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PubMed1995

The role of external nonrigid ankle bracing in limiting ankle inversion.

The purpose of this study was to measure the effectiveness of the nonrigid subtalar stabilizer (STS) ankle brace under conditions similar to an unexpected fall that could lead to a lateral ligament injury. The calcaneal inversion angles, times, and ground reaction forces were measured when the subject's right foot, bearing body weight, was suddenly inverted to a side slope of 22 degrees. Thirty subjects, 15 women and 15 men, participated in the study. The overall inversion drop was divided into two phases, free fall and loading. Based on the data of this study it is suggested that the major function of a brace is to restrict the amount of foot inversion during the fall before actual landing occurs rather than functioning as a force bypass for the lateral ligaments during loading after foot contact. The results showed that the brace significantly (p < 0.05) reduced the maximum calcaneal inversion angle from 27.4 +/- 6.1 to 18.3 +/- 6.0 degrees for the overall drop, significantly lengthened the inversion time from 0.14 +/- 0.04 to 0.18 +/- 0.04 s for the overall drop, and significantly reduced the calcaneal peak inversion velocity from 324.6 +/- 111.9 to 165.2 +/- 66.5 degrees/s during loading, and from 278.7 +/- 120.0 to 183.0 +/- 108.7 degrees/s for the overall drop. Following exercise, which incorporated lateral movements and sprinting, the STS ankle brace continued to provide significant (p < 0.05) reduction in the calcaneal inversion angle and velocity, although some of its effectiveness was reduced.(ABSTRACT TRUNCATED AT 250 WORDS)

Accidental Falls↗
PubMed1997

A bioelectric inverse imaging technique based on surface Laplacians.

A new approach is proposed to solve bioelectric inverse problems by employing the surface Laplacian of the bioelectrical potential. A theoretical investigation was conducted to test the feasibility of epicardial inverse imaging of cardiac electrical activity. A two-sphere homogeneous volume conductor model, where the inner sphere represents the epicardium and the outer sphere the body surface, was used. Radial and tangential current dipoles were used to approximate localized wavefronts propagating from the endocardium to the epicardium, and ectopic myocardial activities. The epicardial potential distribution was reconstructed from the body surface Laplacians with the aid of the Tikhonov zero-order regularization technique, which then was compared with the results obtained from the body surface potentials using the same regularization scheme. The two inverse solutions were compared qualitatively via visual inspection of the reconstructed epicardial potential maps, and quantitatively by examining relative errors and correlation coefficients between the "true" and the reconstructed epicardial potentials. Both qualitative and quantitative results indicate that the surface Laplacians play a positive role in improving the ill-posed nature of the bioelectric inverse problem, which would enhance our capability of reconstructing important epicardial events such as extrema in the epicardial potential distribution. The present theoretical study suggests that the Laplacian-based inverse imaging technique may have important applications to epicardial inverse imaging and other bioelectric inverse imaging.

Artifacts↗
PubMed2003

The body-inversion effect.

Researchers argue that faces are recognized via the configuration of their parts. An important behavioral finding supporting this claim is the face-inversion effect, in which inversion impairs recognition of faces more than nonface objects. Until recently, faces were the only class of objects producing the inversion effect for untrained individuals. This study investigated whether the inversion effect extends to human body positions, a class of objects whose exemplars are structurally similar to each other. Three experiments compared the recognition of upright and inverted faces, houses, and body positions using a forced-choice, same/different paradigm. For both reaction time and error data, the recognition of possible human body postures was more affected by inversion than the recognition of houses. Further, the recognition of possible human body postures and recognition of faces showed similar effects of inversion. The inversion effect was diminished for impossible body positions that violated the biomechanical constraints of human bodies. These data suggest that human body positions, like faces, may be processed configurally by untrained viewers.

Adult↗
PubMed2002

On the selection of optimization parameters for an inverse treatment planning replacement of a forward planning technique for prostate cancer.

