscious rats reduced lordotic responsiveness within 15 min after injection; with a similar time course, the same dose markedly reduced MUSA in urethane anesthetized rats. Forty-five min after injection lordotic responsiveness recuperated to preinjection levels; at this time MUSA showed a rebound increase in neuron firing frequency. The possible relation between ventromedial hypothalamic neuronal activity and capacity for lordotic responses was further tested with injections of a local anesthetic: 1 microliter of 2% Xylocaine infused into the VMN produced similar results, suppressing MUSA and lordotic responsiveness for ca. 45 min beginning immediately after injection. Microinjections of GABA antagonist picrotoxin had the opposite effects: 0.1 microgram increased MUSA and lordotic responsiveness at 5 and 45 min; however at 20 min, when MUSA was at its highest, lordosis frequency was not elevated. Injections of solvent had no consistent effects on either measure. Two conclusions many be tentatively drawn from these data: (a) the VMN is the origin of a neural signal which exerts a moment-to-moment gating control on the execution of lordosis, and (b) the generation and/or the output of this signal is under the control of a GABAergic hypothalamic mechanism which normally exerts an inhibitory effect on the display of lordotic responses.

Action Potentials↗

Effects of nucleus accumbens lesion on female rat sexual receptivity and proceptivity in a partner preference paradigm.

A partner preference paradigm, stud male vs estrous female, was used to study sexual behavior. Ovariectomized Wistar rats received bilateral electrolytic (n = 33) or sham (n = 16) lesion of the nucleus accumbens. Animals were tested in two different experimental situations, either with stimulus animals tethered (test with possibility of mating) or with stimulus animals behind a wire mesh (test without possibility of mating). Each test was carried out once prior to surgery and twice postoperatively following priming with estradiol benzoate and progesterone. Lordosis, rejection behaviors and soliciting patterns were scored in tests with tethered stimulus animals. The tendency of the experimental female to approach and remain in the vicinity of each stimulus animal was quantified to study the partner preference. Nucleus accumbens lesion increased the number of rejection responses to male mount attempts without modifying either receptivity estimated by lordosis reflex or soliciting behaviors. Control females showed a statistically significant preference for the male throughout the experiments. Lesioned females exhibit a preference for the male only in the test without sexual interaction possibility. This preference disappeared in the test with possibility of mating and it was even reversed when the male showed copulatory activity. These results, together with the absence of changes in lordosis behavior and soliciting activity, suggest that both the inversion in preference and the higher levels of mount rejections found in the lesioned animals are more likely attributable to hyperreactivity to the copulatory stimulus rather than an alteration in the female's rat sexual motivation.

Animals↗

A microdialysis study of ventral striatal dopamine during sexual behavior in female Syrian hamsters.

Microdialysis was used to study the effects of exposure to a male hamster on extracellular concentrations of dopamine, dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), and 5-hydroxyindole acetic acid (5-HIAA) in the ventral striatum of ovariectomized female Syrian hamsters pretreated with either estradiol and progesterone, or a similar regimen of oil injections. The hormone-treated females showed high levels of lordosis throughout the hour of exposure to the male. In hormone-treated females, there was a rapid elevation of dialysate dopamine within the first 15 min of exposure to the male. Dialysate dopamine gradually declined over the next 45 min, though remaining significantly above baseline during the entire period of exposure to the male. None of the oil-treated females showed any indication of lordosis, and the addition of the male produced only a small increase in dopamine at 30 min, after which dopamine returned to pre-male basal levels. DOPAC, HVA, and 5-HIAA were all elevated following introduction of the male for both groups of females. These results suggest that ovarian hormones modulate the responsivity of ventral striatal dopamine to incentive stimuli associated with mating behavior in females, although extracellular levels of dopamine in the ventral striatum do not seem to be directly coupled to the display of lordosis.

3,4-Dihydroxyphenylacetic Acid↗

Behavioral effects of 3 alpha-androstanediol. II: Hypothalamic and preoptic area actions via a GABAergic mechanism.

