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Identification and distribution of neurons presumed to give rise to cerebellar climbing fibers in turtle. A retrograde axonal flow study using radioactive D-aspartate as a marker.

Radioactive D-aspartate and horseradish peroxidase were injected into the cerebellar cortex in turtle, Pseudemys scripta elegans. While neurons retrogradely labeled with horseradish peroxidase were found in various regions of the spinal cord and brainstem, labeled cells following aspartate injections were only observed in circumscribed regions of the caudal medulla. In rat it was recently reported that climbing fibers, but no other cerebellar afferents, were retrogradely labeled with D-aspartate (Wiklund et al.12). It is suggested that the aspartate-positive neurons in turtle also give rise to climbing fibers.

Afferent Pathways↗

Visual activity in the telencephalon of the painted turtle, Chrysemys picta.

Multiple unit activity in response to visual stimulation was recorded in the following telencephalic areas of the painted turtle: lateral and medial divisions of the dorsal cortex, lateral and medial divisions of the dorsal ventricular ridge, and the striatum. The data confirm anatomical evidence for ascending visual input to the dorsal cortex, the lateral dorsal ventricular ridge and the striatum. The identification of a new visual zone in a medial division of the dorsal ventricular ridge suggests that turtles, and perhaps other reptiles, possess at least 3 visual pallial areas.

Animals↗

Chemical synapses between turtle photoreceptors.

Rod photoreceptors of the snapping turtle retina wer Golgi impregnated and studied in the electron microscope. Telodendria arising from the synaptic bases ended at rods and cones as lateral or central elements of the ribbon synaptic complex, thus providing clear evidence of chemical synapses between turtle photoreceptors.

Animals↗

Choline acetyltransferase-like immunoreactivity in the forebrain of the red-eared pond turtle (Pseudemys scripta elegans).

Choline acetyltransferase (ChAT) immunohistochemistry was used to map the cholinergic neurons in the forebrain of Pseudemys turtles. Cell bodies with ChAT-like immunoreactivity were seen in the septum, the nucleus of the diagonal band, and embedded within the medial and lateral forebrain bundles. The region of the medial and lateral forebrain bundles contained the greatest concentration of ChAT-positive neurons. Virtually no ChAT-like immunoreactivity was seen in the areas composing the reptilian homologue of the mammalian striatum. It is suggested that the turtle basal forebrain cholinergic neurons may represent the evolutionary precursors to the mammalian cholinergic neurons of the basal forebrain and even the striatum.

Acetylcholinesterase↗

Tyrosine hydroxylase immunohistochemistry fails to demonstrate dopaminergic interplexiform cells in the turtle retina.

A number of catecholaminergic, presumably dopaminergic, cells could be observed in the turtle retina, because of their tyrosine hydroxylase immunoreactivity. They were amacrine cells with a pear-shaped soma and dendrites distributed in 3 sublayers within the inner plexiform layer. Neither sclerally directed TH-positive processes nor terminals in the outer plexiform layer were observed, suggesting that dopaminergic interplexiform cells do not exist in the turtle retina.

Animals↗

Somatostatin and neuropeptide Y are almost exclusively found in the same neurons in the telencephalon of turtles.

In mammals, somatostatin and neuropeptide Y (NPY) are largely found in the same neurons of the telencephalon. To determine if this is a phylogenetically ancient feature of telencephalic organization, the brain of red-eared turtles was examined using immunofluorescence double-labeling procedures. The results showed that somatostatin and NPY are found almost exclusively in the same neurons in the telencephalon of turtles, but these neuropeptides rarely co-occur in neurons outside the telencephalon. Thus, the extensive co-occurrence of NPY and somatostatin appears to be a feature of telencephalic organization that was present in the reptilian common ancestors of mammals and modern reptiles.

Animals↗

Lateralization of opioid receptors in turtle visual cortex.

The opioid mu-agonist morphine, the delta-agonist [D-Ala2,D-Leu5]enkephalin (DADL) and the kappa-agonist bremazocine locally applied to the surface of turtle visual cortex inhibited the orthodromic evoked potential (EP; fast negative component N1). After application of the sigma-agonist SKF 10.047 the inhibition was followed by facilitation of EP. The lack of cross-desensitization to the inhibitory action of opioids upon EP indicates that the drugs exert their effects via different opioid receptors. Bremazocine and morphine predominantly inhibited the left cortical EP, whereas DADL was a potent inhibitor of the right cortical EP. Thus, the opioid receptors which modulate evoked electrical activity of the left visual cortex (LVC) apparently belong mostly to the kappa- and mu-type, while delta-receptors were predominantly responsible for the modulation of electrical activity in the right visual cortex (RVC). Besides, we have studied in vivo binding of the kappa-agonist [3H]ethylketocyclazocine ([3H]EKC) and the delta-agonist [3H]DADL to LVC and RVC. The binding was specific and could be accounted for by the interaction with membrane opioid receptors and/or specific uptake of these drugs by cortex cells. [3H]EKC and [3H]DADL exhibited a more effective binding to LVC and RVC membranes, respectively. The results obtained in vitro apparently indicate that LVC and RVC differ in the number of kappa- and delta-binding sites. Thus, turtle brain may have a side-specific mechanism for selective neurochemical regulation of neuron activity in LVC and RVC realized predominantly via kappa- and delta-receptors, respectively.