The influence of organ volume sampling, lateral scatter inclusion, and the selection of objectives and constraints on the inverse treatment planning process with a commercial treatment planning system is investigated and suitable parameters are identified for an inverse treatment planning replacement of a clinical forward planning technique for prostate cancer. For the beam geometries of the forward technique, a variable set of parameters is used for the calculation of dose from pencil beams. An optimal set is identified after the evaluation of optimized plans that correspond to different sets of pencil-beam parameters. This set along with a single, optimized set of objectives and constraints is used to perform inverse planning on ten randomly selected patients. The acceptability of the resulting plans is verified by comparisons to the clinical ones calculated with the forward techniques. For the particular commercial treatment planning system, the default values of the pencil beam parameters are found adequate for inverse treatment planning. For all ten patients, the optimized, single set of objectives and constraints results in plans with target coverage comparable to that of the forward plans. Furthermore inverse treatment planning reduces the overall mean rectal and bladder doses by 4.8% and 5.8% of the prescription dose respectively. The study indicates that (i) inverse treatment planning results depend implicitly on the sampling of the dose distribution, (ii) inverse treatment planning results depend on the method used by the dose calculation model to account for scatter, and (iii) for certain sites, a single set of optimization parameters can be used for all patient plans.

Dose Fractionation, Radiation↗
PubMed2006

Inhibitory effects of benzoate on chiral inversion and clearance of N(G)-nitro-arginine in conscious rats.

N(G)-nitro-arginine (NNA) is known to exhibit stereoselective pharmacokinetics in which N(G)-nitro-d-arginine (d-NNA) has a faster clearance rate than N(G)-nitro-l-arginine (l-NNA) in anesthetized rats, and d-NNA undergoes unidirectional chiral inversion. It was postulated that chiral inversion of d-NNA was performed in a two-step pathway by d-amino acid oxidase (DAAO) followed by an unidentified transaminase. Such chiral inversion contributes (at least partially) to the pharmacokinetic stereoselectivity of NNA. This study used the selective inhibitor of DAAO, sodium benzoate, to test the above hypothesis. An i.v. bolus injection of d-NNA (32 mg/kg) and l-NNA (16 mg/kg) in conscious rats exhibited biphasic disposition with different pharmacokinetic parameters in a stereospecific manner (approximately 5-10-fold differences). Unidirectional chiral inversion of d-NNA but not l-NNA was found from these animals. In addition to its similar inhibitory effects on the d-NNA conversion and DAAO activity in kidney homogenates, sodium benzoate completely blocked chiral inversion of d-NNA and led to a smaller stereospecific difference, reflected by a nearly 50% reduction of d-NNA clearance and a 2-fold increase in t(1/2) and area under the curve of d-NNA in benzoate-pretreated rats. The results suggest that DAAO plays an essential role in chiral inversion of d-NNA and chiral inversion contributes mostly to the pharmacokinetic stereospecificity of NNA.

Animals↗
PubMed2006

Ghrelin receptor inverse agonists: identification of an active peptide core and its interaction epitopes on the receptor.

[D-Arg1,D-Phe5,D-Trp7,9,Leu11]Substance P functions as a low-potency antagonist but a high-potency full inverse agonist on the ghrelin receptor. Through a systematic deletion and substitution analysis of this peptide, the C-terminal carboxyamidated pentapeptide wFwLX was identified as the core structure, which itself displayed relatively low inverse agonist potency. Mutational analysis at 17 selected positions in the main ligand-binding crevice of the ghrelin receptor demonstrated that ghrelin apparently interacts only with residues in the middle part of the pocket [i.e., between transmembrane (TM)-III, TM-VI and TM-VII]. In contrast, the inverse agonist peptides bind in a pocket that extends all the way from the extracellular end of TM-II (AspII:20) across between TM-III and TM-VI/VII to TM-V and TM-IV. The potency of the main inverse agonist could be improved up to 20-fold by a number of space-generating mutants located relatively deep in the binding pocket at key positions in TM-III, TM-IV and TM-V. It is proposed that the inverse agonists prevent the spontaneous receptor activation by inserting relatively deeply across the main ligand-binding pocket and sterically blocking the movement of TM-VI and TM-VII into their inward-bend, active conformation. The combined structure-functional analysis of both the ligand and the receptor allowed for the design of a novel, N-terminally Lys-extended analog of wFwLL, which rescued the high-potency, selective inverse agonism that was dependent upon both AspII:20 and GluIII:09. The identified pharmacophore can possibly serve as the basis for targeted discovery of also nonpeptide inverse agonists for the ghrelin receptor.

