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Paraventricular nucleus (nucleus paraventricularis) and supraoptic nucleus (nucleus supraopticuś) in spiny mouse (Acomys cahirinus Desmarest, 1891) - Biblioteka UMCS

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A N N A L E S

U N I V E R S IT A T 1 S M A R I A E C U R I E - S K Ł O D O W S K A L U B L I N - P O L O N I A

VOL. LV SECTIO C 2000

*lnsiitule o f Animal Anatomy, Univcrsity o f Agricullure, Lublin lnstilute o f Biology UMCS

Department o f Comparative Anatomy and Anthropology

M A REK JA STRZĘB SK I* ZO FIA SK RZY PIEC

Paraventricular nucleus (nucleus paraventriculariś) and supraoptic nucleus (nucleus supraopticuś) in spiny mouse (Acomys cahirinus D e s m a re s t, 1891)

Jądro przykomorowe (nucleus paraventriculariś) i jądro nadwzrokowe (nucleus supraopticuś) u myszy Acomys cahirinus D e s m a re s t, 1981)

Paraventricular nucleus (nucleus paraventricularis) and supraoptic nucleus (nucleus supraopticuś) m ake com ponents ofm acrocellular neurosecretory system of the hypothalam us (16). They form so called hypothalam ic - hypophysial system together with nervous lobe of the hypophysis, the system that regulates water balance and tem peraturę of an organism. Some laboratory animals subjected to a therm al shock showed significant changes in the cełls of the m entioned nucłei (6, 7, 8). The earlier examinations on the m orphology of the neurosecretory nuclei have also dem onstrated m orphological changes in many species ofm am m als, both laboratory (1 ,2 ,4 , 10, 15, 16, 18) and domestic (5, 19, 20) as well as free living ones (9, 11, 13, 14, 17). The elear differences in size and dism em berm ent of these nuclei was stated, particularly of the paraventricular nucleus, in gopher (Spermophilus suslicus) and dormouse (Muscardinus avel- lanarius) (11). There were also investigations on the development of ultrastruc- ture of supraoptic nucleus cells in rat (2).

The observations presented below concern a species Acomys cahirinus

(Muridae), a rodent living in the semidesert regions of the eastern part of the

M editerranean region. A climate of the region, especially very high differences

between a night and day tem peraturę, does affect the hypothalamic-hypophysial

system. M onitoring the m orphology and a degree of the paraventricular and

supraoptic nucleus developm ent in spiny m ouse seems to be advisable, in

particular in com parison to these species examined that live in the tem perate

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14

MAREK JASTRZĘBSKI, ZOFIA SKRZYPIEC

climate conditions. M oreover, the authors of the present article hołd this belief for recently num erous studies have been m adę on the usage of water contained in food as well as water balance of species living in the desert and semidesert regions (3, 12,21).

MATERIAŁ ANO METHODOLOGY

Theexaminations were conducled on Ihe brains ofsexually maturę males and females (two brains of each sex) bred in Dept. of Comparative Anatomy and Anthropology UMCS. The materiał was fixed in formalin and then, having undergone the alcoholic series of inereasing concentration, it was paraffin embedded. The serial transverse sections of 10 pm thickness were stained with cresyl violet for celi presence according to Kluver and Barrera’s melhod.

RESULTS ANO OISCUSS1ON

P a r a v e n t r i c u l a r n u c l e u s (nucleus paraventricularis)

Paraventricular nucleus (PVN) is a very short and not differentiated band of nervous cells in this species. It is found (like in other species) near the dorsal region of ventricle III, in sonie places a little over its lumen. The posterior pole PVN lies in the transverse piane found in half of the supraoptic nucleus length, the anterior one is very unclear, yet its forward rangę is smaller than that of the anterior pole of supraoptic nucleus (SON). The posterior segment PVN is a narrow, not differentiated tract of closely arranged cells. Its transverse cross-sections are rounded and, moving forward, they become vertical and oval.

The anterior half of the nucleus is substantially thicker (about twice), vertical and oval. Alike the posterior part, the cells are spaced closely. A region taken by PVN is a bit protruded dorsally over the lumen of ventricle III (Phot. 1).