We investigated whether 5 alpha-androstane-3 alpha, 17 beta-diol (3 alpha-androstanediol; 3 alpha-Diol), a neurosteroid whose effects are primarily inhibitory to sexual behavior, may act through interactions with gamma-aminobutyric acid (GABA) receptor complexes (GBRs) in the medial basal hypothalamus (MBH) and the preoptic area (POA). In Experiment (Exp.) 1, ovariectomized (ovx) rats were implanted with bilateral guide cannulae aimed above the MBH and were later treated with 17 beta-estradiol (E2, 2 injections of 1 microgram/0.2 ml in 10% ethanol) and either 3 alpha-Diol (3.0 mg/kg, s.c.) or vehicle. Progesterone (0.5 mg, s.c.) was given 24 h after the first E2 injection and a pre-test for lordosis responsiveness was carried out 4 h later. The GABAA agonist, muscimol (50 ng), then was infused into the MBH and rats were tested 10, 30 and 60 min later. Muscimol infusion facilitated lordosis behavior in vehicle-treated controls, but 3 alpha-Diol-treated animals failed to show this facilitation. To ascertain whether 3 alpha-Diol would also prevent muscimol's action in the POA, a site in which muscimol inhibits, rather than facilitates, sexual receptivity, ovx animals in Exp.2 were implanted with bilateral guide cannulae aimed above the POA and were treated with E2, 3 alpha-Diol, and P and infused and tested as in Exp. 1. Muscimol and 3 alpha-Diol each significantly inhibited receptivity; when they were combined, the inhibition was more pronounced. In Exp. 3, POA infusions of the GABAA antagonist, bicuculline, counteracted muscimol's and 3 alpha-Diol's inhibition of sexual behavior. In Exp. 4, in vitro treatment of POA and MBH membrane fractions with 3 alpha-Diol (30 microM) enhanced maximal [3H]muscimol binding without altering the affinity of the binding sites for the agonist. These data suggest that 3 alpha-Diol inhibits E2 and progestin-induced lordosis behavior via actions at the GBR in both the MBH and POA.

Androstane-3,17-diol↗

Estradiol induction of proenkephalin messenger RNA in hypothalamus: dose-response and relation to reproductive behavior in the female rat.

Hormone effects on proenkephalin (PE) mRNA allow an opportunity to compare a brain region-specific molecular change with a quantifiable behavior. Slot blots were used to measure PE mRNA levels in the ventromedial hypothalamus (VMN) and preoptic area (POA) as a function of the dose of estrogen administered to ovariectomized rats. Every rat used had been characterized for the ability to display lordosis behavior. Estradiol treatment led to a monotonic dose-dependent increase in PE mRNA level in VMN, while only a small effect was observed in POA at the higher estradiol doses. Lordosis behavior, assessed manually and in mating tests, also increased monotonically with estradiol dose. The data indicate that an apparent 'threshold' level of PE mRNA in VMN coincided wit display of behavior, and suggest further that high levels of PE mRNA, alone, are not sufficient for lordosis. While the exact relationship of the eventual product, Met-enkephalin, to female reproductive behavior remains to be determined, the parallel changes in PE mRNA level and behavior encourage further analysis.

Animals↗

Modifications in gonadotropin control and reproductive behavior in the female rat by hypothalamic and preoptic lesions.

Effects of small hypothalamic and preoptic area lesions on vaginal cyclicity, ovulation and ovarian weights of female rats were examined. Animals were then gonadectomized and tested for lordosis behavior following injections of estrogen alone and estrogen plus progesterone. Male sex behavior was also measured during daily treatment with testosterone. Relative to sham operated rats, lesions in the dorsal preoptic area produced a significant increase in lordosis behavior, virtual elimination of male sex behavior, and only marginal effects on ovarian function. Animals with lesions in the ventral preoptic area showed constant vaginal cornification, lack of ovulation and significantly smaller ovaries than the other groups. These rats also tended to show more female sex behavior and less male sex behavior than sham operated rats. Animals with lesions in the anterior hypothalamus and dorsomedial hypothalamus showed normal ovarian function and levels of female and male sex behavior comparable to the ventral preoptic lesioned rats. Animals with lesions in the ventromedial hypothalamus tended to show lower levels of lordosis behavior than sham animals but displayed a dramatic and significant increase in male copulatory behavior relative to the other groups. These data indicate a clear dissociation between the neural control of cyclic gonadotropin activity and sex specific reproductive behavior.

Animals↗

Female sexual behavior in the golden hamster following kainic acid lesions in the lateral septal area.

Patterns of female sexual behavior in the hamster are qualitatively different from that observed in the rat. Hamsters demonstrate tonic immobility and a sustained lordotic response that can last for several minutes following minimal stimulation from the male while in rats, the lordotic response is highly dependent upon continued stimulation from the male and lasts for only a few seconds following a mount or intromission. Also, the hamster requires both estrogen and progesterone priming in order to display female sexual behavior but the rat can show lordotic behavior following treatment with estrogen alone. Electrolytic lesions in the lateral septal area of female rats produce a facilitation in female sexual behavior and increase behavioral sensitivity to estrogen. However, lesions in the lateral septal area of rats produced by the neurotoxin kainic acid (KA) result in deficits in female sexual behavior following estrogen and progesterone treatment. Given these species differences in sexual behavior, we have examined the effects of KA lesions in the lateral septal area of hamsters on female sexual behavior. Adult female golden hamsters were ovariectomized and tested for female sexual behavior prior to receiving brain surgery. For all behavior tests, animals were injected SC with 60 micrograms of estradiol benzoate/kg per day for two days and 0.5 mg of progesterone three hours prior to the behavior test on day three. Behavior tests consisted of placing the test animal in a male's home cage for 10 minutes and recording the latency to the first lordosis, length of the longest single bout of lordosis and total lordosis duration.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Site-specific inhibition of receptivity by intracranial anisomycin in hamsters.