Amino Acid Sequence↗
PubMed2000

Potency of ligands correlates with affinity measured against agonist and inverse agonists but not against neutral ligand in constitutively active chemokine receptor.

ORF-74, a 7TM receptor oncogene encoded by human herpes virus 8, shows 50% constitutive activity in stimulating phosphatidylinositol turnover and binds a large variety of CXC chemokines. These endogenous ligands cover a full spectrum of pharmacological properties with growth-related oncogene (GRO)-alpha and -gamma functioning as full agonists; GRObeta as a partial agonist; interleukin (IL)-8, neutrophil-activating peptide (NAP)-2, and epithelial cell-derived activating peptide (ENA)-78 as neutral ligands; granulocyte colony-stimulating factor (GCP)-2 as a partial inverse agonist; and interferon-gamma inducible protein (IP)-10 and stromal cell-derived factor (SDF)-1alpha as full inverse agonists. The affinity for the agonists was independent of whether it was determined in competition binding against the agonist (125)I-GROalpha, against the inverse agonist (125)I-IP-10, or against the neutral ligand (125)I-IL-8. Similarly, the affinities of the inverse agonists were within 1 order of magnitude independent of the choice of radioligand. In contrast, the neutral ligands IL-8, NAP-2, and ENA-78, which all displaced (125)I-IL-8 with single-digit nanomolar affinity showed up to 1000-fold lower affinity against both the radioactive agonist and against the radioactive inverse agonist. A close correlation was observed between the EC(50) values for the ligands and their IC(50) values measured against either radioactive agonist or radioactive inverse agonist, but a poor correlation was found to the IC(50) value measured against the neutral ligand. It is concluded that in ORF-74, ligands compete for binding more according to pharmacological property than to structural homology and that both agonists and inverse agonists, in contrast to neutral ligands, apparently bind with high affinity either to a common conformation of the receptor or to readily interconvertible states, not available for the neutral ligands.

Amino Acid Sequence↗
PubMed2004

Efficacy as a vector: the relative prevalence and paucity of inverse agonism.

This article describes the expected phenotypic behavior of all types of ligands in constitutively active receptor systems and, in particular, the molecular mechanisms of inverse agonism. The possible physiological relevance of inverse agonism also is discussed. Competitive antagonists with the molecular property of negative efficacy demonstrate inverse agonism in constitutively active receptor systems. This is a phenotypic behavior that can only be observed in the appropriate assay; a lack of observed inverse agonism is evidence that the ligand does not possess negative efficacy only if it can be shown that constitutive receptor activity is present. In the absence of constitutive activity, inverse agonists behave as simple competitive antagonists. A survey of 105 articles on the activity of 380 antagonists on 73 biological G-protein-coupled receptor targets indicates that, in this sample dataset, 322 are inverse agonists and 58 (15%) are neutral antagonists. The predominance of inverse agonism agrees with theoretical predictions which indicate that neutral antagonists are the minority species in pharmacological space.

Animals↗
PubMed2006

Influence of head models on EEG simulations and inverse source localizations.

