Research Article (Open access) |
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ABSTRACT- Reproduction is a vital process provided to all living individuals by the nature itself to reproduce their
similar one after death. Channa gachua is used due to easily throughout year availability. Male gonad was removed during
different reproductive phases. The nourishing protein contain was recorded by Lowry’s method 660nm during matured
male gonad as 0.555 mg/ml. Sertoli cells were observed on their development and parameters were recorded with the help
of phase contrast microscope (Phase contrast-Olympus) as total number of Sertoli cells 150±199 in number, diameter of
the cell 0.1±0.2m perimeter of the Sertoli Cell 0.1 to 0.01m in matured testis on the colour intensity. Same conditions
were used to abnormal male brooder in hatchery the nourishing protein contain was comparatively low about infertile
male brooder in matured gonad as 0.467mg/ml. The development of Sertoli cell and its parameter were comparatively low
as number of Sertoli cells 99±120, diameter of the cell 0.001±0.005m perimeter of the Sertoli Cell in male brooder. The
lesser development of sertoli cell leads to improper development of Sertoli gives insufficient sperms cell count for
abnormal fertilization.
Key words- Testis, Ovary, Reproduction, Reproductive phases, Supportive cells, Channa gachua
INTRODUCTION
Reproduction is a vital process provided to all living
individuals by the nature itself to reproduce their similar
one after death. Channa gachua is used due to easily
throughout year availability. Channa gachua is having
important as much as Indian major carps. It is a good
brooder used in induced breeding process in Chinese
hatchery and to bring perceptual breeding in it. Reproductions
in any animals are one of the basic functions to
propagate the respective population in cyclic manner.
Fishes has got a complicated reproductive behavior very
typical embryonic development. Morphologically, healthy
testis consists of different organells with the cells lie Sertoli
and Leydig’s cells which are really a supportive and
functional unit of gonads.
The somatic Sertoli cell in fishes plays an essential role in
embryonic determination of a male somatic sex and
spermatogenesis during adult life. One individual Sertoli
cell sullies a clone of developing germ cells with nutrient
and growth factors and it is well established that the
number of Sertoli cell. The testes of teleost fishes show
greater morphological variation than in other vertebrates
[1-3]. In most cases, testes are a pair of elongated structures
composed of branching seminiferous tubules embedded in
the stroma. The testis consists of thin-walled tubules or
lobules that contain germ cells - the spermatogonia- which
are endodermal in origin. Germ cells divide in clusters
enclosed by a cyst. Primary spermatogonia - the stem cells
- which are present throughout the year, divide mitotically
to give rise to secondary spermatogonia which get
transformed into primary spermatocytes. They divide by
meiosis and give rise to spermatids from which
spermatozoa are formed. The seminiferous tubules are
packed with spermatozoa in the pro-spawning and
spawning periods. Vertebrate testis shows a germinal
compartment represented by seminiferous tubules
(seminiferous lobules), in which two cell types are found:
somatic and germinal. Compared to mammals, Sertoli cell
supporting capacity in the teleost Nile tilapia is remarkably
high [4]. The number of mitotic divisions during
spermatogenesis to form primary spermatocytes is also
species-specific Schulz et.al. (2002). In mammals, the ratio
germinal cells: A Sertoli cell (which expresses the Sertoli
cell supporting capacity) is relatively defined for each
species [5-7].
MATERIAL AND METHOD
Channa gachua was used for male gonadal study and
collected from Godavary River near Aurangabad. Fish was
dissected and gonad removed, fixed with help of formal
solution as fixative.
The nourishing protein contain was measured by Lowry’s
method 660nm during matured male gonad. Sertoli cells
were observed on their development and parameters were
recorded with the help of phase contrast microscope (Phase
contrast-Olympus). Staining of the section made with
reagents Haematoxyline and Eosin.
RESULT AND DISCUSSION
Male gonad was removed during different reproductive
phases. The nourishing protein contain was recorded by
Lowry’s method 660nm during matured male gonad as
0.555 mg/ml. Sertoli cells were observed on their
development and parameters were recorded with the help
of phase contrast microscope (Phase contrast-Olympus) as
total number of Sertoli cells 150±199 in number, diameter
of the cell 0.1±0.2m perimeter of the Sertoli Cell 0.1 to
0.01m in matured testis on the colour intensity.
Same conditions were used to abnormal male brooder in
hatchery the nourishing protein contain was comparatively
low about infertile male brooder in matured gonad as
0.467mg/ml.The development of Sertoli cell and its
parameter were comparatively low as number of Sertoli
cells 99±120, diameter of the cell 0.001±0.005m
perimeter of the Sertoli Cell in male brooder. The lesser
development of sertoli cell leads to improper development
of Sertoli gives insufficient spem cell count for abnormal
fertilization.
                       
                                
Photo 1. Testis in growing phase
                                                                                        
Photo 3 - Matured testis phase position
in
                                                                                                                                                                                              
Channa gachua (Ham-1822)
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