Animals↗

Episodic respiratory related discharge in turtle cranial motoneurons: in vivo and in vitro studies.

An in vitro brainstem-spinal cord preparation from adult turtles was used to study mechanisms underlying the episodic breathing pattern in poikilothermic vertebrates. The preparation (1) generates a stable, episodic burst pattern in cranial motoneuron discharge lasting several days; and (2) is similar to discharge patterns in vivo that are synchronous with respiratory airflow. Episodic breathing in reptiles appears to be intrinsic to the CNS in turtles, and does not require oscillations in afferent feedback.

Action Potentials↗

Cholinergic and GABAergic neurons occur in both the distal and proximal turtle retina.

Turtle retinas were processed immunocytochemically and histochemically to detect the presence of choline acetyltransferase (ChAT), acetylcholinesterase (AChE), and glutamate decarboxylase (GAD). We observed cholinergic and gamma-aminobutyric acid (GABA)ergic neurons in the proximal retina, as expected, and in the distal retina as well. ChAT immunoreactivity in the distal retina was observed within the axons and pedicles of numerous cone photoreceptors, suggesting that a population of turtle cone photoreceptors uses ACh as a neurotransmitter. Type L2 horizontal cells were immunoreactive for GAD, and their dendrites invaginated into cone pedicles. AChE histochemistry revealed processes within the outer plexiform layer which formed a loosely organized lattice. In the proximal retina, labeling for ChAT and GAD was similar to that reported by previous investigators. Processes from ChAT-labeled amacrine cells in the inner nuclear layer formed a stratum within the distal inner plexiform layer (IPL) (at 16-21% relative IPL depth), and processes from ChAT-labeled amacrines in the ganglion cell layer formed a proximal ChAT stratum (at 55-58% relative IPL depth). In addition, six AChE-labeled bands and five GAD-labeled bands were observed within the IPL of stained retinas. Therefore, we determined that the two broadest AChE-labeled bands and the two broadest GAD-labeled bands overlapped the two labeled ChAT strata. The evidence for cholinergic and GABAergic processes in both the inner plexiform layer and the outer plexiform layer, combined with electrophysiological evidence from other investigators, raises the possibility that distal retinal neurons may be involved in the encoding of directional information.

Acetylcholine↗

Voltage- and time-dependent potassium conductances enhance the frequency response of horizontal cells in the turtle retina.

The contribution of voltage- and time-dependent potassium conductances to visual information processing in the distal turtle retina was studied in the isolated retina preparation. The effects of specific potassium channel blockers; tetraethylammonium (TEA) and 4-aminopyridine (4-AP) on the membrane potential and photoresponses of L-cones and L-type horizontal cells were monitored with intracellular microelectrodes. Both drugs produced a large depolarization of the L-type horizontal cells though the effect of 4-AP was more transient than that of TEA. While TEA produced response augmentation associated with negligible changes in the kinetics of the photoresponses, 4-AP induced profound changes in response kinetics which were seen as an overshoot of the resting potential at stimulus offset and a pronounced slowing down in the return of the membrane potential toward the prestimulus level. The effects of TEA on horizontal cells could be accounted for by the action of the drug on cone photoreceptors. The effects of 4-AP on the horizontal cells could not be attributed to an indirect action mediated by either the cone photoreceptors or by GABAergic and/or glycinergic neurons in the inner retina. These results suggest that voltage- and time-dependent potassium conductances act to speed up the recovery of the turtle horizontal cell membrane potential from the effects of bright light stimuli. Such a role was supported by the effects of potassium channel blockers on the frequency response curves of horizontal cells: the corner frequency was reduced on the average by 25%.

4-Aminopyridine↗

Morphogenesis of the cranial segments and distribution of neural crest in the embryos of the snapping turtle, Chelydra serpentina.