BACKGROUND: The structure of the anatomical surfaces, e.g., CSF and gray and white matter, could severely influence the flow of volume currents in a head model. This, in turn, will also influence the scalp potentials and the inverse source localizations. This was examined in detail with four different human head models. METHODS: Four finite element head models constructed from segmented MR images of an adult male subject were used for this study. These models were: (1) Model 1: full model with eleven tissues that included detailed structure of the scalp, hard and soft skull bone, CSF, gray and white matter and other prominent tissues, (2) the Model 2 was derived from the Model 1 in which the conductivity of gray matter was set equal to the white matter, i.e., a ten tissue-type model, (3) the Model 3 was derived from the Model 1 in which the conductivities of gray matter and CSF were set equal to the white matter, i.e., a nine tissue-type model, (4) the Model 4 consisted of scalp, hard skull bone, CSF, gray and white matter, i.e., a five tissue-type model. How model complexity influences the EEG source localizations was also studied with the above four finite element models of the head. The lead fields and scalp potentials due to dipolar sources in the motor cortex were computed for all four models. The inverse source localizations were performed with an exhaustive search pattern in the motor cortex area. The inverse analysis was performed by adding uncorrelated Gaussian noise to the scalp potentials to achieve a signal to noise ratio (SNR) of -10 to 30 dB. The Model 1 was used as a reference model. RESULTS: The reference model, as expected, performed the best. The Model 3, which did not have the CSF layer, performed the worst. The mean source localization errors (MLEs) of the Model 3 were larger than the Model 1 or 2. The scalp potentials were also most affected by the lack of CSF geometry in the Model 3. The MLEs for the Model 4 were also larger than the Model 1 and 2. The Model 4 and the Model 3 had similar MLEs in the SNR range of -10 dB to 0 dB. However, in the SNR range of 5 dB to 30 dB, the Model 4 has lower MLEs as compared with the Model 3. DISCUSSION: These results indicate that the complexity of head models strongly influences the scalp potentials and the inverse source localizations. A more complex head model performs better in inverse source localizations as compared to a model with lesser tissue surfaces. The CSF layer plays an important role in modifying the scalp potentials and also influences the inverse source localizations. In summary, for best results one needs to have highly heterogeneous models of the head for accurate simulations of scalp potentials and for inverse source localizations.

Adult↗
PubMed1997

Relationship between the metabolic chiral inversion and chemical structure of 4-phenyl-4-oxobutanoic acids, derivatives of anti-rheumatic agent KE-298.

The relationship between metabolic chiral inversion and chemical structure of various 4-phenyl-4-oxobutanoic acids (4-OBA), derivatives of anti-rheumatic agent KE-298 [2-acetylthiomethyl-4-(4-methylphenyl)-4-oxobutanoic acid], was investigated in rats. Chiral inversion occurred with the thio-alkyl group, whereas the thio-acyl group played no role in the inversion of 4-OBA. A 2-methylene moiety was required for the inversion. When the 4-carbonyl moiety was removed, chiral inversion was significantly decreased, which provided an affinity for the intramitochondrial medium chain fatty acid CoA ligase. In addition, the distance between the chiral center and the carbonyl moiety was also an important factor for chiral inversion. While a sulfur atom was not indispensable for the chiral inversion, the existence of the sulfur atom influenced its affinity to the long chain fatty acid CoA ligase.

Animals↗
PubMed2006

Single-shot inversion recovery TrueFISP for assessment of myocardial infarction.

