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K Krajnak

Publications and source records attributed to K Krajnak.

11 recordsLinked to original sources
PubMed2005

Acute vibration increases alpha2C-adrenergic smooth muscle constriction and alters thermosensitivity of cutaneous arteries.

The vascular symptoms of hand-arm vibration syndrome, including cold-induced vasospasm, are in part mediated by increased sensitivity of cutaneous arteries to sympathetic stimulation. The goal of the present study was to use a rat tail model to analyze the effects of vibration on vascular function and alpha-adrenoceptor (AR) responsiveness. Rats were exposed to a single period of vibration (4 h, 125 Hz, constant acceleration 49 m/s2 root mean square). The physical or biodynamic response of the tail demonstrated increased transmissibility or resonance at this frequency, similar to that observed during vibration of human fingers. Morphological analysis demonstrated that vibration did not appear to cause structural injury to vascular cells. In vitro analysis of vascular function demonstrated that constriction to the alpha1-AR agonist phenylephrine was similar in vibrated and control arteries. In contrast, constriction to the alpha2-AR agonist UK14304 was increased in vibrated compared with control arteries, both in endothelium-containing or endothelium-denuded arteries. The alpha2C-AR antagonist MK912 (3 x 10(-10) M) inhibited constriction to UK14304 in vibrated but not control arteries, reversing the vibration-induced increase in alpha2-AR activity. Moderate cooling (to 28 degrees C) increased constriction to the alpha2-AR agonist in control and vibrated arteries, but the magnitude of the amplification was less in vibrated compared with control arteries. Endothelium-dependent relaxation to acetylcholine was similar in control and vibrated arteries. Based on these results, we conclude that a single exposure to vibration caused a persistent increase in alpha2C-AR-mediated vasoconstriction, which may contribute to the pathogenesis of vibration-induced vascular disease.

Adrenergic alpha-Agonists↗
PubMed2005

Analysis of the dynamic strains in a fingertip exposed to vibrations: Correlation to the mechanical stimuli on mechanoreceptors.

The reduction in vibrotactile sensitivity in the fingertip is assumed to be associated with the exposure of the tissues to repetitive, non-physiological strains during dynamic loading. Experimental results demonstrated that the magnitude of a vibration-induced temporary threshold shift is dependent upon the vibration frequency of both the exposure and testing stimuli. In the present study, the frequency-dependent strain imposed on cutaneous and subcutaneous tissues of the fingertip is analyzed theoretically using a finite element model. The proposed fingertip model is two-dimensional and includes major anatomical substructures: skin, subcutaneous tissue, bone, and nail. The soft tissues (skin and subcutaneous tissues) were assumed to be nonlinearly elastic and viscoelastic, while the bone and nail were considered as linearly elastic. Simulations were performed for the contact between the fingertip and a flat surface for four different pre-compressions (0.5, 1.0, 1.5, and 2.0 mm). The frequency-dependent distributions of the dynamic strain magnitudes in the soft tissues were investigated. The model predictions indicated that the vibration exposure at a frequency range from 63 to 250 Hz will induce excessive dynamic strain in the deep zone of the finger tissues, effectively inhibiting the high-frequency mechanoreceptors; while the vibration exposure at low frequency (less than 31.5 Hz) tends to induce excessive dynamic strain in superficial layer in the tissues, inhibiting the low-frequency mechanoreceptors. These theoretical predictions are consistent with the experimental observations in literature. The proposed model can be used to predict the responses of the soft tissues in different depths to vibration exposures, providing valuable information and data that are essential for improving vibrotactile perception tests.

Fingers↗
PubMed2001

Fos-induction in gonadotropin-releasing hormone neurons receiving vasoactive intestinal polypeptide innervation is reduced in middle-aged female rats.

A hallmark of reproductive aging in rats is a delay in the initiation and peak, and a decrease in the amplitude, of both proestrous and steroid-induced surges of LH and a decrease in the number of GnRH neurons that express Fos during the surge. The altered timing of the LH surge and the decline in Fos expression in GnRH neurons may be due to changes in the rhythmic expression of vasoactive intestinal polypeptide (VIP), a neuropeptide that carries time-of-day information from the circadian pacemaker, located in the suprachiasmatic nuclei (SCN), to GnRH neurons. The goals of our study were to determine if aging alters 1) the innervation of GnRH neurons by VIP and 2) the ability of VIP to activate GnRH neurons by examining the effects of aging on the number of GnRH neurons apposed by VIP fibers and the number of GnRH neurons that receive VIP input that express Fos. Immunocytochemistry for GnRH and VIP; or GnRH, VIP, and Fos was performed on tissue sections collected from young (2-4 mo), regularly cycling females and middle-aged (10-12 mo) females in constant estrus. The number of GnRH neurons, GnRH neurons apposed by VIP fibers, and GnRH neurons that express Fos and apposed by VIP fibers were counted in both age groups. Our results clearly demonstrate that aging does not alter the number of GnRH neurons that receive VIP innervation. However, the number of GnRH neurons that receive VIP innervation and coexpress Fos decreases significantly. We conclude that the age-related delay in the timing of the LH surge is not due to a change in VIP innervation of GnRH neurons, but instead may result from a decreased sensitivity of GnRH neurons to VIP input.