Recent studies of the heads of vertebrates have shown a primitive pattern of segmentation in the mesoderm and neural plate not previously recognized. The role of this pattern in the subsequent distribution of cranial crest and the development of branchial arches and cranial nerves, may resolve century-old arguments about the evolution of vertebrate segmentation. In this study, we examine the early embryonic development of the cranium of a primitive amniote, the snapping turtle, with the SEM. We show that the paraxial mesoderm cranial to the first-formed somites is segmented and that this pattern is based on somitomeres, similar to those described in the embryos of chick and mouse. Seven contiguous pairs of somitomeres comprise the "head mesoderm"; the first pair of somites actually arise from the eighth pair of somitomeres added to the axis. Cranial somitomeres are associated with specific brain regions, in that the first pair lie adjacent to prosencephalon, the second and third pair are adjacent to the mesencephalon, and the fourth, fifth, sixth, and seventh pair of somitomeres lie adjacent to individual neuromeres of the rhombencephalon. Prior to the closure of the anterior neuropore, cranial neural crest cells first emerge from the mesencephalon and migrate onto the second and third somitomeres. Shortly thereafter, neural crest cells emerge at more caudal levels of the rhombencephalon, beginning at the juncture of the fifth and sixth somitomeres. Eventually, neural crest originating from the mesencephalon spreads caudally as far as the fourth somitomere, leaving a gap in crest emigration adjacent to the fifth somitomere. The otic placode develops from the surface ectoderm covering the sixth and seventh somitomeres, and the adjacent rhombencephalic neural crest moves around the cranial and caudal edge of the placode. At more caudal levels, rhombencephalic crest cells merge with cervical crest populations to form a continuous sheet over the somites. By the time the anterior neuropore closes, some of the mesencephalic crest cells return from the paraxial mesoderm to spread onto the rostral wall of the optic vesicle and future telencephalon. The segmentation of the mesoderm and patterned distribution of cranial neural crest seen in snapping turtle embryos, further strengthens the argument that the heads of amniotes are derived from a common metameric pattern established early during gastrulation.

Animals↗

Localization of 2-[125I]iodomelatonin binding sites in visual areas of the turtle brain.

The hormone melatonin is believed to play an important role in the regulation of both circadian and circannual rhythms. In mammalian vertebrates melatonin receptors are discretely localized, with broader distributions reported in avians and reptiles. To examine the sites at which melatonin may act in the turtle brain, 2-[125I]iodomelatonin binding sites were assessed using quantitative autoradiography. Specific binding sites were primarily restricted to forebrain structures with a wide distribution in visual recipient areas. The distribution of melatonin sensitive sites within the turtle visual system suggests that the ability to transduce received photoperiodic signals in the reptilian brain is broadly distributed within the central nervous system.

Animals↗

Monoclonal antibody labels both rod and cone outer segments of turtle photoreceptors.

We have studied the immunoreactivity of turtle photoreceptors to a monoclonal antibody (MAb 15-18) which binds to the external loop connecting bovine rhodopsin helices IV-V. Three chromatic types of cone photoreceptors were identified by the presence and color of oil droplets. MAb 15-18 intensely labeled the outer segments of both rods and green cones. In addition, a weak cross-reactivity was also found in the outer segments of red cones having a pale-green oil droplet, and of blue cones. Other morphological subtypes of red cones, cones with a red oil droplet and both members of double cones, showed no labeling. Our results indicate that rhodopsin and green cone opsin have a similar antigenic determinant, and that two different structural forms of red cone opsin may be present in the turtle retina.

Animals↗

Immunocytochemical demonstration of astrocytes in the eighth cranial nerve of the red-eared turtle.

Coronal sections through the eighth cranial nerve and medulla of the red-eared turtle were immunocytochemically stained for the astrocytic intermediate filament protein, glial fibrillary acidic protein. Reaction product appeared in the medial one-third of the eighth cranial nerve fibers as they penetrated the medulla. The remaining two-thirds of the nerve did not show any staining for glial fibrillary acidic protein. The lateral aspect of the nerve corresponds with the extracranial portion of the nerve. When the eighth cranial nerve of the turtle has been transected extracranially it still regenerates into the cochlear nuclei. Results of the present study indicate that the eighth cranial nerve was transected in earlier studies in a region devoid of astrocytes.

Animals↗

Comparison of the structure of turtle pancreatic ribonuclease with those of mammalian ribonucleases.

There are 33 invariant amino acid positions out of 132 positions in 42 investigated sequences of ribonucleases from a number of mammalian species and a reptile (snapping turtle, Chelydra serpentina). These invariant residues are unequally distributed over 3 different parts of the molecule. The lobe of the S-protein part of the molecule, which lacks one disulfide bridge and has two shortened loops in turtle ribonuclease, has the lowest percentage of invariant residues, although the active-site residue His 119 is located in this part.

Amino Acid Sequence↗

In vivo and in vitro responses to gonadotropin releasing hormone in the turtle, Chrysemys picta, in relation to sex and reproductive stage.