The ventromedial nucleus of the hypothalamus (VMH) has been implicated in the mediation of the hormonal control of female rodent sexual behavior. However, in hamsters, progesterone (P) has been found to have effects on sexual receptivity in other diencephalic and mesencephalic sites as well. Progesterone is thought to exert its behavioral effects by altering protein synthesis in CNS target neurons. We tested the effects of 30 gauge implants of the protein synthesis inhibitor anisomycin in the preoptic area (POA), VMH, and ventral mesencephalon (VMES) 30 minutes before 500 micrograms P SC, on the facilitation of lordosis in ovariectomized estrogen-primed female hamsters. The same animals were tested one week later with estrogen and progesterone treatment but without anisomycin. Anisomycin reduced sexual receptivity (lordosis) when placed in the VMH or VMES, but not when delivered to the POA. The results confirm the importance of the VMH in the mediation of progesterone facilitation of female sexual behavior, but also provide evidence that ventral midbrain structures may play a role in female sexual receptivity in hamsters. These two structures may be important for different aspects of lordosis. Progesterone effects in both sites appear to be protein synthesis dependent.

Animals↗

The effect of sagittal alignment on adjacent joint mobility after lumbar instrumentation--a biomechanical study of lumbar vertebrae in a porcine model.

BACKGROUND: The mechanisms and changes in range of motion of neighboring mobile segment (adjacent level) after the instrumented posterior stabilization are not completely understood. This study aims to investigate the effect of sagittal alignment on the adjacent joint mobility after lumbar instrumentation. METHODS: Eight fresh porcine lumbar spines were instrumented with pedicle screw implants from L2 to L4. Each specimen was tested in three different sagittal alignments. Group A were instrumented in lordotic alignment (lordosis 20 degrees ), Group B in straight alignment (lordosis 0 degrees ), and Group C in kyphotic alignment (kyphosis 20 degrees ). Hydraulic testing machine was used to generate an increasing moment in flexion and extension respectively for each specimen. The vertebral displacement of the disc between L1-L2 and L4-L5 were measured simultaneously with an extensometer. FINDINGS: There were no significant differences in vertebral displacement between the three different sagittal alignments in both the superior and inferior adjacent segments under extension motion. However, under flexion motion, the vertebral displacement on the superior adjacent segment (L1-L2) with kyphotic alignment was statistically larger than that of the straight and lordotic alignments (P = 0.0198 and P = 0.000473 respectively), and no differences were found between the three different sagittal alignments on the inferior adjacent segment (L4-L5). INTERPRETATION: The iatrogenically produced kyphotic lumbar spine by posterior instrumentation might cause larger adjacent joint mobility on the superior adjacent joint as compared to the instrumented lordotic lumbar spine. This study implies that an instrumented spine in lordosis is less likely to develop adjacent instability than a kyphotic spine.

Animals↗

Management of a chronic lumbar disk herniation with chiropractic biophysics methods after failed chiropractic manipulative intervention.

OBJECTIVE: To discuss the use of chiropractic biophysics methods in the treatment and rehabilitation of a patient with a chronic disk herniation at the L5-S1 disk, retrolisthesis of L5, and a reduced lumbar lordosis. CLINICAL FEATURES: A 23-year-old woman suffered from chronic unremitting symptoms of lower back pain and left-leg pain. She was treated five years prior, without relief. Diagnosis at that time was low-back pain and lumbar subluxation. Approximately 3 years later, she was evaluated by an orthopedic surgeon. Magnetic resonance imaging showed a moderate posterior disk protrusion at L5-S1 with degeneration. INTERVENTION AND OUTCOME: Chiropractic treatment of this patient consisted of mirror-image chiropractic adjustments, 3-point bending lumbar extension traction, and postural exercises. The patient responded well with a complete resolution of her symptoms and a restoration of her lumbar lordosis. CONCLUSION: This article suggests that successful management of chronic low-back pain symptoms may require a close analysis of a patient's postural deviations and sagittal plane curves. This study suggests that it is possible to restore lumbar lordosis in some cases and this may have an unforeseen benefit to the patient. Further study is warranted into the treatment of chronic low-back pain with chiropractic biophysics methods.

Adult↗

Role of glutamate receptors in the ventromedial hypothalamus in the regulation of female rat sexual behaviors. II. Behavioral effects of selective glutamate receptor antagonists AP-5, CNQX, and DNQX.