Aging↗
PubMed1998

Aging alters the rhythmic expression of vasoactive intestinal polypeptide mRNA but not arginine vasopressin mRNA in the suprachiasmatic nuclei of female rats.

Our laboratory has shown that the ability of the suprachiasmatic nuclei (SCN) to regulate a number of rhythmic processes may be compromised by the time females reach middle age. Therefore, we examined the effects of aging on the rhythmic expression of two neuropeptides synthesized in the SCN, vasoactive intestinal polypeptide (VIP) and arginine vasopressin (AVP), using in situ hybridization. Because both VIP and AVP are outputs of the SCN, we hypothesized that age-related changes in rhythmicity are associated with alterations in the patterns of expression of these peptides. We found that VIP mRNA levels exhibited a 24 hr rhythm in young females, but by the time animals were middle-aged, this rhythm was gone. The attenuation of rhythmicity was associated with a decline in the level of mRNA per cell and in the number of cells in the SCN producing detectable VIP mRNA. AVP mRNA also showed a robust 24 hr rhythm in young females. However, in contrast to VIP, the AVP rhythm was not altered in the aging animals. The amount of mRNA per cell and the number of cells expressing AVP mRNA also was not affected with age. Based on these results we conclude that (1) various components of the SCN are differentially affected by aging; and (2) age-related changes in various rhythms may be attributable to changes in the ability of the SCN to transmit timing information to target sites. This may explain why the deterioration of various rhythmic processes occurs at different rates and at different times during the aging process.

Aging↗
PubMed1998

Sex differences in the daily rhythm of vasoactive intestinal polypeptide but not arginine vasopressin messenger ribonucleic acid in the suprachiasmatic nuclei.

The timing of the preovulatory surge of LH in female rodents is tightly coupled to the environmental light/dark cycle. This coupling is mediated by the circadian pacemaker located in the suprachiasmatic nuclei (SCN). Studies indicate that vasoactive intestinal polypeptide (VIP) and arginine vasopressin (AVP), which are synthesized in the SCN, transmit circadian information from the SCN to GnRH neurons, thereby regulating the timing of the LH surge. However, to date, the rhythmic expression of these two peptides in the SCN has only been examined in males. The pattern of VIP expression in males is difficult to reconcile with its role in the LH surge. The purpose of the present study was to assess the rhythm of VIP messenger RNA (mRNA) levels in the SCN of female rats under several endocrine conditions. We compared this rhythm to that in males and to AVP mRNA rhythms in all experimental groups. In all groups of females, VIP mRNA levels were rhythmic, with peak expression occurring during the light phase and a nadir occurring during the dark phase. The rhythm was approximately 12 h out of phase compared with that in males. The rhythmic expression of AVP mRNA in the SCN was virtually identical in all groups of animals. Based on these results, we conclude that 1) the rhythm of VIP seen in the SCN of females during the day may serve as a facilitory signal from the SCN to GnRH neurons; 2) the sex-specific pattern of VIP mRNA does not depend on estradiol; and 3) AVP gene expression within the SCN is not sexually differentiated or altered by estradiol.

Animals↗
PubMed1997

The induction of Fos-like proteins in the suprachiasmatic nuclei and intergeniculate leaflet by light pulses in degus (Octodon degus) and rats.

In nocturnal rodents, exposure to light results in an increase in Fos expression in two regions that receive direct retinal input: the suprachiasmatic nuclei (SCN) of the hypothalamus and the intergeniculate leaflet (IGL) of the thalamus. The induction of Fos within the SCN of nocturnal rodents is phase dependent, with light presented during the subjective night increasing Fos expression and light presented during the subjective day having little effect. By contrast, Fos expression increases in the IGL when light is presented during the subjective day or night. It is unclear whether Fos is part of the pathway mediating light-induced phase shifts in diurnal rodents. In the present study, the ability of light to induce immunostaining for Fos in the SCN and IGL was compared in diurnal rodents, Octodon degus (degus), and nocturnal rats. Degus and rats were either maintained in constant darkness or exposed to a 1-h light pulse at circadian time (CT) 4 or 16. Degus exhibit robust phase shifts at each of those circadian hours, whereas rats demonstrate phase shifts only at CT 16. In degus, exposure to a 1-h light pulse at CT 16 resulted in an increase in the number of Fos-immunopositive (Fos+) cells in the ventrolateral SCN. By contrast, a 1-h light pulse at CT 4 resulted in a decrease in the number of Fos+ cells in the dorsomedial portion of the SCN. In rats, a light pulse presented at CT 16 resulted in an increase in Fos+ cells throughout the SCN, and a pulse at CT 4 had no effect on Fos staining. Both degus and rats showed increases in Fos expression in the IGL after light exposure at CTs 4 and 16. The authors conclude that light pulses presented at times that produce phase shifts in activity rhythms also alter Fos expression in the SCN and IGL of degus. Although these effects of light exposure on Fos expression are not identical in diurnal and nocturnal rodents, it is likely that Fos and other immediate early genes are part of the pathway mediating the effects of light in both diurnal and nocturnal rodents.