OBJECTIVE: The aim of the study was to assess the diagnostic accuracy of imaging the myocardium with a fast multislice inversion recovery 2D single-shot true fast imaging with steady-state precession (trueFISP) sequence during a single breath-hold in comparison with an established segmented inversion recovery turbo fast low-angle shot (turboFLASH) sequence. SUBJECTS AND METHODS: Forty-three patients with myocardial infarction were examined on a 1.5-T MR system 10 min after administration of contrast material (gadodiamide, 0.2 mmol/kg) with a single-shot 2D multislice technique (single-shot inversion recovery trueFISP) that allows one to image the entire short axis during one breath-hold (18 heartbeats) and with a segmented 2D single-slice technique (inversion recovery turboFLASH) that requires one breath-hold per slice (12 heartbeats). Signal intensity was determined in normal myocardium, in infarcted myocardium, and in the left ventricle. The contrast-to-noise ratio (CNR) of normal and infarcted myocardium was determined. The areas of hyperintense infarctions on selected slices and the entire volumes were compared for both sequence techniques. RESULTS: The inversion recovery trueFISP sequence has a lower CNR than the inversion recovery turboFLASH sequence (mean values, 10.0 vs 12.9, respectively; p = 0.005) for differentiation of viable from nonviable myocardium. The CNR of injured myocardium and blood in the left ventricular cavity also has a lower value for the multislice technique compared with the single-slice technique (0.6 vs 1.2, respectively; p = 0.045). Assessment of the area of infarction within one slice (r = 0.97, p < 0.002) and of the volume of the entire infarction (r = 0.96, p < 0.003) is possible with excellent correlation of both techniques. CONCLUSION: Despite having a lower CNR, the inversion recovery 2D single-shot trueFISP sequence allows fast and accurate identification of the area and volume of infarction with high spatial resolution within a single breath-hold.

Adult↗
PubMed2003

Diagnostic accuracy of phase-inversion tissue harmonic imaging versus fundamental B-mode sonography in the evaluation of focal lesions of the kidney.

OBJECTIVE: We compared phase-inversion tissue harmonic imaging with fundamental B-mode sonography in the evaluation of focal lesions of the kidney. SUBJECTS AND METHODS: For our prospective study, 114 patients underwent sonography of the kidneys in both modes, fundamental B-mode sonography and phase-inversion tissue harmonic imaging, in a randomly chosen scanning order. Imaging parameters were standardized. Sonographic diagnoses were made under real-time conditions by the examining radiologist. All sonographic diagnoses were compared with a diagnostic reference modality: contrast-enhanced CT, contrast-enhanced MR imaging, or histopathology. Three radiologists different from the examiners evaluated overall image quality, lesion conspicuity, and fluid-solid differentiation for both modalities using hard-copy images. RESULTS: In 70 patients, fundamental B-mode sonography as the first technique depicted 73 of 111 lesions 10 mm or larger and enabled 71 lesions to be correctly characterized (sensitivity, 65.8%; accuracy, 64.0%). As the first mode, phase-inversion tissue harmonic imaging depicted 57 of 65 focal lesions and enabled 54 lesions to be accurately classified in 44 patients (sensitivity, 87.7%; accuracy, 83.1%). The differences in sensitivity and accuracy were statistically significant (95% confidence interval). For overall image quality, lesion conspicuity, and fluid-solid differentiation phase-inversion harmonic imaging was superior to fundamental B-mode sonography (p < 0.0001). CONCLUSION: Phase-inversion tissue harmonic imaging is superior to fundamental B-mode sonography in the sonography of focal kidney lesions because phase-inversion tissue harmonic imaging has better overall image quality, lesion conspicuity, and fluid-solid differentiation. In six cases, phase-inversion tissue harmonic imaging added crucial diagnostic information that changed patient management.

Adult↗
PubMed1991

Rapid inversion of dominance relationship matrices for noninbred populations by including sire by dam subclass effects.

For estimation of dominance effects and dominance variance, the inverse of a dominance relationship matrix is required. Dominance effects can be partitioned into sire x dam or sire x maternal grandsire subclass effects that are inherited and residuals within subclass that are not inherited. The subclass effects have immediate use in predicting performance of offspring from prospective matings. A rapid method for directly computing the inverse relationship matrix of subclass effects is presented. The procedure is similar to Henderson's simple method of computing an inverse additive genetic relationship matrix. The inverse relationship matrix among subclass effects consists of a contribution from each subclass of coefficients of a matrix of maximum size 9 x 9. The algorithm can be modified to compute the inverse of the relationship matrix among sire x dam or sire x maternal grandsire subclasses and among individual dominance effects. Computing cost increases approximately linearly with dimensions of inverses. Dimensions could be several times the number of subclasses in the data because subclasses without records but providing relationship ties must be added. Computation of the inverse relationship matrix among 136,827 sire x maternal grandsire subclasses in a population of 765,868 animals required 163 central processing unit seconds on an IBM 3090 and less than 4 Mbytes of memory.