Bilateral infusions of glutamate or its selective ionotrophic receptor agonists to the ventromedial hypothalamus (VMH) produce a rapid inhibition of both appetitive and consummatory sexual behavior in hormone-primed female rats. The present study examined whether infusion of selective ionotrophic glutamate receptor antagonists to the VMH can facilitate female sexual behavior in females treated with estradiol benzoate (EB) and progesterone (P), or EB alone. Ovariectomized, sexually experienced female rats were implanted bilaterally with guide cannulae aimed at the ventrolateral VMH. After recovery from surgery, females were primed either with EB+P or EB alone, and infused with saline, or one of two doses each of AP-5 (to target NMDA receptors), CNQX, or DNQX (to target AMPA/kainate receptors), immediately before tests with sexually vigorous male rats in bilevel chambers. In general, the drug infusions had a more powerful effect in females primed with EB alone compared to females primed with EB+P. AP-5 increased lordosis in females primed with EB alone. CNQX had a similar facilitative effect on lordosis, and also increased solicitations. DNQX increased solicitations in both hormone-priming conditions, increased lordosis quotients and magnitudes, and decreased pacing and defensive responses in the EB-alone condition. These results indicate that antagonism of glutamate receptors in the VMH resembles the effect of P, and that the addition of P to an EB baseline eliminates most of the effects of glutamate receptor antagonists. These data support the notion that glutamate receptors in the VMH contribute a strong inhibitory influence in the control of female sexual behavior.

2-Amino-5-phosphonovalerate↗

Posterior lumbar interbody fusion for degenerative spondylolisthesis: restoration of sagittal balance using insert-and-rotate interbody spacers.

BACKGROUND CONTEXT: Although satisfactory clinical outcomes have been reported for degenerative spondylolisthesis using a variety of surgical techniques, its optimal management remains controversial. Laboratory and clinical evidence is emerging that if fusion surgery is undertaken, improved short- and longer-term outcomes may be achieved by correcting any sagittal deformity present. The insert-and-rotate posterior lumbar interbody fusion (PLIF) technique, first described by Jaslow in 1946, may enable surgeons to safely and effectively correct sagittal balance through a single posterior approach. PURPOSE: To examine the clinical outcomes and determine whether the focal sagittal imbalance associated with a degenerative lumbar spondylolisthesis can be safely and effectively corrected using a posterior distraction/reduction technique and insert-and-rotate interbody fusion spacers. STUDY DESIGN/SETTING: A prospective, single-cohort, observational study of the clinical outcomes and retrospective radiological review, in a series of 34 patients with degenerative spondylolisthesis, who underwent surgery between September 2000 and October 2002. PATIENT SAMPLE: Mean age of 65.1 years (range, 35 to 82 years). Thirty-two of the 34 patients underwent surgery principally for the relief of radicular leg pain. The principal indication for the fusion was the prevention of anticipated postdecompression instability in 68% of the patients. Mean preoperative slip was 20.0% (range, 12% to 33%). Mean preoperative focal lordosis was 13.2 degrees. OUTCOME MEASURES: Patients were administered pre- and postoperative clinical outcome surveys recording Visual Analogue Pain Score (VAS), Low Back Outcome Score (LBOS), Short Form (SF)-12 and patient satisfaction questionnaires. Pre- and postoperative measurements of the percentage slip and lumbar lordosis of the involved segments were available on 17 patients. Statistical analysis was done using a two tailed, paired t test. SURGICAL METHODS: Decompressive laminectomy was followed by reduction of the spondylolisthesis using intervertebral disc space distraction and pedicle screw instrumentation. The vertebral bodies were supported with bilateral intervertebral lordotic spacers, inserted on their sides and rotated 90 degrees before placing bone graft to either side of them, within the disc space. RESULTS: Mean follow-up time was 21.2 months (range, 12-32 months). No patients were lost to follow-up. Mean preoperative measures of VAS and LBOS of 5.3+/-2.2 and 24.8+/-15.6, respectively, improved to 2.2+/-2.1 (p<.001) and 44.8+/-18.0 (p<.001) at last follow-up. Thirty-one of 34 patients (91%) considered their outcome to be good or excellent. Mean preoperative slip reduced from 20.2% to 1.7% (92% correction, p<.001). Mean focal lordosis increased from 13.1 to 16.1 degrees (26.0% increase, p=.01). There were no device-related procedural complications. Postoperatively, three patients developed an ileus and one a possible deep wound infection, which settled on antibiotics. One patient required extension of his fusion at 12 months for adjacent segment stenosis. CONCLUSIONS: This series suggests that PLIF for degenerative spondylolisthesis using an insert-and-rotate technique can yield high levels of patient satisfaction with low levels of complications and substantial deformity correction using a posterior only approach. Longer-term outcome studies are required regarding the relevance of the restoration of spinal balance.

Adult↗