The cells form ing PVN are mainly m ultipolar of 6 up to 10 pm (Phot. 4). The rounded and spindle-shaped cells (up to 40 gm long) are quite fewer. Celi nuclei are usually big with well stained nuclear membranę. The cells are fdled with m icrogranular or shapeless tigroid.

S u p r a o p t i c n u c l e u s (nucleus supraopticus)

This nucleus (SON) is well developed. The posterior segment, about 1/3 of

nucleus length, is a vertical, rather narrow band found laterally of tractus opticus

(Phot. 2). M oving forw ard, the transverse cross-sections of the nucleus enlarge

and take shape of a not very thick band that surrounds tractus opticus in an

arch-like way on the lateral side (Phot. 3). In this part, the SON forming cells are

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PARAVENTRICULAR NUCLEUS (N UCLEUS PARAUENTRICULARIS) A ND SUPRAOPTIC NUCLEUS... 1 5

arranged very closely. From about half of the length, the transverse cross- -sections o f the nucleus grow smaller. The portion that lies laterally of tractus opticus is evidently narrow er than this found over the tract. A short anterior segment m akes a narrow unclear band of cells loosely spaced over the optic tract.

The cells forming the supraoptic nucleus reach the size of 10 to 20 gm (Phot. 5). These are spindle-shaped, m ultipolar and rounded cells that stain intensively. Quite typical are great celi nuclei with very distinct nuclear membranę. Some cells show clusters of nuclear chrom atin near the nuclear membranę.

Com paring the m orphology of supraoptic and paraventricular nucleus in Acomys cahirinus and some other rodents, it can be stated that there is a very significant difference in the structure of paraventricular nucleus. it is a poorly developed single tract of cells, while in dormouse and gopher to even greater extcnt, it is a big dismembered cluster of nervous cells with differentiated shapes.

There occur rounded, m ultipolar and spindle-shaped cells, whereas in Acomys cahirinus m ultipolar cells predom inate. Taking into consideration a position of paraventricular nucleus in a species studied, it corresponds to a paramedial part of the nucleus in a gopher, dorm ouse and rat Wistar. It is also of a shape resembling an elongated upturned drop and the contour of both paraventricular nuclei (the left and right side) looks like a letter “ V” . The appearance of the other parts PVN - la te ra l portion, dorsom edial cap as well as the posterior part cannot be stated.

The supraoptic nucleus in Acomys cahirinus has a structure approxim ating that of nucleus in gopher and dormouse. In case of rat the differences are also minimal and they refer m ainly to the size, not a position. A caudal segment of the supraoptic nucleus that lies laterally of tractus opticus corresponds to pars tuberalis distinguished by Arm strong et al. (1) in W istar rat, gopher and dormouse (11). A part placed dorsally of tractus opticus may be considered an equivalent of pars anterior in the species mentioned.

In gopher, dorm ouse and rat in particular, both portions of the supraoptic nucleus are clearly separated from each other. However, in Acowrys cahirinus a portion that can be regarded as an equivalent of pars tuberalis is connected with pars anterior and m akes a narrow band of nervous cells placed over the lateral portion of optic nerve chiasm. Pars tuberalis of the described species is morę poorly developed in com parison with gopher and dormouse.

In this case the m orphological examinations cannot be any foundations for drawing conclusions on the relation between the development degree of neurosecretory centres discussed and the conditions of animal life. The m acrocellular neurosecretory nuclei developed best are recorded in rat (1, 16).

A little poorer developm ent of these centres is noted in gopher and dormouse

(11), whereas the poorest development of neurosecretory nuclei - in Acomys

cahirinus, the paraventricular nucleus in particular. This nucleus is m adę of

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16

M AREK JASTRZĘBSKI, ZOFIA SKRZYPIEC

hom ogenous, not differentiated band of cells. A degree of supraoptic nucleus deveiopment in all the m entioned species of rodents is congenial, still some differences occur. The m ost distinct division into two portions - pars anterior and pars tuberalis appears in rat, while the least elear one in Acomys cahirinus.