Algorithms↗
PubMed1999

Novel actions of inverse agonists on 5-HT2C receptor systems.

In cell systems where ligand-independent receptor activity is optimized (such as when receptors are overexpressed or mutated), acute treatment with inverse agonists reduces basal effector activity whereas prolonged exposure leads to sensitization of receptor systems and receptor up-regulation. Few studies, however, have reported effects of inverse agonists in systems where nonmutated receptors are expressed at relatively low density. Here, we investigated the effects of inverse agonists at human serotonin (5-HT)2C receptors expressed stably in Chinese hamster ovary cells ( approximately 250 fmol/mg protein). In these cells, there is no receptor reserve for 5-HT and 5-HT2C inverse agonists did not reduce basal inositol phosphate (IP) accumulation nor arachidonic acid (AA) release but behaved as simple competitive antagonists, suggesting that these receptors are not overexpressed. Prolonged treatment (24 h) with inverse agonists enhanced selectively 5-HT2C-mediated IP accumulation but not AA release. The enhancing effect occurred within 4 h of treatment, reversed within 3 to 4 h (after 24-h treatment), and could be blocked with neutral antagonists or weak positive agonists. The enhanced responsiveness was not due to receptor up-regulation but may involve changes in the expression of the G protein, Galphaq/11 and possibly Galpha12 and Galpha13. Interestingly, 24-h exposure to inverse agonists acting at 5-HT2C receptors also selectively enhanced IP accumulation, but not AA release, elicited by activation of endogenous purinergic receptors. These data suggest that actions of inverse agonists may be mediated through effects on receptor systems that are not direct targets for these drugs.

Animals↗
PubMed2001

Inverse agonist actions of typical and atypical antipsychotic drugs at the human 5-hydroxytryptamine(2C) receptor.

Atypical antipsychotic drugs, which are distinguished from typical antipsychotic drugs by a lower incidence of extra-pyramidal side effects and less propensity to elevate serum prolactin levels (e.g., clozapine, olanzapine, risperidone, quetiapine, ziprasidone), have become the most widely used treatments for schizophrenia, although their precise mechanism of action remains controversial. It has been suggested that this group of atypical antipsychotic drugs is characterized by preferentially high affinities for 5-hydroxytryptamine (5-HT)2A serotonin receptors and relatively low affinities for D2-dopamine receptors. It has recently been proposed that these atypical antipsychotic drugs may also be distinguished from typical antipsychotic drugs (e.g., haloperidol, fluphenazine, chlorpromazine, and so on) by inverse agonist actions at the 5-HT2C-INI RNA edited isoform of the human 5-HT2C receptor transiently expressed in COS-7 cells. We have examined the relationship among 5-HT2C inverse agonist potency, efficacy, and atypical antipsychotic drug status in HEK-293 cells of a large number of typical and atypical antipsychotic drugs using human embryonic kidney (HEK)-293 cells stably transfected with the h5-HT2C-INI receptor. Inverse agonist actions at h5-HT2C-INI receptors were measured for both typical and atypical antipsychotic drugs. Thus, some typical antipsychotic drugs (chlorpromazine, mesoridazine, fluphenazine, and loxapine) were efficient inverse agonists, whereas several clinically effective atypical antipsychotic drugs (remoxapride, quetiapine, sulpiride, melperone, amperozide) were not. Additionally, several drugs without significant antipsychotic actions (M100907, ketanserin, mianserin, ritanserin, and amitriptyline) were potent inverse agonists at the 5-HT2C-INI isoform expressed in HEK-293 cells. Taken together, these results demonstrate that both typical and atypical antipsychotic drugs may exhibit inverse agonist effects at the 5-HT2C-INI isoform of the human 5-HT2C receptor and that no relationship exists between inverse agonist actions and atypicality.