Animals↗
PubMed1996

Short-photoperiod exposure reduces L-aromatic-amino-acid decarboxylase immunostaining in the arcuate nucleus and median eminence of male Syrian hamsters.

In male hamsters, exposure to short photoperiod (SD) results in a decrease in median eminence and posterior pituitary dopamine (DA) concentrations. To determine if the SD-induced decline in DA is due to a decrease in the number of neurons synthesizing DA, immunocytochemistry was used to identify cells containing tyrosine hydroxylase (TH) and L-aromatic amino acid decarboxylase (AADC) in animals housed under long photoperiod (LD) or SD. Immunopositive cells were counted in the arcuate and caudal periventricular nuclei, regions where the DA neurons that project to the median eminence and posterior pituitary are located. AADC immunopositive (AADC +) cells were also counted in the median eminence. Photoperiod did not affect the number of TH immunopositive (TH+) or AADC + cells in the caudal periventricular nuclei. In the arcuate nuclei, SD exposure did not affect the number of TH+ neurons, but produced a significant decline in the number of AADC + cells. The number of AADC + cells was also reduced in the median eminence of SD-exposed animals. This decline in AADC+ cells may play a role in SD-induced changes in hypothalamic regulation of anterior pituitary hormone release, including the decline in median eminence DA concentrations.

Animals↗
PubMed1995

Seasonal changes in median eminence dopamine in male Syrian hamsters: role of the gonads and duration of exposure to short days.

Median eminence dopamine concentrations are reduced in male hamsters housed in a short photoperiod for 12 weeks, but tyrosine hydroxylase activity and dopamine metabolism are unaffected. The mechanism responsible for this decrease in dopamine is unclear. The purpose of the experiments presented here was to examine the effects of gonadal steroids on this decline in median eminence dopamine concentrations, and to characterize the time course over which this change occurs. Experiment 1 examined the effects of short day exposure on median eminence dopamine concentrations and tuberoinfundibular dopamine neuronal activity (i.e., accumulation of 3,4-dihydroxyphenylanine) in castrated male hamsters. The results of that experiment suggest that the short-day induced decline in median eminence dopamine concentrations is maintained in the absence of gonadal steroids. In Experiments 2 and 3, tuberoinfundibular dopamine neuronal activity (accumulation of 3,4-dihydroxyphenylalanine and 3,4-dihydroxyphenylacetic acid concentrations, respectively), median eminence dopamine concentrations and circulating prolactin levels were measured in animals housed in short days for varying lengths of time. This was done to determine when the decline in median eminence dopamine concentrations occurs and if the decline is preceded by a change in tuberoinfundibular dopamine neuronal activity. The results of these two experiments suggest that median eminence dopamine concentrations and circulating prolactin levels decline after approximately 4 weeks of short-day exposure, and that these photoperiod induced changes are not associated with changes in tuberoinfundibular dopaminergic neuronal activity.

3,4-Dihydroxyphenylacetic Acid↗
PubMed1994

The effect of short-photoperiod exposure on tuberoinfundibular dopamine neurons in male and female Syrian hamsters.

In male hamsters, exposure to a short photoperiod results in a significant decrease in median eminence (ME) dopamine (DA) concentrations. The mechanism responsible for this decrease in DA is unknown. The experiments described in this paper were designed to examine the effects of photoperiod on DA metabolism and synthesis in the ME to determine if a change in these processes is responsible for the short-photoperiod-induced decrease in ME DA concentrations. In the first experiment, the metabolism of DA in tuberoinfundibular dopamine (TIDA) neuronal terminals was determined by measuring ME concentrations of 3,4-dihydroxyphenylacetic acid (DOPAC; a major metabolite of DA) and DA in male and female hamsters housed in long and short photoperiods. In both males and females, exposure to the short photoperiod induced a collapse of the reproductive system and a reduction in circulating prolactin. In males, but not in females, exposure to the short photoperiod reduced ME DA concentrations; however, DOPAC concentrations were not affected by photoperiod. Thus, the decrease in ME DA seen in males is not the result of an increase in DA metabolism. In the second experiment, tyrosine hydroxylase (TH) activity in the ME of males was determined by injecting animals housed in long and short photoperiods with a L-aromatic amino acid decarboxylase inhibitor (NSD 1015) and measuring 3,4-dihydroxyphenylalanine (DOPA). Consistent with Experiment 1, ME DA concentrations were significantly decreased in gonadally regressed males housed in a short photoperiod; however, ME DOPA accumulation was not affected. Thus, the observed decrease in DA is not the result of a decrease in TH activity in the ME. The results of the experiments presented here indicate that (1) in males but not females, the decrease in circulating prolactin seen in animals housed in a short photoperiod for 12 weeks is associated with a decrease in ME DA concentrations, and (2) the decrease in ME DA seen in males housed in a short photoperiod is not the result of an increase in DA metabolism or a decrease in synthesis by TIDA neurons.

3,4-Dihydroxyphenylacetic Acid↗