The course of life of the rodents mentioned as well as their environment are absolutely unlike. R at is active all the year long and adapted perfectly to living in any conditions i.e. in basement, ditches, farm buildings. Hence, an ambient tem peraturę and m oisture are different and changeable. Gopher and dormouse are hibernating animals whose body tem peraturę goes down to a few grades over the dorm ancy time and the ratę o f their all m etabolic processes decreases to minimum. The changes take place in a year cycle. The animals living in the semidesert regions o f the eastern part of M editerranean are exposed to quite considerable tem perture fluctuations in a 24 hrs cycle. That is why, the water balance of these species, in that spiny mouse, has to be very economical, regarding this climate dryness, too. K am and D e g e n (12) hołd a belief that the water contained in plant and animal feed (snails mainly) is sufficient for an animal.

The m orphology of supraoptic nucleus and paraventricular one in Acomys cahirinus is evidently simpler than in rat, gopher and dormouse. A question arises if this State of things is a m atter of specialization, adaptation to the changes of therm al conditions occurring in a very wide but permanent rangę and reoccurring at some regular, relatively short time intervals. The domestic species under investigation meet with frequent irregular changes in tem peraturę and m oisture which m ake an organism adapt perm anently to some exogenous

changes appearing in their environment.

REFERENCES

1. A r m s tr o n g W. E ., W a ra c h S ., H a tt o n G . I ., M c N e ill T. H .: Subnuclei in the rat hypothalamic paraventricular nucleus: A cytoarchitectonic, HRP and immunocytochemical analysis. Neurosci. 5, 1931-1956 (1980).

2. D a ik o k u S ., S a lo T . J. A ., H a s h im o to T ., M o r is h it a H .: Development of the ultrastructures of the median and supraoptic nuclei in rats. Tokushima J. Exp. Med. 15, 1-15 (1968).

3. D e g e n A. A ., K a m M Water intake in two coexistingdesert rodents, Acomys cahirinus and Gerbillus dasyurus. J. Mammal. 73, 201-206 (1992).

4. F e lle n D . L ., C a s h n e r K . A .: Cytoarchitecture of the supraoptic nucleus. Neuroendoc- rinol. 29, 221-230 (1979).

5. G a d a m s k i R ., Ł a k o m y M .: The nuclei of the anterior part of the hypothalamus of the cow.

J. Himforsch. 1/2, 27-41 (1973).

6. G a jk o w s k a B .: Badania ultrastrukturalne układu podwzgórzowo-przysadkowego mózgu szczura w stresie hypotermicznym. Neuropat. Pol. 19, 21-31 (1981).

7. G a jk o w s k a B.: Badania mikroskopowo-elektronowe jądra nadwzrokowego i jądra przyko-

morowego w przedłużającym się stresie hipertermicznym. Neuropat. Pol. 24, 417429 (1985).

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ANN. UNIV. MARIAE CURIE-SKŁODOWSKA, sectio C, vol. LV Tabl. I

Marek Jastrzębski, Zofia Skrzypiec

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ANN. UNIV. MARIAE CURIE-SKLODOWSKA, sectio C, vol. LV Tabl. II

Marek Jastrzębski, Zoiia Skrzypiec

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PARAVENTR1CULAR NUC LEU S (N U C LE U S PARAEENTRICULARIS) A N D SUPRAOPTIC NUCLEUS...

17

8. G a jk o w s k a B ., L o e sc h A ., P lu ta R .:T h e effect of high ambient temperatures on the hypothalamo-neurohypophysial system of the rabbit. I. The supraoptic and paraventricular nuclei. Neuropat. Pol. 23, 55-69 (1985).

9. G a l e r t D .: The supraoptic and paraventricular nuclei in insectivores. Folia Morphol. (Warsz.) 45, 182-191 (1986).

10. G a l a s i ń s k a - P o m y k o ł I ., M a rc in k ie w ic z D .: Morfologia ośrodków neurosekrecyjnych podwzgórza królika. Folia Morphol. (Warsz.) 31, 385-393 (1972).