3T3 Cells↗
PubMed1977

Isolated ventricular inversion with double inlet left ventricle.

2 patients with viscero-atrial situs solitus, isolated ventricular inversion (IVI) and double inlet right-sided morphologic left ventricle are presented. Isolated ventricular inversion is a rare cardiac anomaly characterized by ventricular inversion, subpulmonary conus, and ventriculo-arterial concordance. Their angiocardiographic and pathologic features are presented, and the morphologic findings of the 9 patients in the literature with isolated ventricular inversion are reviewed. Of the 11 known patients with isolated ventricular inversion, levocardia was present in 10 and dextrocardia in 1; viscero-atrial situs solitus in 9 and inversus in 2; L-ventricular loop in 9 and D-loop in 2. The atrial septum was intact in 4. An intact ventricular septum was noted in only 2 patients while in 3, more than one ventricular septal defects were present, and 2 patients exhibited morphologic single ventricle. A solitary ventricular septal defect was noted in the remainder. Significant tricuspid valve abnormalities, including atresia, stenosis or hypoplasia with supravalvular fibrous ring were found in 7 patients. In 2 of these, both with significant obstruction at the tricuspid valve, both atrioventricular valves emptied into the morphologic left ventricle--thus isolated ventricular inversion with double inlet left ventricle. Pulmonary outflow tract obstruction was evident in only 3 patients. Total anomalous pulmonary venous return occurred twice and right juxtaposition of the atrial appendages once. Thus, while the patient with isolated ventricular iversion may present with clinical and hemodynamic features characteristic of classical transposition physiology the high frequency of significant associated anomalies would complicate this. Finally, the anomaly must be differentiated from the levo-transposition, isolated atrial inversion, and the anatomically corrected malpositions.

Adult↗
PubMed1988

Exercise during gravity inversion: acute and chronic effects.

The purpose of this study was to determine whether gravity inversion could correctly be called an exercise, and whether inversion and inverted exercise produced safe blood pressure responses. Systolic blood pressure (SBP), diastolic blood pressure (DBP), heart rate (HR), and oxygen consumption (VO2) were measured in 19 healthy young men (means = 20.31 years) in seven positions: (1) standing passive (STD), (2) inverted passive (INV), (3) standing recovery postpassive inversion (SRPI), (4) standing exercise (SDE), (5) standing recovery poststanding exercise (SRPSE), (6) inverted exercise (INVE), and (7) inverted recovery postinverted exercise (IRPIE). Ten of the subjects participated in a five-week inversion training program, after which all 19 subjects were retested. Compared to STD, INV elicited significant increases in SBP/DBP and a significant decrease in HR. The average INV blood pressure was 146/97 mmHg, which was further increased during INVE to 158/101 mmHg. These responses increase the workload of the heart and may be dangerous to some populations. No physiologic adaptations occurred in any of the inverted positions as a result of inversion training. Gravity inversion should not be compared to or classified as an exercise. Some previously suggested inverted exercises are not recommended. Because of the nature of the responses, medical screening before the use of inversion devices is critical.

Adult↗
PubMed1996

Inversion polymorphism in natural populations of Drosophila bipectinata.

Inversion polymorphism was studied in seven natural populations of Drosophila bipectinata, five from northern and two from southern India. Chromosomal analysis of these populations revealed the presence of three paracentric inversions which are widespread in populations of D. bipectinata. Quantitative data indicated that the frequency of inversions and the level of inversion heterozygosity were very low in populations of D. bipectinata. There is no evidence for genetic differentiation between populations as a result of inversion polymorphism. These findings provide evidence for rigid chromosomal polymorphism in D. bipectinata. Significant non-random associations between inversions indicated epistatic interaction between inversions in natural populations of D. bipectinata.

Age Factors↗