In vivo and in vitro responsiveness to gonadotropin releasing hormone (GnRH) was studied in the turtle, Chrysemys picta, after manipulation of reproductive condition by temperature: Warm temperatures (28 degrees) induced testicular growth and ovarian regression compared to cold (17 degrees) treatment. Only males (and primarily from cold treatment) responded to GnRH injection (40 micrograms/100 g body wt intracardiac); correlated increases occurred in plasma LH and testosterone. Effects of GnRH (10 and 100 ng/ml) on LH and FSH secretion by hemipituitaries were studied in a superfusion system; tissues responded to between 0.1 and 1 ng/ml GnRH. Sex differences were evident in both acute and chronic effects of GnRH. Although both groups of females had significantly (sixfold) higher pituitary LH content, basal secretion rates of gonadotropins were similar, and LH and FSH secretion in males was more responsive to GnRH. Gonadotropin secretion rates by male glands showed high initial increments (approx four- to sevenfold) followed by an attenuation (especially LH) during 5 hr of GnRH superfusion. In contrast, tissues from warm-treated females showed a smaller initial response (approx twofold) followed by a progressive increase in output over time, and glands from cold-treated females did not respond to GnRH. Total LH secretion by superfused male hemiglands represented almost half the total LH recovered (secreted + stored); whereas, females secreted only 5% ("cold-treated") or 10% ("warm-treated") of total LH. Thus, the capacity of the pituitary to respond to GnRH is influenced by both sex and reproductive condition in the turtle. Secretion of both FSH and LH were similarly stimulated by GnRH, but thyrotropin (TSH) secretion was independent of GnRH.

Animals↗

Specific uptake, dissociation, and degradation of 125I-labeled insulin in isolated turtle (Chrysemys dorbigni) thyroid glands.

Thyroid glands from turtles (Chrysemys dorbigni) pretreated with potassium iodide were incubated with 125I-insulin in the presence or absence of unlabeled insulin, in order to study its specific uptake. At 24 degrees, the specific uptake reached a plateau at 180 min of incubation. The dose of bovine insulin that inhibited 50% of the 125I-insulin uptake was 2 micrograms/ml of incubation medium. Most of the radioactive material (71%) extracted from the gland, after 30 min incubation with 125I-insulin, eluted in the same position as labeled insulin on Sephadex G-50. Only 24% eluted in the salt position. After 240 min incubation, increased amount of radioactivity appeared in the Na125I position. When bovine insulin was added together with the labeled hormone, a substantial reduction of radioactivity was observed in the insulin and Na125I elution positions. Dissociation studies were performed at 6 degrees in glands preincubated with 125I-insulin either at 24 or 6 degrees. The percentage of trichloroacetic acid (TCA)-soluble radioactive material in the dissociation medium increased with incubation time at both temperatures. However, the degradation activity was lower at 6 than at 24 degrees. The addition of bovine insulin to the incubation buffer containing 125I-insulin reduced the radioactive degradation products in the dissociated medium. Chloroquine or bacitracin inhibited the degradation activity. Incubation of thyroid glands with 125I-hGH or 125I-BSA showed values of uptake, dissociation, and degradation similar to those experiments in which an excess of bovine insulin was added together with the labeled hormone. Thus, by multiple criteria, such as specific uptake, dissociation, and degradation, the presence of insulin-binding sites in the turtle thyroid gland may be suggested.

Animals↗

Seasonal cycles in testicular activity, gonadotropin, and thyroxine in the painted turtle, Chrysemys picta, under natural conditions.

Plasma levels of testosterone (T), thyroxine (T4) and follicle-stimulating hormone (FSH) were measured in a field population of the painted turtle, Chrysemys picta, in Michigan. All three hormones showed pronounced seasonality; plasma luteinizing hormone (LH) remained nondetectable. Plasma T and FSH concentrations were highly correlated and exhibited biphasic cycles with peaks in spring and fall, whereas T4 showed a single peak in summer, coincident with the nadir in T. Hormone levels were minimal on the day that animals emerged from hibernation at the end of March; T and FSH then increased rapidly (in ca. 1 week after emergence) to a transient peak that persisted for only ca. 2 weeks. Plasma T and FSH rose again in September before the onset of hibernation and shortly after the late summer peak in spermatogenetic recrudescence. Plasma T4 increased more gradually after emergence in spring and did not peak for 1-2 months, coincident with the nadir in T. The profile in plasma FSH is consistent with the view that this gonadotropin may regulate androgen secretion but it did not show the expected relationship to the spermatogenetic cycle. Separate studies indicated that the turtles are sensitive to capture and handling; hormone levels (especially androgen) fall precipitously within a day of capture. These "stress" effects may account for discrepancies with previous studies of plasma T in this species.

Analysis of Variance↗