11. J a s t r z ę b s k i M ., S k rz y p ie c Z .: Structure and topography of paraventricular nucleus (nucleusparaventricularis) and supraoptic nucleus (nucleussupraopticus)'m gopher (Spermophilus .su.r/icu.rG ii ld.) and dormouse (Muscardinusavellanarius L.). Ann. Univ. Mariae Curie-Sklodowska,

sectio C 52, 111-117 (1997).

12. K am M ., D e g e n A. A .: Diet selection and energy and water budgets of the common spiny ntouse Acomys cahirinus. J. Zool. 225, 285-292 (1991).

13. K o ła c z k o w s k i J . , W e n d e r M .: Cytoarchitektonika pola przedwzrokowego i podwzgórza susla. Folia Morphol. (Warsz.) 8, 1-14 (1957).

14. R o b a k A ., S z te y n S .: The topography and cytoarchitectonics of the nuclei of supraoptic and praeoptic areas of insectivores. Folia Morphol. (Warsz.) 48, 210-218 (1989).

15. S ilv e rm a n A. J .: Magnocellular neurosecretory system. Ann. Rev. Neurosci. 6, 375-380 (1983).

16. S i l v e r m a n A . J . , P i c k a r d G . E . : TheHypothalamus. In: ChemicalNeuroanatomy. lid. P.

C. Emson, Raven Press, New York 1983.

17. S iu d a S.: Comparative studies on the neurosecretory system of some species of voles. Acta Theriol. 23, 435442 (1978).

18. V a n d e s a n d e F ., D ie r ic k x K .: Identification of the vasopressin producing and of the oxytocin producing neurons in the hypothalamic magnocellular neurosecretory system of the rat.

Celi Tiss. Res. 164, 153-162 (1975).

19. W e le n to J .: Budowa i topografia jąder międzymózgowia świni. Ann. Univ. Mariae Curie-Sklodowska, sectio DD. 19, 125-188 (1964).

20. W e le n to J ., S z te y n S ., M il a r t Z . : Observations on the stereotaxic configuration of the hypothalamus nuclei in the sheep. Anat. Anz. 124, 1-27 (1969).

21. W e is s e n b e rg S ., S h k o ln ik A .: Melabolic ratę and water economy in the desert and Mediterranean populations of the common spiny mouse (Acomys cahirinus') in Israel. Isr. J. Zool.

40, 135-143 (1994).

PHOTOGRAMS

Phot. 1. Paraventricular nucleus - transverse cross-section in half of the length. Mag. 60 x . Phot. 2. Supraoptic nucleus - pars tuberalis. Mag. 60 x .

Phot. 3. Supraoptic nucleus - pars anterior. Mag. 60 x . Phot. 4. Cells of paraventricular nucleus. Mag. 500 x . Phot. 5. Cells of supraoptic nucleus. Mag. 500 x .

ABBREV1ATIONS USED

P - paraventicular nucleus, Sa - supraoptic nucleus pars anterior, St - supraoptic nucleus pars

tuberalis, to - tractus opticus.

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MAREK JASTRZĘBSKI, ZOFIA SKRZYPIEC

STRESZCZENIE

Opisano morfologię jądra przykomorowego (nucleus paravenlricularis( i jądra nad wzrokowego

(nucleus supraopticus} u myszy kolczystej (Acomys cahirinus D e s m a r e s t 1891) na podstawie

obserwacji seryjnych skrawków parafinowych barwionych fioletem krezylowym wg metody KJiivera

i Barrery. Do badań użyto po dwa mózgowia - samca i samicy. Jądro nadwzrokowe jest

wydłużonym, pojedynczym pasmem komórek nerwowych. W porównaniu z innymi gatunkami

gryzoni odpowiada ono części przyśrodkowej tego jądra (wg Armstronga). Jądro przykomorowc

u myszy kolczystej wykazuje też mniej zróżnicowaną budowę komórkową: występują tu głównie

komórki wielobiegunowe. Jądro nadwzrokowe ma budowę podobną jak u susła peretkowanego

i orzesznicy, a także zbliżoną do budowy tego jądra u szczura Wistar, chociaż podział na pars (interior

i pars tuberalis, które wyróżniane są u szczura, nie jest tak wyraźny.

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